The bone marrow is home to well-balanced normal hematopoiesis, but also the stage of leukemia’s crime. Marrow adipose tissue (MAT) is a unique and versatile component of the bone marrow niche. While the importance of MAT for bone health has long been recognized, its complex role in hematopoiesis has only recently gained attention. In this review article we summarize recent conceptual advances in the field of MAT research and how these developments impact our understanding of MAT regulation of hematopoiesis. Elucidating routes of interaction and regulation between MAT and cells of the hematopoietic system are essential to pinpoint vulnerable processes resulting in malignant transformation. The concept of white adipose tissue contributing to cancer development and progression on the cellular, metabolic, and systemic level is generally accepted. The role of MAT in malignant hematopoiesis, however, is controversial. MAT is very sensitive to changes in the patient’s metabolic status hampering a clear definition of its role in different clinical situations. Here, we discuss future directions for leukemia research in the context of metabolism-induced modifications of MAT and other adipose tissues and how this might impact on leukemia cell survival, proliferation, and antileukemic therapy.
The bone marrow microenvironment (BMM) is characterized by a complex network of different cell types providing key signaling events for the regulation of hematopoiesis. Although leukemia is caused by a series of genetic hits to hematopoietic stem and progenitor cells leading to malignant transformation [1,2,3], evidence is accumulating that the BMM also influences development and progression of malignancies in the bone marrow (BM). Alterations in niche cells may also contribute to leukemogenesis. For example, deletion of Dicer1, the key factor of microRNA maturation in osteoprogenitors, but not in mature osteoblasts, led to disruption of hematopoietic integrity and resulted in myelodysplasia and emergence of acute myelogenous leukemia (AML) in mice . Furthermore, the local environment in the BM is also crucial for leukemia cell survival and might play a role in resistance to chemotherapy and disease relapse. A prominent example for interaction of leukemic cells with their surroundings is the CXC motif ligand 12 and CXC chemokine receptor 4 (CXCL12/CXCR4) axis . The chemokine CXCL12 is secreted by BM stromal cells and serves as a potent chemo-attractant for CXCR4-positive hematopoietic cells, withholding them in an environment equipped with growth factors essential for their survival. This mechanism can be hijacked by AML cells, which also express CXCR4 . On these grounds, the concept of inhibition of the leukemia–niche interaction was developed as novel therapeutic strategy. Indeed, targeting the CXCL12/CXCR4 axis appears to deliver the promising results in early-phase clinical trials , and it is expected that additional routes of interaction between leukemia and the BMM will be discovered. Interestingly, a prominent cell type within the BMM has long been neglected and only recently entered center stage: the BM adipocyte. Adipocytes are highly active secretory cells. Via their secretion products, which are collectively referred to as adipokines, they contribute to the development and progression of solid tumors, which are surrounded by adipose tissue (AT) . There is accumulating evidence that they might play a similar role in the context of leukemia in the local BMM but also systemically via endocrine routes of interaction.
The colors of fat—white, brown, beige, pink, and yellow
When talking about AT, we usually refer to the two classical types, i.e., white adipose tissue (WAT) and brown adipose tissue (BAT) (Fig. 1). WAT covers the human body in a subcutaneous layer but also surrounds the inner organs in visceral depots, thereby providing insulation and protection . It serves as an endocrine organ regulating processes as important as hunger and satiety, energy and glucose homeostasis, and hemostasis but its best-known function is storage of surplus energy in form of triglycerides, which can again be released in case of higher demand or food shortage .
BAT, instead of saving fat, has the unique capability of using up stored triglycerides for production of heat in a process called nonshivering thermogenesis . This process is mediated by uncoupling protein-1 (UCP1), which is located at the inner mitochondrial membrane of brown adipocytes and, nomen est omen, uncouples the oxidative phosphorylation from the ATP-synthase to generate heat instead of ATP . The brown color results from high amounts of cytochrome C in this mitochondria-rich tissue.
Beige (brite, inducible BAT-like) adipocytes can arise within WAT depots upon chronic cold exposure (reviewed in ) (Fig. 1). They represent an intermediate, bifunctional phenotype of adipocytes, which stores triglycerides and also contributes to heat production via upregulation of UCP1 . In rodents, beige AT is responsible for the maintenance of body temperature during cold temperatures . Pink AT evolves during pregnancy and lactation from WAT via transdifferentiation, consists of milk-secreting alveolar cells and appears pink in color (review in ) (Fig. 1). Among these four types, only WAT has been linked to extramedullary hematopoiesis as well as leukemia cell biology as described below.
The color yellow was assigned to marrow adipose tissue (MAT) (Fig. 1). In a healthy, lean person, MAT represents over 10% of total fat mass . Although adipocytes of the BM resemble the white adipocyte’s unilocular morphology, they display a distinct gene expression , lipid profile [14, 15] and metabolism, e.g., seem to be resistant to calorie restriction-induced hydrolysis of stored triglycerides .
Our bones are full of fat—but why?
The bone cavity formed by osteoblasts harbors the BM and is home to hematopoiesis (Fig. 2a) maintained by hematopoietic stem cells (HSCs). HSCs have two essential features: they possess (1) self-renewal activity and (2) multipotency, i.e., they are able to differentiate into all mature blood cells . Common myeloid progenitors or common lymphoid progenitors give rise to cells from either the myeloid lineage, which include monocytes, granulocytes, erythrocytes, and platelets or from the lymphoid lineage, i.e., B cells, T cells, or NK cells, respectively (Fig. 2b). The BM comprises MSCs that can further differentiate into other cell types, e.g., adipocytes, osteoblasts, chondrocytes, and myocytes  but also fibroblasts  and components of the nervous system  (Fig. 2c). Whether MSCs can also give rise to endothelial cells is still controversially discussed .
Recently, the murine BM was analyzed by single-cell RNA-sequencing (scRNA-seq) either under normal or stressed conditions  or in the context of AML . Both studies report a dynamic cellular heterogeneity of the niche and an impressive plasticity in response to exogenous stimuli.
HSCs critically depend on factors provided by the BMM such as stem cell factor (SCF) and CXCL12 [23,24,25]. Perivascular stromal cells, also known as CAR (CXCL12-abundant reticular) cells, are the main source of CXCL12 , but it is also expressed in endothelial cells and osteoblasts, albeit at lower levels . Perivascular stromal cells and endothelial cells are crucial components of the HSC niche, which is highlighted by the fact that both cell types secrete SCF . Moreover, BM adipocytes are also a major supplier of SCF  and a study in mice with an adipocyte-specific knockout revealed that MAT-derived SCF is essential for hematopoiesis both under steady state and metabolic stress conditions .
HSCs reside in special “niches” in which their self-renewal and differentiation are influenced by signals from the surrounding BMM, a concept dating back to 1978 . Most HSCs reside close to vessels in the BM, i.e., 80% of HSCs around sinusoidal vessels (perisinusoidal), 10% around arterioles (periarteriolar), and another 10% close to transition zone vessels . Only a very small number of HSCs is located near the endosteum [29, 31] and osteoblasts are not required for HSC maintenance . Thus, the previously proposed model of an osteoblastic or endosteal HSC niche [33, 34] appears to be outdated .
In utero and at the time of birth, the bone cavities are predominantly occupied by hematopoietic red marrow . The formation of MAT starts during childhood and it further increases with age in a defined spatio–temporal manner from distal to proximal (for review see ). By the age of 25 years ~50–70% of BM space is already occupied by adipocytes . It was proposed that adipocytes in the BM are adjacent to the endosteal surface in the metaphysis . More recent work shows that adipocytes are in close vicinity to the sinusoidal vasculature and sympathetically innervated . In addition, adipocytes are in contact with a subset of hematopoietic cells, e.g., cells of the myeloid and granulocyte lineage as well as erythroblast islands .
The existence of two different types of MAT was suggested already in 1976 . Recently, this concept has been brought back to life by Scheller et al. proposing the concept of regulated MAT (rMAT) and constitutive MAT (cMAT) . They demonstrated that rMAT presents as single adipocytes and is located in more proximal regions at sites of active hematopoiesis, whereas cMAT is found in distal bones with low numbers of hematopoietic cells interspersed within adipocytes . During childhood, cMAT develops earlier than rMAT  is more resilient to environmental and metabolic changes, and contains larger adipocytes, which differ in their gene expression and lipid composition from rMAT adipocytes .
For decades MAT was considered a mere filler of the otherwise empty BM space and we have just begun to understand that its function goes far beyond. Comparable to WAT, MAT was identified as an endocrine organ . BM adipocytes secrete leptin , a hormone involved in the central nervous regulation of body weight, puberty, and fertility , and adiponectin, a regulator of metabolism and systemic insulin sensitivity . Therefore, MAT might serve as an “integrator” of the systemic nutritional and metabolic state into hematopoiesis.
Interestingly, MAT increases under certain clinical conditions including osteoporosis [44, 45], ageing [41, 44], metabolic diseases such as obesity  and diabetes (reviewed in ), and, counterintuitively, also in patients with anorexia nervosa  and under caloric restriction , whereas exercise can lower the MAT volume . MAT also expands during therapeutic interventions, e.g., radiation , chemotherapy , and treatment with glucocorticoids [52, 53]. A massive decrease or loss of MAT seems to occur only under severe energy deprivation as observed in patients with late stage anorexia nervosa, leading to gelatinous transformation of the BM .
Taken together, MAT is characterized by a dynamic plasticity and region-specific differences. The large variety of influencing factors seem to hamper systematic investigations and may account for controversies found in the literature.
MAT in normal hematopoiesis
We are only beginning to understand the role of MAT in normal hematopoiesis. In a landmark paper, Naveiras et al. identified MAT as negative regulator of hematopoiesis . They showed that adipocyte-rich BM isolated from tail vertebrae had reduced numbers and frequencies of HSCs and short-term progenitors along with an impaired cycling capacity as compared with adipocyte-free thoracic vertebrae . To corroborate an inhibitory role of MAT on hematopoiesis in the BMM, a pharmacological approach to inhibit adipogenesis as well as a genetic approach using the “fatless” A-ZIP/F1 mouse model was chosen. Under both conditions, BM engraftment after irradiation was accelerated , and the similar results were obtained by another group . In addition, an increase in MAT observed during obesity or aging impaired hematopoiesis . Remarkably though, MAT seems to differentially regulate the function of short-term and long-term HSCs because HSCs isolated from adipocyte-rich regions showed a better long-term engraftment . This interesting finding was substantiated in a co-culture study of HSCs with primary human MSCs or MSC-derived adipocytes from the femoral head of patients undergoing hip surgery . Whereas HSCs were stably maintained during long-term ex vivo culture with MSCs, adipocytes first induced a decline but later again an increase in colony-forming units suggesting that BM-derived adipocytes may enhance long-term maintenance of HSCs .
MAT in malignant hematopoiesis
There is accumulating evidence that MAT also influences survival and proliferation of leukemic blasts. Decline of normal hematopoiesis during leukemia progression is a well-known phenomenon, but has only recently been attributed to a disturbance of MAT function by AML cells resulting in compromised myelo-erythropoiesis . In contrast to MAT's supportive function of normal hematopoiesis during leukemia, its role in leukemia development is controversial and might be lineage specific. Thus, MAT was found to negatively affect T-ALL proliferation in vitro and in vivo thereby mediating chemoresistance . On the other hand, MAT supported the survival and proliferation of AML blasts from patients  by hijacking the metabolism of adipocytes to induce free fatty acid release via activation of lipolysis . Mechanistically, fatty acid binding protein-4 (FABP4) was essential for proliferation of AML blasts in co-culture with adipocytes as its knockdown by shRNA prevented AML blast proliferation, and, in addition, increased survival of mice in a model of Hoxa9/Meis1-driven AML .
Caloric restriction is known to result in an increase of MAT . Interestingly, fasting or dietary restrictions improve the outcome of different cancer entities. A recent paper by Lu et al. demonstrates that this also applies to B-ALL and T-ALL, but not AML . Repeated cycles of 1 day fasting followed by 1 day of feeding shortly after transplantation of leukemia cells completely inhibited leukemia development in the N-Myc B-ALL model and massively decreased the leukemic burden in the Notch1 T-ALL model. Mechanistically, fasting led to an upregulation of Lepr expression and activation of the downstream signaling molecule PR/SET domain 1 in leukemic cells . In contrast, the dietary regime had no beneficial effect in the MLL-AF9 AML model. The authors speculate that AML cells have high basal expression levels of Lepr and might therefore be resistant to fasting-induced upregulation of this pathway. In ALL, fasting not only prevented leukemia development, but also resulted in differentiation and depletion of leukemic cells. Most importantly though, fasting also effectively inhibited the growth of human patient-derived B-ALL in a xenograft model and the expression of LEPR signaling-related genes was correlated to prognosis in pediatric pre-B-ALL . Clearly, these findings open up new therapeutic strategies for the treatment of ALL. It can be speculated that other fasting-responsive pathways are also major contributors, e.g., the IGF-1/IGF-1R growth hormone axis . The concept of treating leukemia by forcing terminal differentiation of the malignant cell instead of killing it was proposed 40 years ago (for review see ). The findings by Lu et al. encourage the revival of this old concept from a new perspective: “starving leukemia to induce differentiation” .
Influence of other fat depots on normal and malignant hematopoiesis
Back in 1962, infiltrations of leukemia or lymphoma cells were identified in subcutaneous AT of patients . In mice, HSCs are not only found in the BM, but also in extramedullary gonadal WAT (gWAT) . gWAT represents the largest visceral fat depot in mice and was just recently identified as a reservoir of leukemic stem cells (LSCs) in a model of blast crisis chronic myeloid leukemia . The LSCs present in gWAT had a proinflammatory gene signature and induced lipolysis leading to atrophy of AT. Interestingly, fatty acid oxidation (FAO) was increased in leukemic versus nonleukemic cells, and LSCs presented with the highest FAO rate suggesting that these cells might benefit most from lipolysis. In line, the fatty acid transporter CD36 was highly, but not uniformly expressed in LSCs. Specifically, CD36 + LSCs were strikingly enriched in gWAT and were protected from chemotherapy by the local AT microenvironment. Vice versa, the knockout of CD36 decreased the leukemic burden in gWAT and sensitized LSCs to chemotherapy. Thus, LSCs may hide in extramedullary AT, metabolically adapt to this local environment by shifting their metabolism toward fatty acid uptake and oxidation and thereby escape chemotherapy. Targeting fatty acid metabolism not only on the leukemia side but also in the niche might therefore provide an interesting strategy to eradicate LSCs.
Protection of leukemic cells from chemotherapy-induced cytotoxicity by adipocytes?
Evidence is accumulating that leukemic cells, when in close proximity to adipocytes, are protected from chemotherapy-induced cytotoxicity. Mechanisms by which adipocytes might provide shelter to leukemic blasts were intensively studied by Mittelman et al. in both, in vitro and in vivo models [68,69,70,71,72,73]. Murine 8093 pre-B-ALL cells were transplanted into male C57BL/6 mice, which were either obese due to a high fat diet (HFD) or had been fed a normal diet . Obesity did not influence the time of onset of progressive leukemia but it impaired the treatment effect of vincristine  supported by earlier studies showing that vincristine pharmacokinetics can be influenced by HFD-induced obesity in C57BL/6 mice . In this study, the applied vincristine dose was adjusted to total body weight. The obese animals received ~28% more vincristine in total and had comparable levels of the drug in both, circulation and tissues. Thus, the authors concluded that the impaired antileukemic effect was not due to altered vincristine exposure . Most interestingly, numerous leukemia cells were detected in WAT  in different locations  in the mouse models, possibly attracted by SDF1a  suggesting that leukemia cells might hide from chemotherapy in the fat pads. In line, co-culture with adipocytes not only deteriorated the cytotoxic effect of vincristine but also of dexamethasone, daunorubicin, or nilotinib in murine and also human ALL cell lines (SD-1, RS4; 11 and BV173) . Mechanistically, this observation was attributed to an upregulation of the antiapoptotic proteins, B-cell lymphoma 2 and serine/threonine-protein kinase pim-2 by adipocyte co-culture in leukemia cells .
The same syngeneic HFD-ALL mouse model was used for the analysis of the response to l-asparaginase (ASNase) , a first-line drug for ALL treatment which degrades asparagine and glutamine, amino acids essential for the survival of leukemic cells. Adipocytes are an important source of systemic glutamine  and it is well conceivable that high local levels of this amino acid protect from ASNase-induced toxicity. Indeed, comparable to the above described study , obesity significantly reduced survival in response to treatment with ASNase-treated mice compared with lean animals . Via secretion of glutamine adipocytes also reduced the antileukemic effect of ASNase in vitro. This is in line with the finding that expression of glutamine synthetase was increased in BM sections of adolescent patients with leukemia upon induction therapy, yet the plasma levels of asparagine and glutamine are comparable between lean and obese children undergoing high-risk ALL treatment .
Most importantly, WAT is not only able to attract leukemia cells via the secretion of chemotactic factors  but seems to take up and metabolize chemotherapeutic drugs. Adipocytes are characterized by high expression of enzymes capable to convert Daunorubicin to the less effective Daunorubicinol, i.e., aldo–keto reductases (AKR) and carbonyl reductases . AKR activity was detectable in AT explants and 3T3-L1-derived adipocytes. In the presence of adipocytes, there is significantly less accumulation of Daunorubicin in ALL cells as adipocytes can absorb and metabolize anthracyclines . In addition to altering pharmacodynamics, adipocytes might also give protection to leukemia cells by modulating the oxidative stress response . Cell–cell contact with ALL cells or incubation with ALL-conditioned media causes oxidative stress in adipocytes which in turn leads to secretion of yet unknown factors, which mediate protection from Daunorubicin-induced cell death . A summary of the known aspects on how adipocytes influence response of leukemia cells to chemotherapy is illustrated in Fig. 3.
Disrupting adipocyte–leukemic cell interaction as novel therapeutic target
The concept of targeting the interaction of leukemia cells with their specific niche in the BM has emerged only recently [38, 75] and adipocytes should definitively be added to the list of potential target structures. Adipocytes are highly active secretory cells and release a large variety of factors to the local environment and the circulation  (Fig. 4). These comprise proteins, among them classical hormones such as leptin or adiponectin, growth factors, e.g., insulin-like growth factor-1 (IGF-1), vascular endothelial growth factor (VEGF), transforming growth factor-beta (TGFβ), cytokines and chemokines, e.g., interleukin-6 (IL-6), interleukin-8 (IL-8), CC-chemokine ligand 2 (CCL-2), CC-chemokine ligand 20 (CCL-20), SDF-1, components of the extracellular matrix, e.g., fibronectin or collagens, but also binding proteins or enzymes important for the uptake of fatty acids, e.g., FABP4 or lipoprotein lipase. They also include different types of metabolites such as fatty acids, lactate or nucleosides and nucleotides. Especially extracellular ATP (eATP) seems to be of interest in the context of normal and malignant hematopoiesis as eATP has been implicated in mobilization of HSCs from BM to peripheral blood [77, 78] but also interfered with proliferation and homing of AML blasts . Adipocytes also release lipid mediators, e.g., ceramides or eicosanoids such as prostaglandins and leukotrienes, but also bioactive phospholipids. The latter include sphingosine-1-phosphate (S1P) and ceramide-1-phosphate (C1P), which have been identified as potent chemoattractants for HSCs [80, 81] and leukemic cells . Thus, S1P and C1P might also play an important role in migration and homing of leukemic cells into AT. In addition, microRNAs and long noncoding RNAs or extracellular vesicles are also factors secreted by adipocytes . All these different classes of factors might be present in the local microenvironment and influence leukemia cells directly via cell–cell contact or in a paracrine manner, but also via impacting other cell types present in the BMM. Mechanisms of action include stimulation of proliferation and survival of leukemia cells, maintaining leukemia cells in the niche by an inviting matrix and/or a chemotactic gradient, modulation of the vascular niche/angiogenesis in the BM, protection from chemotherapy and well conceivably, delivery of nutrients, and alteration of leukemia cell gene expression or metabolism (Fig. 4). Aging leads to a massive increase in MAT and age is a major risk factor for leukemia. Whether adipocytes, similar to osteoprogenitors , can contribute to the development and onset of leukemia in the BMM is unclear at this point.
Recent scRNA-seq studies on murine BM stroma identified factors with specific relevance for leukemia treatment. For example, the compartment of leptin receptor-positive (Lepr+) cells was analyzed, which contained four different clusters of which two expressed adipogenesis-associated marker genes . Interestingly, these two adipocytic-primed clusters of Lepr+ cells were identified as major source of prohematopoietic factors in the BMM, amongst them SDF-1 (Cxcl12), SCF (Kitl), IL-7 (Il7), IL-15 (Il15), IL-34 (Il-34), M-CSF (Csf1), BMP-4 (Bmp4), CCL-19 (Ccl19), and CCL-2 (Ccl-2) . Gene expression analyses on human samples confirmed an enrichment of inflammatory genes in BM adipocytes . Several of these factors are already exploited for the treatment of solid tumors and/or leukemia or are in preclinical testing and clinical trials (for review see ). Whether the mode of action of novel compounds, e.g., neutralizing antibodies involves adipocytes or other cell types as source of inflammatory factors in the local niche is not clear at this point. Also, whether modulating the adipocyte compartment in the BM may serve as a sensitizing strategy requires further study. Based on the major part of the recent literature adipocytes provide a protective environment, acting as “friends” of leukemia cells. Thus, eliminating adipocytes from the BMM might help to eliminate leukemic cells. However, getting rid of BM adipocytes is a complicated task as there is only a very limited number of factors reducing MAT including parathyroid hormone , the diabetes medication metformin , mechanical loading , and exercise . One study by Liu et al. reports that chemotherapy leads to an inhibition of adipogenesis in the BM via mononuclear cell-derived growth differentiation factor 15 (GDF-15), in turn reinforcing the efficacy of consolidation chemotherapy in AML patients during complete remission .
Fasting, a condition known to enhance MAT, inhibited the engraftment and progression of B-ALL and T-ALL in several mouse model systems tested . From this finding, one might conclude that adipocytes are “enemies” of leukemia cells in the BMM. Lu et al. did not comment on BM adipocytes in their study but they report that, as expected, fasting induced a drop in circulating and local leptin levels . Leptin is known to inhibit adipogenesis in the BM in vitro and in vivo [90, 91], thus we can expect an increase in MAT with low levels of leptin. Most likely due to low leptin, they identified an upregulation of Lepr expression in leukemia cells and activation of downstream signaling routes as main cause leading to inhibition of leukemia initiation and progression. Vice versa, attenuated Lepr expression was identified as essential for development and maintenance of ALL . All in all, the leptin/Lepr axis is an interesting new target for leukemia treatment.
Besides acting as a member of the local BMM, adipocytes can certainly also interact with leukemia cells via their secreted factors in an endocrine manner. This assumption is underlined by the fact that obesity, which is characterized by the excessive accumulation of WAT, leads to an increased risk of developing and dying from leukemia as recently revealed in a meta-analysis of prospective cohort studies . The fact that leukemia cells use WAT as a hideaway to escape chemotherapy should also be taken into account. Therefore, not only strategies to reduce MAT but also WAT might be useful to support leukemia treatment and also maintain remission.
Open questions and future directions of scientific research
Fasting is currently propagated as the holy grail of cancer treatment by some researchers . Since a complete abstinence from all food and drinks except water is hard to achieve, specific fasting-mimicking diets (FMDs) were developed. These diets are designed to mimic the beneficial effects of fasting. They include proteins and carbohydrates and make up a daily energy intake of 300–1000 kcal. They have reduced nutritional risk compared with complete abstinence and a much better patient compliance (for review see ). The dietary regime is applied in cycles, e.g., 1–5 days of fasting every 3–4 weeks . Intensive research is urgently needed in this area to determine long-term outcome and sequelae of such interventions [94, 95]. The first results seem very promising as fasting or FMDs show robust anticancer effects in animal models and also in clinical trials , yet the effect on hematological disease is largely unexplored. Fasting interventions have an impact on systemic metabolism, basically switching the body into a mode of making use of its energy stores, which are mainly represented by WAT. The hallmark of the fasting response includes low levels of glucose and insulin, high levels of glucagon and ketone bodies, low levels of leptin and IGF-1 and high levels of adiponectin (for review see ). In normal cells, the altered circulating levels of metabolites and hormones will lead to a shutdown of metabolic activity and cell cycling, resulting in a protection from chemotherapeutic insults. In contrast, malignant cells can show the opposite response and are therefore sensitized to chemotherapy and also other therapeutic options.
It is very obvious that the key alterations induced by fasting are related to altered function of AT. A decrease in leptin and a subsequent upregulation of Lepr was already identified as protective mechanism in B-ALL and T-ALL development . It will be important to identify other adipocyte-secreted factors that contribute to the beneficial effects of fasting in cancer therapy in general and in leukemia in particular. Leukemia develops in the BM. Thus, the effect of fasting on BM adipocytes needs to be dissected in detail. For example, a recent paper by Attané et al. described that BM adipocytes display distinct metabolic characteristics with an absence of lipolytic activity and a shift toward a cholesterol-oriented metabolism . How this impacts on the interaction between BM adipocytes and leukemia needs to be investigated. It is also important to find out why fasting seems to be beneficial in ALL, but not AML. This might be related to different metabolic demands and signaling capacities of lymphoid and myeloid cells. Most importantly, we should aim at investigating whether fasting itself is required or if the fasting procedure can be mimicked by pharmacological agents, the polyphenolic compound resveratrol (RSV) being a prominent example . RSV inhibits adipogenic differentiation and the expression of proinflammatory factors from adipocytes . At the same time, RSV sensitizes leukemia cells to apoptosis induction . It is conceivable that RSV also influences the interaction of both cell types in the local niche. Metformin is another promising candidate in this regard—it molecularly mimics caloric restriction , reduces the cancer incidence in both mice and humans  and, of note, reduces MAT . By the way, comparable considerations may also apply to exercise. Physical exercise is beneficial during and after cancer treatment  and leads to the loss of WAT mass  and, importantly, also MAT .
Another important finding that requires appropriate follow-up is the accumulation of leukemia cells in WAT found in several mouse models [67, 68, 71] but also in humans . In this old study dating back to 1962, WAT samples of 60 patients who died of leukemia or lymphoma were analyzed. 19 of them showed subcutaneous WAT infiltrations of malignant cells in apparently normal skin . This is a remarkable observation, given the fact that WAT was commonly regarded as negligible organ in leukemia. WAT seems to serve as a hideaway for leukemic cells and supports evasion from chemotherapy as adipocytes are able to provide a protective environment, in part by metabolizing chemotherapeutic drugs [67,68,69,70,71,72,73]. Therefore, the accumulation of WAT in obesity hampers chemotherapy [68, 69, 73]. In animal studies, the dosage of chemotherapeutics used was adjusted to body weight. Of note, although obese animals received ~28% more vincristine, they had comparable levels in the circulation and in tissues . The question arising from this observation is whether patients with an increased fat mass are actually underdosed. The body surface area is commonly used to calculate dosages for chemotherapeutic drugs and the commonly used formulas fit fairly well also in overweight and obese patients . Nevertheless, altered pharmacodynamics in WAT should be taken into account, also in postremission therapy. This is underlined by the fact that obesity is associated with poorer outcome in several types of leukemia, including acute promyelocytic leukemia, AML, and pediatric pre-B-ALL [104,105,106].
Taken together, although neglected in the past, MAT as well as WAT should be considered important and relevant in the context of leukemia. Their secretion products such as growth factors, cytokines, chemokines, matrix molecules, or metabolites have an impact on the function of leukemic cells opening up new therapeutic opportunities to fight hematological malignancy.
Walter MJ, Shen D, Ding L, Shao J, Koboldt DC, Chen K, et al. Clonal architecture of secondary acute myeloid leukemia. N Engl J Med. 2012;366:1090–8.
Shlush LI, Zandi S, Mitchell A, Chen WC, Brandwein JM, Gupta V, et al. Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia. Nature. 2014;506:328–33.
Mullighan CG. The genomic landscape of acute lymphoblastic leukemia in children and young adults. Hematology. 2014;2014:174–80.
MHGP Raaijmakers, Mukherjee S, Guo S, Zhang S, Kobayashi T, Schoonmaker JA, et al. Bone progenitor dysfunction induces myelodysplasia and secondary leukaemia. Nature. 2010;464:852–7.
Burger JA, Peled A. CXCR4 antagonists: targeting the microenvironment in leukemia and other cancers. Leukemia. 2009;23:43–52.
Cho BS, Kim HJ, Konopleva M. Targeting the CXCL12/CXCR4 axis in acute myeloid leukemia: from bench to bedside. Korean J Intern Med. 2017;32:248–57.
Lengyel E, Makowski L, DiGiovanni J, Kolonin MG. Cancer as a matter of fat: the crosstalk between adipose tissue and tumors. Trends Cancer. 2018;4:374–84.
Rosen ED, Spiegelman BM. What we talk about when we talk about fat. Cell.2014;156:20–44.
Bartelt A, Heeren J. Adipose tissue browning and metabolic health. Nat Rev Endocrinol. 2014;10:24–36.
Chouchani ET, Kazak L, Spiegelman BM. New advances in adaptive thermogenesis: UCP1 and beyond. Cell Metab. 2019;29:27–37.
Kajimura S, Spiegelman BM, Seale P. Brown and beige fat: physiological roles beyond heat generation. Cell Metab. 2015;22:546–59.
Giordano A, Smorlesi A, Frontini A, Barbatelli G, Cinti S. Mechanisms in endocrinology: white, brown and pink adipocytes: the extraordinary plasticity of the adipose organ. Eur J Endocrinol. 2014;170:R159–71.
Cawthorn WP, Scheller EL, Learman BS, Parlee SD, Simon BR, Mori H, et al. Bone marrow adipose tissue is an endocrine organ that contributes to increased circulating adiponectin during caloric restriction. Cell Metab. 2014;20:368–75.
Liu LF, Shen WJ, Ueno M, Patel S, Kraemer FB. Characterization of age-related gene expression profiling in bone marrow and epididymal adipocytes. BMC Genom. 2011;12. https://doi.org/10.1186/1471-2164-12-212.
Attané C, Estève D, Chaoui K, Iacovoni JS, Corre J, Moutahir M, et al. Human bone marrow is comprised of adipocytes with specific lipid metabolism. Cell Rep. 2020;30:949–58.e6.
Seita J, Weissman IL. Hematopoietic stem cell: self-renewal versus differentiation. Wiley Interdiscip Rev Syst Biol Med. 2010;2:640–53.
Chen Q, Shou P, Zheng C, Jiang M, Cao G, Yang Q, et al. Fate decision of mesenchymal stem cells: adipocytes or osteoblasts? Cell Death Differ. 2016;23:1128–39.
Xu R, Taskin MB, Rubert M, Seliktar D, Besenbacher F, Chen M. HiPS-MSCs differentiation towards fibroblasts on a 3D ECM mimicking scaffold. Sci Rep. 2015;5:1–7.
Agarwala S, Tamplin OJ. Neural crossroads in the hematopoietic stem cell niche. Trends Cell Biol. 2018;28:987–98.
Crisan M. Transition of mesenchymal stem/stromal cells to endothelial cells. Stem Cell Res Ther. 2013;4:2–4.
Tikhonova AN, Dolgalev I, Hu H, Sivaraj KK, Hoxha E, Cuesta-Domínguez Á, et al. The bone marrow microenvironment at single-cell resolution. Nature. 2019;569:222–8.
Baryawno N, Przybylski D, Kowalczyk MS, Kfoury Y, Severe N, Gustafsson K, et al. A cellular taxonomy of the bone marrow stroma in homeostasis and leukemia. Cell. 2019;177:1915–32.e16.
Asada N, Kunisaki Y, Pierce H, Wang Z, Fernandez NF, Birbrair A, et al. Differential cytokine contributions of perivascular haematopoietic stem cell niches. Nat Cell Biol. 2017;19:214–23.
Ding L, Morrison SJ. Haematopoietic stem cells and early lymphoid progenitors occupy distinct bone marrow niches. Nature. 2013;495:231–5.
Greenbaum A, Hsu YMS, Day RB, Schuettpelz LG, Christopher MJ, Borgerding JN, et al. CXCL12 in early mesenchymal progenitors is required for haematopoietic stem-cell maintenance. Nature. 2013;495:227–30.
Sugiyama T, Kohara H, Noda M, Nagasawa T. Maintenance of the hematopoietic stem cell pool by CXCL12-CXCR4 chemokine signaling in bone marrow stromal cell niches. Immunity. 2006;25:977–88.
Zhou BO, Yu H, Yue R, Zhao Z, Rios JJ, Naveiras O, et al. Bone marrow adipocytes promote the regeneration of stem cells and haematopoiesis by secreting SCF. Nat Cell Biol. 2017;19:891–903.
Zhang Z, Huang Z, Ong B, Sahu C, Zeng H, Bin. RuanH. Bone marrow adipose tissue-derived stem cell factor mediates metabolic regulation of hematopoiesis. Haematologica. 2019;104:1731–43.
Schofield R. The relationship between the spleen colony-forming cell and the haemopoietic stem cell. Blood Cells. 1978;4:7–25.
Acar M, Kocherlakota KS, Murphy MM, Peyer JG, Oguro H, Inra CN, et al. Deep imaging of bone marrow shows non-dividing stem cells are mainly perisinusoidal. Nature. 2015;526:126–30.
Kiel MJ, Yilmaz ÖH, Iwashita T, Yilmaz OH, Terhorst C, Morrison SJ. SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells. Cell. 2005;121:1109–21.
Kiel MJ, Radice GL, Morrison SJ. Lack of evidence that hematopoietic stem cells depend on N-cadherin-mediated adhesion to osteoblasts for their maintenance. Cell Stem Cell. 2007;1:204–17.
Calvi LM, Adams GB, Weibrecht KW, Weber JM, Olson DP, Knight MC, et al. Osteoblastic cells regulate the haematopoietic stem cell niche. Nature. 2003;425:841–6.
Zhang J, Niu C, Ye L, Huang H, He X, Tong WG, et al. Identification of the haematopoietic stem cell niche and control of the niche size. Nature. 2003;425:836–41.
Morrison SJ, Scadden DT. The bone marrow niche for haematopoietic stem cells. Nature. 2014;505:327–34.
Bukowska J, Frazier T, Smith S, Brown T, Bender R, McCarthy M, et al. Bone marrow adipocyte developmental origin and biology. Curr Osteoporos Rep. 2018;16:312–9.
Veldhuis-Vlug AG, Rosen CJ. Clinical implications of bone marrow adiposity. 2018. https://doi.org/10.1111/joim.12718.
Reagan MR, Rosen CJ. Navigating the bone marrow niche: translational insights and cancer-driven dysfunction. Nat Rev Rheumatol. 2016;12:154–68.
Robles H, Park SJ, Joens MS, Fitzpatrick JAJ, Craft CS, Scheller EL. Characterization of the bone marrow adipocyte niche with three-dimensional electron microscopy. Bone. 2019;118:89–98.
MT Marrow adipose cells. Histochemical identification of labile and stable components. Arch Pathol Lab Med. 1976;100:16–8.
Scheller EL, Doucette CR, Learman BS, Cawthorn WP, Khandaker S, Schell B, et al. Region-specific variation in the properties of skeletal adipocytes reveals regulated and constitutive marrow adipose tissues. Nat Commun. 2015;6:7808.
Laharrague P, Larrouy D, Fontanilles A, Truel N, Campfield A, Tenenbaum R, et al. High expression of leptin by human bone marrow adipocytes in primary culture. FASEB J. 1998;12:747–52.
Margetic S, Gazzola C, Pegg G, Hill R. Leptin: a review of its peripheral actions and interactions. Int J Obes. 2002;26:1407–33.
Justesen J, Stenderup K, Ebbesen EN, Mosekilde L, Steiniche T, Kassem M. Adipocyte tissue volume in bone marrow is increased with aging and in patients with osteoporosis. Biogerontology. 2001;2:165–71.
Yeung DKW, Griffith JF, Antonio GE, Lee FKH, Woo J, Leung PC. Osteoporosis is associated with increased marrow fat content and decreased marrow fat unsaturation: a proton MR spectroscopy study. J Magn Reson Imaging. 2005;22:279–85.
Bredella MA, Torriani M, Ghomi RH, Thomas BJ, Brick DJ, Gerweck AV, et al. Vertebral bone marrow fat is positively associated with visceral fat and inversely associated with IGF-1 in obese women. Obesity. 2011;19:49–53.
Napoli N, Chandran M, Pierroz DD, Abrahamsen B, Schwartz AV, Ferrari SL. Mechanisms of diabetes mellitus-induced bone fragility. Nat Rev Endocrinol. 2017;13:208–19.
Bredella MA, Fazeli PK, Miller KK, Misra M, Torriani M, Thomas BJ, et al. Increased bone marrow fat in anorexia nervosa. J Clin Endocrinol Metab. 2009;94:2129–36.
Cawthorn WP, Scheller EL, Parlee SD, Pham HA, Learman BS, Redshaw CMH, et al. Expansion of bone marrow adipose tissue during caloric restriction is associated with increased circulating glucocorticoids and not with hypoleptinemia. Endocrinology. 2016;157:508–21.
Styner M, Pagnotti GM, McGrath C, Wu X, Sen B, Uzer G, et al. Exercise decreases marrow adipose tissue through ss-oxidation in obese running mice. J Bone Miner Res. 2017;32:1692–702.
Mostoufi-Moab S, Magland J, Isaacoff EJ, Sun W, Rajapakse CS, Zemel B, et al. Adverse fat depots and marrow adiposity are associated with skeletal deficits and insulin resistance in long-term survivors of pediatric hematopoietic stem cell transplantation. J Bone Miner Res. 2015;30:1657–66.
Nguyen TV, Melville A, Nath S, Story C, Howell S, Sutton R, et al. Bone marrow recovery by morphometry during induction chemotherapy for acute lymphoblastic leukemia in children. PLoS One. 2015;10:1–10.
Vande Berg BC, Malghem J, Lecouvet FE, Devogelaer JP, Maldague B, Houssiau FA. Fat conversion of femoral marrow in glucocorticoid-treated patients: a cross-sectional and longitudinal study with magnetic resonance imaging. Arthritis Rheum. 1999;42:1405–11.
Ghali O, Al Rassy N, Hardouin P, Chauveau C. Increased bone marrow adiposity in a context of energy deficit: the tip of the iceberg? Front Endocrinol. 2016;7:1–7.
Naveiras O, Nardi V, Wenzel PL, Hauschka PV, Fahey F, Daley GQ. Bone-marrow adipocytes as negative regulators of the haematopoietic microenvironment. Nature. 2009;460:259–63.
Zhu RJ, Wu MQ, Li ZJ, Zhang Y, Liu KY. Hematopoietic recovery following chemotherapy is improved by BADGE-induced inhibition of adipogenesis. Int J Hematol. 2013;97:58–72.
Ambrosi TH, Scialdone A, Graja A, Gohlke S, Jank AM, Bocian C, et al. Adipocyte accumulation in the bone marrow during obesity and aging impairs stem cell-based hematopoietic and bone regeneration. Cell Stem Cell. 2017;20:771–84.e6.
Wilson A, Fu H, Schiffrin M, Winkler C, Koufany M, Jouzeau JY, et al. Lack of adipocytes alters hematopoiesis in lipodystrophic mice. Front Immunol. 2018;9. https://doi.org/10.3389/fimmu.2018.02573.
Boyd AL, Reid JC, Salci KR, Aslostovar L, Benoit YD, Shapovalova Z, et al. Acute myeloid leukaemia disrupts endogenous myelo-erythropoiesis by compromising the adipocyte bone marrow niche. Nat Cell Biol. 2017;19:1336–47.
Cahu X, Calvo J, Poglio S, Prade N, Colsch B, Arcangeli M-L, et al. Bone marrow sites differently imprint dormancy and chemoresistance to T-cell acute lymphoblastic leukemia. Blood Adv. 2017;1:1760–72.
Shafat MS, Oellerich T, Mohr S, Robinson SD, Edwards DR, Marlein CR, et al. Leukemic blasts program bone marrow adipocytes to generate a protumoral microenvironment. Blood. 2017;129:1320–32.
Lu Z, Xie J, Wu G, Shen J, Collins R, Chen W, et al. Fasting selectively blocks development of acute lymphoblastic leukemia via leptin-receptor upregulation. Nat Med. 2017;23:79–90.
Nowak D, Stewart D, Koeffler HP. Differentiation therapy of leukemia: 3 decades of development. Blood. 2009;113:3655–65.
Cheng CW, Yilmaz ÖH. Starving leukemia to induce differentiation. Nat Med. 2017;23:14–15.
Trubowitz S, Sims CF. Subcutaneous fat in leukemia and lymphoma. Arch Dermatol. 1962;86:520–4.
Han J, Koh YJ, Moon HR, Ryoo HG, Cho CH, Kim I, et al. Adipose tissue is an extramedullary reservoir for functional hematopoietic stem and progenitor cells. Blood. 2010;115:957–64.
Ye H, Adane B, Khan N, Sullivan T, Minhajuddin M, Gasparetto M, et al. Leukemic stem cells evade chemotherapy by metabolic adaptation to an adipose tissue niche. Cell Stem Cell. 2016;19:23–37.
Behan JW, Yun JP, Proektor MP, Ehsanipour EA, Arutyunyan A, Moses AS, et al. Adipocytes impair leukemia treatment in mice. Cancer Res. 2009;69:7867–74.
Behan JW, Avramis VI, Yun JP, Louie SG, Mittelman SD. Diet-induced obesity alters vincristine pharmacokinetics in blood and tissues of mice. Pharm Res. 2010;61:385–90.
Ehsanipour EA, Sheng X, Behan JW, Wang X, Butturini A, Avramis VI, et al. Adipocytes cause leukemia cell resistance to l-asparaginase via release of glutamine. Cancer Res. 2013;73:2998–3006.
Pramanik R, Sheng X, Ichihara B, Heisterkamp N, Mittelman SD. Adipose tissue attracts and protects acute lymphoblastic leukemia cells from chemotherapy. Leuk Res. 2013;37:503–9.
Sheng X, Tucci J, Parmentier JH, Ji L, Behan JW, Heisterkamp N, et al. Adipocytes cause leukemia cell resistance to daunorubicin via oxidative stress response. Oncotarget. 2016;7:73147–59.
Sheng X, Parmentier J-H, Tucci J, Pei H, Cortez-Toledo O, Dieli-Conwright CM, et al. Adipocytes sequester and metabolize the chemotherapeutic daunorubicin. Mol Cancer Res. 2017;15:1704–13.
Frayn KN, Khan K, Coppack SW, Elia M. Amino acid metabolism in human subcutaneous adipose tissue in vivo. Clin Sci. 1991;80:471–4.
Schepers K, Campbell TB, Passegué E. Normal and leukemic stem cell niches: insights and therapeutic opportunities. Cell Stem Cell. 2015;16:254–67.
Funcke J-B, Scherer PE. Beyond adiponectin and leptin: adipose tissue-derived mediators of inter-organ communication. J Lipid Res. 2019;60:1648–84.
Adamiak M, Bujko K, Cymer M, Plonka M, Glaser T, Kucia M, et al. Novel evidence that extracellular nucleotides and purinergic signaling induce innate immunity-mediated mobilization of hematopoietic stem/progenitor cells. Leukemia. 2018;32:1920–31.
Ratajczak MZ, Adamiak M, Thapa A, Bujko K, Brzezniakiewicz-Janus K, Lenkiewicz AM. NLRP3 inflammasome couples purinergic signaling with activation of the complement cascade for the optimal release of cells from bone marrow. Leukemia. 2019;33:815–25.
Salvestrini V, Zini R, Rossi L, Gulinelli S, Manfredini R, Bianchi E, et al. Purinergic signaling inhibits human acute myeloblastic leukemia cell proliferation, migration, and engraftment in immunodeficient mice. Blood. 2012;119:217–26.
Kim CH, Wu W, Wysoczynski M, Abdel-latif A, Sunkara M. Conditioning for hematopoietic transplantation proteolytic environment in bone marrow—a novel role for bioactive lipids and soluble C5b-C9 as homing factors. Leukemia. 2012;26:106–16.
Ratajczak MZ, Lee H, Wysocyzynski M, Wan W, Marlicz W, Laughlin MJ, et al. Plasma sphingosine 1-phosphate is a major chemoattractant that directs egress of hematopoietic stem progenitor cells from the bone marrow and its level in peripheral blood increases during mobilization due to activation of complement cascade/membrane attack complex. Leukemia. 2010;24:976–85.
Abdelbaset-Ismail A, Cymer M, Borkowska-Rzeszotek S, Brzeźniakiewicz-Janus K, Rameshwar P, Kakar SS, et al. Bioactive phospholipids enhance migration and adhesion of human leukemic cells by inhibiting heme oxygenase 1 (HO-1) and inducible nitric oxygenase synthase (iNOS) in a p38 MAPK-dependent manner. Stem Cell Rev Rep. 2019;15:139–54.
Miggitsch C, Meryk A, Naismith E, Pangrazzi L, Ejaz A, Jenewein B, et al. Human bone marrow adipocytes display distinct immune regulatory properties. EBioMedicine. 2019;46:387–98.
Jöhrer K, Ploner C, Thangavadivel S, Wuggenig P, Greil R. Adipocyte-derived players in hematologic tumors: useful novel targets? Expert Opin Biol Ther. 2015;15:61–77.
Fate MC, Fan Y, Hanai J, Le PT, Dempster DW, Rosen CJ, et al. Article parathyroid hormone directs. Cell Metab. 2017;25:661–72.
Bornstein S, Moschetta M, Kawano Y, Sacco A, Huynh D, Brooks D, et al. Metformin affects cortical bone mass and marrow adiposity in diet-induced obesity in male mice. Endocrinology. 2017;158:3369–85.
David V, Martin A, Lafage-Proust MH, Malaval L, Peyroche S, Jones DB, et al. Mechanical loading down-regulates peroxisome proliferator-activated receptor γ in bone marrow stromal cells and favors osteoblastogenesis at the expense of adipogenesis. Endocrinology. 2007;148:2553–62.
Pagnotti GM, Styner M. Exercise regulation of marrow adipose tissue. Front Endocrinol. 2016;7:1–10.
Liu H, Zhai Y, Zhao W, Wan Y, Lu W, Yang S, et al. Consolidation chemotherapy prevents relapse by indirectly regulating bone marrow adipogenesis in patients with acute myeloid leukemia. Cell Physiol Biochem. 2018;45:2389–2400.
Thomas T, Gori F, Khosla S, Jensen MD, Burguera B, Riggs BL. Leptin acts on human marrow stromal cells to enhance differentiation to osteoblasts and to inhibit differentiation to adipocytes. Endocrinology. 1999;140:1630–8.
Devlin MJ, Brooks DJ, Conlon C, van Vliet M, Louis L, Rosen CJ, et al. Daily leptin blunts marrow fat but does not impact bone mass in calorie-restricted mice. J Endocrinol. 2016;229:295–306.
Castillo JJ, Reagan JL, Ingham RR, Furman M, Dalia S, Merhi B, et al. Obesity but not overweight increases the incidence and mortality of leukemia in adults: a meta-analysis of prospective cohort studies. Leuk Res. 2012;36:868–75.
Nencioni A, Caffa I, Cortellino S, Longo VD. Fasting and cancer: molecular mechanisms and clinical application. Nat Rev Cancer. 2018;18:707–19.
Caccialanza R, Cereda E, De Lorenzo F, Farina G, Pedrazzoli P. To fast, or not to fast before chemotherapy, that is the question. BMC Cancer. 2018;18:10–13.
Caccialanza R, Aprile G, Cereda E, Pedrazzoli P. Fasting in oncology: a word of caution. Nat Rev Cancer. 2019;19:177.
Lee SH, Min KJ. Caloric restriction and its mimetics. BMB Rep. 2013;46:181–7.
Fischer-Posovszky P, Kukulus V, Tews D, Unterkircher T, Debatin K-M, Fulda S, et al. Resveratrol regulates human adipocyte number and function in a Sirt1-dependent manner. Am J Clin Nutr. 2010;92. https://doi.org/10.3945/ajcn.2009.28435.
Frazzi R, Guardi M. Cellular and molecular targets of resveratrol on lymphoma and leukemia cells. Molecules. 2017;22:1–15.
Dhahbi JM, Mote PL, Fahy GM, Spindler SR. Identification of potential caloric restriction mimetics by microarray profiling. Physiol Genom. 2005;23:343–50.
Yu H, Zhong X, Gao P, Shi J, Wu Z, Guo Z, et al. The potential effect of metformin on cancer: an umbrella review. Front Endocrinol. 2019;10. https://doi.org/10.3389/fendo.2019.00617.
Galvão DA, Newton RU. Review of exercise intervention studies in cancer patients. J Clin Oncol. 2005;23:899–909.
Thompson D, Karpe F, Lafontan M, Frayn K. Physical activity and exercise in the regulation of human adipose tissue physiology. Physiol Rev. 2012;92:157–91.
Verbraecken J, Van De Heyning P, De Backer W, Van Gaal L. Body surface area in normal-weight, overweight, and obese adults. A comparison study. Metabolism. 2006;55:515–24.
Li S, Chen L, Jin W, Ma X, Ma Y, Dong F, et al. Influence of body mass index on incidence and prognosis of acute myeloid leukemia and acute promyelocytic leukemia: a meta-analysis. Sci Rep. 2017;7:1–10.
Dhakal P, Lyden E, Lee A, Michalski J, Al-Kadhimi ZS, Maness LJ. et al. Effects of obesity on overall survival of adults with acute myeloid leukemia. Clin Lymphoma Myeloma Leuk. 2020;20:e131–6.
Orgel E, Tucci J, Alhushki W, Malvar J, Sposto R, Fu CH, et al. Obesity is associated with residual leukemia following induction therapy for childhood B-precursor acute lymphoblastic leukemia. Blood. 2014;124:3932–8.
This project received funding from the Collaborative Research Centre 1074 (Experimental Models and Clinical Translation in Leukemia), German Research Foundation. JZ is funded by a Margarete von Wrangell scholarship (Baden-Wuerttemberg Ministry of Science, Research, and Arts) and received funding from the Hertha Nathorff program (Medical Faculty, Ulm University). PF-P holds a Heisenberg professorship (FI 1700/7–1) of the German Research Foundation.
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The authors declare that they have no conflict of interest.
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Zinngrebe, J., Debatin, KM. & Fischer-Posovszky, P. Adipocytes in hematopoiesis and acute leukemia: friends, enemies, or innocent bystanders?. Leukemia 34, 2305–2316 (2020). https://doi.org/10.1038/s41375-020-0886-x
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