Abstract
Background
Neuroendocrine phenotype is commonly associated with therapy resistance and poor prognoses in small-cell neuroendocrine cancers (SCNCs), such as neuroendocrine prostate cancer (NEPC) and small-cell lung cancer (SCLC). Expression levels of current neuroendocrine markers exhibit high case-by-case variability, so multiple markers are used in combination to identify SCNCs. Here, we report that ACAA2 is elevated in SCNCs and is a potential molecular indicator for SCNCs.
Methods
ACAA2 expressions in tumour xenografts, tissue microarrays (TMAs), and patient tissues from prostate and lung cancers were analysed via immunohistochemistry. ACAA2 mRNA levels in lung and prostate cancer (PC) patients were assessed in published datasets.
Results
ACAA2 protein and mRNA levels were elevated in SCNCs relative to non-SCNCs. Medium/high ACAA2 intensity was observed in 78% of NEPC PDXs samples (N = 27) relative to 33% of adeno-CRPC (N = 86), 2% of localised PC (N = 50), and 0% of benign prostate specimens (N = 101). ACAA2 was also elevated in lung cancer patient tissues with neuroendocrine phenotype. 83% of lung carcinoid tissues (N = 12) and 90% of SCLC tissues (N = 10) exhibited medium/high intensity relative to 40% of lung adenocarcinoma (N = 15).
Conclusion
ACAA2 expression is elevated in aggressive SCNCs such as NEPC and SCLC, suggesting it is a potential molecular indicator for SCNCs.
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Introduction
Neuroendocrine (NE) phenotype in lung and prostate cancer frequently correlates with an aggressive clinical course, therapy resistance, and widespread metastasis, which contributes to worse clinical outcomes [1, 2]. For instance, neuroendocrine prostate cancer (NEPC) is the most lethal subtype of prostate cancer, and small-cell lung cancer (SCLC) is also an aggressive, highly lethal subtype of lung cancer [3]. Studies have demonstrated that these small-cell neuroendocrine cancers (SCNCs) from different tissues are more similar to each other than to adenocarcinomas from the same tissue site despite differences in the tissue of origin [4]. They share many histopathological commonalities in morphology, such as high nuclear-to-cytoplasm ratios, poorly defined borders, and granular chromatin [1, 5]. SCNCs also share common gene alterations and an expression of a common set of markers, including synaptophysin (SYP), chromogranin A (CHGA), and CD56, suggesting common drivers and transdifferentiating pathways [1, 5, 6].
The cell of origin of SCNCs remains unclear. Previous studies observed that tumours containing both NE and adenocarcinoma features display an increase of NE phenotype over time during disease progression and the onset of treatment resistance, thereby suggesting that NE transdifferentiation may arise from adenocarcinoma precursors [1, 6, 7]. SCNCs such as NEPC and SCLC can arise from heavily treated adenocarcinoma via cancer’s adaptive response, increased stemness, and lineage plasticity, which enhances therapy resistance [8,9,10]. For instance, once castration-resistant prostate adenocarcinoma (adeno-CRPC) gains NE phenotype and advances to NEPC during intensive treatment with a new generation of anti-androgen therapies, its median survival decreases to about 7 months, and these diseases are resistant to conventional anti-androgen therapies due to loss of dependence on AR signalling pathways [10,11,12,13,14,15,16].
Current clinical identification of SCNCs relies on morphological characteristics and histological markers such as SYP, CHGA, and CD56. However, the expression of these markers varies based on the patient, which limits the reliability of any single histological markers [4, 17]. Thus, multiple markers must be used in combination to effectively assess the presence of NE phenotypes since SCNC tumours can express various profiles of NE markers [4, 17]. In addition, the search for common molecular indicators across SCNCs may potentially lead to the discovery of new NE driver pathways, precision oncology, and new targeted therapies [18].
A common transdifferentiation across SCNCs suggests mutual vulnerabilities and treatment targets, rendering a shared targeted therapy across SCNCs a possibility [6, 19, 20]. We hypothesise that uncovering the common oncogenic pathways in SCNCs fosters the identification of common therapeutic targets across these aggressive tumours [19]. Therapies targeting mutual pathways of SCNCs, such as Myc-targeting Aurora kinase inhibition [21,22,23] and EZH2 inhibition (NCT03460977; NCT03480646), are currently being explored in NEPC, SCLC, and other NE cancers [1, 24, 25].
To identify new molecular indicators and therapeutic targets for SCNCs, we analysed a previously published proteomic dataset containing SCNC and non-SCNC tumours [26]. We demonstrated that Acetyl-CoA acyltransferase 2 (ACAA2) is highly upregulated in a Trop2-driven NEPC (TD-NEPC) model [26]. ACAA2, also known as 3-ketoacyl-CoA thiolase, is a rate-limiting enzyme in the mitochondria that is responsible for catalysing the last step of the mitochondrial beta-oxidation pathway [27,28,29]. ACAA2 is associated with cardiovascular risks and lipid metabolism, but its role in cancer has not been fully elucidated [30,31,32,33]. A previous study suggests that SCNCs are susceptible to disruptions of genes in the lipid metabolism pathway through genome-wide functional RNA interference screens [4]. Here, we report that ACAA2 expression is increased in SCNCs relative to non-SCNCs in cell lines, tumour xenografts, and patient transcriptomic datasets, suggesting ACAA2 as a potential molecular indicator for these malignancies.
Materials and methods
Cell culture
The human prostate cancer cell lines used, including LNCaP, C4-2, 22RV1, DU145, PC3, ARCaP, and NCI-H660 were purchased from the American Type Culture Collection (ATCC). Castration-sensitive prostate cancer (CSPC) cell line, LNCaP, was used to overexpress Trop2 to generate the Trop2-driven NEPC (TD-NEPC) as described in Hsu et al. (2020) [26]. LNCaP, C4-2, 22RV1, DU145, PC3, ARCaP, and TD-NEPC cells were maintained in RPMI 1640 medium (Thermo Fisher Scientific), which was supplemented with 10% FBS, 100 U/ml penicillin, and 100X GlutaMAX. NCI-H660 cells were cultured in RPMI 1640 medium with 5% fetal bovine serum, 0.005 mg/ml insulin, 0.01 mg/ml transferrin, 30 nM sodium selenite, 10 nM hydrocortisone, 10 nM beta-estradiol, 4 mM L-glutamine.
Western blot (WB)
Cells were collected from culture and lysed using RIPA lysis buffer with protease and phosphatase inhibitors (Thermo Fisher Scientific). BCA assay was performed to measure protein concentration of the lysate, and equal amounts of protein (40 μg/20 μl) were added for each sample. SDS buffer was added to samples, and heat denaturation was performed at 95 °C for 5 min. Samples were loaded and separated by 8–16% SDS-PAGE gel (Invitrogen™ XP08165BOX), transferred onto a 0.22 μm nitrocellulose membrane (GVS Life Sciences, 1212632), and blocked for an hour under room temperature with 5% non-fat milk. The blocked membrane was then incubated with primary antibodies overnight at 4 °C. Anti-ACAA2 was purchased from Abcam (ab128929, 1:1000 dilution), and GAPDH (sc-47724, 1:2000 dilution) was used as an internal control. After overnight incubation, blots were washed with TBST 3 times, 5 min each. Then, blots were incubated for an hour in secondary antibodies, purchased from Fisher Scientific, with HRP conjugation (PI31432 and PI31462, 1:5000 dilution). The signal was detected using PierceTM ECL Western Blotting Substrate (Thermo Fisher Scientific).
Xenografts
For all the prostate cancer cell lines, 106 cells were mixed with Matrigel (100 μL) and implanted into the flanks of 6-to-8-weeks old male NSG (NOD-SCID-IL2Rγ-null) mice via subcutaneous injection. Xenografts were then harvested from these mice, fixed, and paraffin-embedded for sectioning into 4-microns thick sections with Epredia™ HM 355S Automatic Microtome.
Animals
All animal work was performed in accordance with protocols approved by the Institutional Animal Care and Use Committee (IACUC) at Stanford University, the USAMRMC Animal Care and Use Review (ACURO), and the laws and regulations of the Department of Agriculture in the United States.
Immunohistochemistry (IHC)
All tumours used for IHC were sectioned to 4 microns in thickness from formalin-fixed, paraffin-embedded tissues. The antibody used for ACAA2 staining was purchased from Abcam (ab128929, 1:100 dilution). The antibody used for CHGA staining was purchased from Santa Cruz Biotechnology (sc-393941, 1:100 dilution). The sections were deparaffined for an hour in a heated chamber at 65 °C. Then, rehydrated in Clearify for 15 min, 100% ethanol for 10 min, 95% ethanol for 10 min, 70% ethanol for 5 min, and water for 10 minutes. Then, antigen retrieval was performed by immersing the slides in 95 °C, 10 mM citrate buffer (pH = 6.0) for 30 min. After cooling the slides to room temperature, tissues were covered in 3% hydrogen peroxide for 5 min to block endogenous peroxidase activity. Slides were then blocked with 2.5% horse serum diluted in 1xPBS for an hour in a humidified chamber under room temperature. After blocking, sections were incubated overnight with biotin-conjugated primary anti-ACAA2 antibody at 4 °C (1:100 dilution in blocking solution). The next day, slides were washed three times with 1XPBS and incubated with streptavidin-horseradish peroxidase (SA-5004, 1:200, Vector Laboratories) for an hour at room temperature. After washing the slides three times in 1XPBS again, a DAB substrate kit (Dako, as per the manufacturer’s protocol) was used to visualise the staining signal. The sections were then stained with hematoxylin and dehydrated. After mounting and adding coverslips to the slides, all slides were scanned using a NanoZoomer (Hamamatsu).
Tissue microarrays (TMAs) and patient tissue samples
The patient TMAs with benign and localised prostate cancer cores was constructed at Stanford University, Department of Urology. ACAA2 staining on these TMAs included 35 patients with benign prostate (101 cores) and 18 patients with localised prostate cancer (50 cores). All sample collection was approved by the Institutional Review Board (IRB), and informed consent was provided by all patients under the protocol number IRB: 5628. The LuCaP prostate cancer patient-derived xenograft (PDX) TMA was constructed at the University of Washington. 38 models are present on this TMA, with three cores of three different tumours of each model. ACAA2 staining on this PDX TMAs included 29 adeno-CRPC PDXs with 86 cores and 9 NEPC PDXs with 27 cores. Cores that were damaged or lost during IHC staining were excluded. 10 SCLC, 12 lung carcinoid, and 15 lung adenocarcinoma patient tumour samples were purchased from the Stanford Cancer Institute (SCI) Tissue Bank, and the diagnoses were validated by pathologists. Informed consent was provided by all patients for sample collection under the approved IRB protocol (IRB: 11977). ACAA2 staining in 20 NE neoplasms from 9 organs (mediastinum, cardia, gallbladder, colon, small intestine, pancreas, rectum, stomach, and lung), 16 adenocarcinomas, and 8 normal tissues were performed on an TMA (2 cores per case) purchased from tissuearray.com (#NE921). All staining was scored without awareness of patient clinical information on an intensity-based scale from 0 to 3 (0 is negative, 1 is low, 2 is medium, and 3 is high). All statistical significance was obtained through z-score calculator for 2 population proportions (https://www.socscistatistics.com/tests/ztest/) between a group with scores 0 and 1(negative to low intensity) and a group with scores 2 and 3 (medium to high intensity).
Analysis of ACAA2 mRNA levels in patient datasets
ACAA2 mRNA levels across various cancer cell lines were assessed via Cancer Cell Line Encyclopaedia (CCLE) [34]. ACAA2 mRNA levels were also assessed from 5 independent, previously published datasets: 3 for prostate cancer patients [35,36,37] and 2 for lung cancer patients [38, 39]. Data were accessed via cBioPortal for Cancer Genomics (https://www.cbioportal.org). The ACAA2 mRNA expression z-scores relative to all samples were obtained from the datasets, and data analysis was performed via Prism 9.0 software. Student’s t-test was performed to compare the ACAA2 mRNA levels in these two groups. For the Abida et al. (2019) dataset, AR scores and NEPC scores were used to sort patients into NEPC and CRPC groups [36]. The top 30 patients with the highest NEPC score and the lowest AR score were determined into the NEPC group, and the top 30 patients with the lowest NEPC score and the highest AR score were characterised into the adeno-CRPC group (Supplementary Fig. S1C). ACAA2 mRNA z-scores between lung adenocarcinoma and SCLC in the Rohrbeck et al. (2008) dataset, and ACAA2 mRNA expression between normal lung, lung adenocarcinoma, and SCLC were compared in the Bhattacharjee et al. (2001), dataset. All patient groups were assumed to follow a normal distribution. Information on patient exposure to platinum-based therapy was also utilised from the Rohrbeck et al. (2008) dataset. Samples where ACAA2 mRNA expression information is not available are excluded from the analysis.
Overall survival
Kaplan–Meier curve in lung adenocarcinoma was plotted with data from KM Plotter (https://kmplot.com/analysis/) [40]. Kaplan–Meier curve in neuroblastoma was generated via Prism 9.0. Patient overall survival and ACAA2 mRNA expression were obtained from Target, 2018 (phs000467.v21.p8) through cBioPortal for Cancer Genomics. Hazard ratio with confidence intervals and Log-rank P-values (Mantel-Cox test) were calculated. ACAA2 high and low groups were sorted using the median ACAA2 expression as the threshold for cut-off.
Statistical analysis
When comparing the statistical significance between two groups, Student’s t-test was performed on Prism 9.0 software. All t-tests were two-tail, unpaired, and parametric, and P-values of 0.05 or less were considered statistically significant (*P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns = non-significant). Significance levels for contingency plots were obtained as z-score for 2 populations proportions via online calculators (socscistatistics.com).
Results
ACAA2 protein level is elevated in NEPC
ACAA2 expression was significantly elevated (P = 5.9*10-6) in TD-NEPC tumours with a fold-change of 3 (Fig. 1a) relative to the control, non-SCNC LNCaP tumours in analysis of previously published proteomic profiling [26]. ACAA2 mRNA expression was also elevated in the NEPC cell line, NCI H660, relative to non-SCNC prostate cancers when assessing cell line mRNA levels using data from the Cancer Cell Line Encyclopaedia (CCLE) (Fig. 1b) [34]. To assess the correlation of ACAA2 with prostate cancer malignancy, western blot (WB) was performed to assess ACAA2 protein expression (Fig. 1c). We also generated tumour xenografts from the same cell lines and performed immunohistochemistry (IHC) analysis. WB and IHC results indicated that ACAA2 protein level positively correlated with SCNC phenotypes as ACAA2 was highly expressed in both NEPC strains (H660 and TD-NEPC) (Fig. 1c, d). ACAA2 was also expressed in DU145 and PC3 xenografts, both of which exhibit AR loss and are, therefore, resistant to androgen deprivation therapies (Fig. 1c, d). DU145 has recently been characterised as double-negative prostate cancer (DNPC), which, like NEPC, also stems from CRPC and occurs in 20% to 15% of metastatic CRPC cases [15]. DNPC is highly aggressive due to enhanced metastasis and stemness signature, and treatment options remain limited [15]. We also observed that ACAA2 was expressed in ARCaP, which is an AR-low, androgen-repressed prostate cancer cell line that exhibits increased metastatic potential to bones [41, 42]. WB and IHC results consistently demonstrated high ACAA2 expression in the NEPC cell lines H660 and TD-NEPC (Fig. 1c, d). In addition, increased ACAA2 expression also corresponded with increases in standard NE markers, SYP, CD56, and CHGA, in two published mCRPC datasets (Supplementary Fig. S1A, B). In both the Abida et al. (2019) and the Nguyen H. et al. (2017) datasets, our results demonstrated a significant positive correlation between ACAA2, SYP (P = 0.0002, 0.0044), CD56 (P = 0.001), and CHGA (P = 0.0001, 0.0087) (Supplementary. Fig. S1A, B). These results suggest an association between ACAA2 expression and the NE phenotype.
High levels of ACAA2 correlate with prostate cancer progression in patient samples
To validate the positive correlation between ACAA2 expression and the NE phenotype, we analysed three published patient datasets via cBioPortal, and compared ACAA2 mRNA expression in NEPC and adeno-CRPC tumours. ACAA2 levels were significantly elevated in NEPC patient groups relative to adeno-CRPC patient groups from all three datasets, including Beltran et al. (2016) (P = 8.2*10-3), Abida et al. (2019) (P = 5.6*10-4), and Nguyen et al. (2017) (P = 9.3*10-3) (Fig. 2a and Supplementary Fig. S1B, C). These results implicated ACAA2 as a candidate molecular indicator for the SCNC phenotype and suggested a positive association between ACAA2 expression and prostate cancer progression. In addition, patient samples from the Abida (2019) [36] dataset were sorted based on the metastatic site, and samples from each site were then compared to localised prostate cancer samples. There was a significant increase of ACAA2 mRNA expression in samples from liver metastasis when compared to samples from localised prostate cancer (Fig. 2b). Studies have shown that the prevalence of liver metastasis is increased in NEPC patients and correlates with reduced overall survival in CRPC patients [43]. The correlation between ACAA2 expression and increased liver metastasis further suggests its association with the aggressive clinical course observed in NEPC patients.
To assess the profile of ACAA2 expression in prostate cancer tumours, we stained patient tissue microarrays (TMAs) for ACAA2 (Fig. 3a, b). Two TMAs were utilised: one containing benign prostate cores and localised prostate cancer cores (35 patients/101 cores with benign prostate; 18 patients/50 cores with localised prostate cancer), and another containing adeno-CRPC and NEPC PDX cores (29 PDX/ 86 cores with adeno-CRPC; 9 PDX/27 cores with NEPC). IHC revealed that ACAA2 was selectively expressed in cancerous cores relative to benign cores (Supplementary Fig. S2). Only 2 out of the 101 (1.98%) normal prostate cores stained positive (staining intensity score >= 1) for ACAA2 while 93 of the 163 (57%) prostate cancer cores (including localised, adeno-CRPC, and NEPC) stained positive for ACAA2 (P < 10-4), demonstrating ACAA2’s selective elevation in cancerous phenotypes (Supplementary Fig. S2). Importantly, ACAA2 staining from PDX TMAs of NEPC and adeno-CRPC tumours revealed an increase in ACAA2 protein levels in NEPC when compared to adeno-CRPC PDXs (Fig. 3b–c). Only 33% (28 out of 86) of adeno-CRPC cores stained with medium/high intensity (intensity scores of 2 and 3) for ACAA2, while 78% (21 out of 27) of NEPC cores stained medium/high for ACAA2 (Fig. 3c). None of the benign prostate tissues, only 2 out of 50 (4%) localised prostate cancer samples, and 10 out of 86 (12%) in adeno-CRPC stained high for ACAA2, which is significantly lower than the 11 out of 27 (41%) of NEPC samples (Fig. 3c). This indicates that ACAA2 level is upregulated in patients with more advanced prostate cancers and positively correlates with prostate cancer progression. IHC results also indicate that protein expression of ACAA2 positively associates with protein levels of NE markers: CHGA (P = 3.95*10-2) and SYP (P = 8.3*10-3), which further supports the correlation between elevated ACAA2 protein expression and the SCNC phenotype (Supplementary Fig. S3).
ACAA2 expression is elevated in other SCNCs
We identified that ACAA2 protein expression is also elevated in NE cell lines IMR32 (neuroblastoma), H82 (SCLC), and H29 (SCLC) measured by WB (Fig. 4a). All non-small-cell lung cancer (NSCLC) cell lines, including H1650 and H358, exhibited undetectable levels of ACAA2 by WB (Fig. 4a). We also assessed ACAA2 mRNA levels in CCLE [34] to demonstrate that ACAA2 mRNA expression is also significantly increased in SCLC (N = 50) and neuroblastoma cell lines (N = 16), both of which are NE cancers, relative to their non-NE counterparts: NSCLC (N = 120) and glioma (N = 53) (Fig. 4b and Supplementary Fig. S4A, B). While glioma is not derived from the same tissue of origin as neuroblastoma, it has been used as a non-NE comparator for neuroblastoma [19, 44]. When compared to glioma, ACAA2 expression level in neuroblastoma was significantly elevated (P = 2.5*10-6) (Fig. 4b). The same trend was observed in SCLC relative to NSCLC with P = 5.7*10-15 (Fig. 4b). Then, IHC was performed on neuroblastoma, SCLC, and NSCLC tumour xenografts and demonstrated enhanced expression of ACAA2 in neuroblastoma and SCLC relative to NSCLC (Fig. 4c).
The correlation between ACAA2 and the SCNC phenotype was further confirmed via ACAA2 mRNA level analysis in two independent lung cancer patient datasets (Fig. 4d) [38, 39]. SCLC exhibited significantly elevated ACAA2 mRNA expressions when compared to lung adenocarcinoma [P = 2.52*10-5 (left panel); 7.2*10-7 (right panel)] and normal lung tissues (P = 2.2*10-4), which further suggests a positive correlation between ACAA2 expression and SCNCs (Fig. 4d). In addition, consistent with the relationship observed in prostate cancer, ACAA2 mRNA expression also positively correlated with expressions of CHGA and CD56 (Supplementary Fig. S5). In Rohrbeck et al. (2008) dataset, increased ACAA2 correlated with the SCLC phenotype relative to lung adenocarcinoma as well as an increased expression of NE markers CHGA (P = 9.5*10-3) and CD56 (P = 3.81*10-2) (Supplementary Fig. S5A). This is also observed in the Bhattacharjee et al. (2001) dataset, with P < 10-4 for both positive correlations between ACAA2, CHGA, and SYP (Supplementary Fig. S5B).
To assess the clinical relevance of the correlation between ACAA2 and SCNC phenotypes, IHC staining of ACAA2 in lung adenocarcinoma patient tumour (N = 15) was compared to ACAA2 staining in patient samples from lung carcinoid tumour (N = 12) and SCLC (N = 10), both of which exhibit NE phenotypes (Fig. 5a–d). Using a 0 to 3 intensity scale (Fig. 5a), we discovered an increase of ACAA2 expression in lung carcinoid (P = 0.033) and SCLC (P = 0.034), relative to the non-NE, adenocarcinoma patient samples (Fig. 5b, c). The elevation of ACAA2 in NE lung cancers was further confirmed in the contingency plot of intensity scores (Fig. 5d). Compared to lung adenocarcinoma where 40% (6/15) of cases stained with medium/high intensity, 83% (10/12) of lung carcinoid tumours stained with medium/high intensity (P = 10-5) (Fig. 5d). The same trend was observed in SCLC, where 90% (9/10) of SCLC stained with medium/high intensity (Fig. 5d). This elevation suggests a correlation between ACAA2 levels and NE features in clinical patient samples. To explore ACAA2’s expression in other tumour types with NE features, we stained ACAA2 in a TMA (NE921) with 20 tumours with NE features, 16 adenocarcinomas, and 8 normal cases (Supplementary Fig. S6). While ACAA2 was detected in cases with NE features, there was no significant difference in ACAA2 intensity relative to normal and adenocarcinoma groups (Supplementary Fig. S6). This could be the result of a small number of samples or differences in primary sites. Further exploration in larger cohorts will be necessary to validate the trend and to elucidate the differences between ACAA2 expression in various primary sites.
Lastly, we assessed whether increased ACAA2 expression is associated with patient clinical prognosis. We discovered that ACAA2 expression is lower in lung cancer patients who were exposed to platinum-based therapy relative to non-treated patients, and that increased ACAA2 was associated with worse overall survival in lung adenocarcinoma (P = 2.2*10-4) and neuroblastoma patients (P = 2.77*10-2) (Fig. 6). Based on these results, we hypothesise that increased ACAA2 is associated with worse clinical outcome. Exploration of this association in additional patient cohorts to elucidate the clinical potential of ACAA2 will be critical to the translation of this knowledge into clinics.
Discussion
Based on our result, we hypothesise that ACAA2 has the potential to differentiate cancers with NE features from their non-NE counterparts in SCNCs like NEPC and SCLC. In addition, our study suggests the role of ACAA2 in prostate cancer disease progression and its potential as a therapeutic target for advanced, metastatic prostate cancers.
SCNCs exhibit similar molecular profiles and genetic alterations, suggesting a common pathway of transdifferentiation in multiple cancers [1, 4, 5]. Published studies have shown that converging genetic expression profiles are observed as cancers progress into the SCNC phenotype [4]. For instance, loss of REST transcriptional repression, increased EZH2, amplified MYCN, loss of TP53, and loss of RB1 have been suggested to foster the SCNC phenotype across multiple tissue sites [35, 45, 46].
Currently, the survival rate for patients with SCNCs remains low due to their therapy resistance and the extensive metastasis that is a hallmark of SCNCs and contributes to its worse clinical outcome [4]. The platinum and etoposide-based chemotherapies that form the frontline of SCNC treatments show short-term clinical effects on patient survival [1, 4, 5]. As a result, there is an urgent need to identify pathways crucial for NE transdifferentiation in order to discover novel therapeutic targets to broaden the treatment options for this lethal disease.
Since ACAA2 is overexpressed in various types of SCNCs and is also upregulated by Trop2-driven NE transdifferentiation, ACAA2 might play a role in NE progression to SCNCs. ACAA2 is a key enzyme in the mitochondrial fatty acid beta-oxidation pathway [27,28,29]. As ACAA2 is consistently elevated in NEPC and SCLC, we propose the possibility of a linkage between ACAA2, fatty acid beta-oxidation, and NE progression. Thus, the inhibition of ACAA2 may have therapeutic benefits in NE cancers. In fact, a previous study suggested a shared sensitivity towards the disruption of lipid metabolism in SCNCs [4]. Currently, there is a pharmacological ACAA2 inhibitor, trimetazidine hydrochloride, that is currently used to treat angina pectoris and myocardial ischaemia as an anti-ischaemic (anti-anginal) metabolic agent in Europe [47]. As an identified fatty acid oxidation inhibitor, trimetazidine was shown to elevate myocardial glucose metabolism and to increase glucose level during ischaemia through the inhibition of fatty acid metabolism [47,48,49]. Various studies have also demonstrated that the inhibition of fatty acid beta-oxidation via trimetazidine enhances glucose oxidation [47, 50, 51]. Our study supports further exploration of this ACAA2 inhibitor to test its therapeutic efficacy against NEPC and SCLC.
Our study demonstrates that ACAA2 expression is elevated in cancers with NE phenotype through assessing the expression profile of ACAA2 in cell lines and xenografts of neuroblastoma as well as cell lines, xenografts, patient mRNA, and patient tissue samples from prostate and lung cancers. This study supports further assessment of ACAA2 expression profile in larger, independent patient cohorts across various types of SCNCs to further delineate its candidacy as a molecular indicator for SCNCs and a potential therapeutic target.
Data availability
All data used in this publication can be found in the methods section, figures, or supplementary information.
References
Rickman DS, Beltran H, Demichelis F, Rubin MA. Biology and evolution of poorly differentiated neuroendocrine tumors. Nat Med. 2017;23:1–10.
Hallet J, Law CH, Cukier M, Saskin R, Liu N, Singh S. Exploring the rising incidence of neuroendocrine tumors: a population-based analysis of epidemiology, metastatic presentation, and outcomes. Cancer. 2015;121:589–97.
George J, Lim JS, Jang SJ, Cun Y, Ozretic L, Kong G, et al. Comprehensive genomic profiles of small cell lung cancer. Nature. 2015;524:47–53.
Balanis NG, Sheu KM, Esedebe FN, Patel SJ, Smith BA, Park JW, et al. Pan-cancer convergence to a small-cell neuroendocrine phenotype that shares susceptibilities with hematological malignancies. Cancer Cell. 2019;36:17–34.e7.
Klimstra DS, Beltran H, Lilenbaum R, Bergsland E. The spectrum of neuroendocrine tumors: histologic classification, unique features and areas of overlap. Am Soc Clin Oncol Educ Book. 2015;35:92–103.
Park JW, Lee JK, Sheu KM, Wang L, Balanis NG, Nguyen K, et al. Reprogramming normal human epithelial tissues to a common, lethal neuroendocrine cancer lineage. Science. 2018;362:91–5.
Wang Y, Wang Y, Ci X, Choi SYC, Crea F, Lin D, et al. Molecular events in neuroendocrine prostate cancer development. Nat Rev Urol. 2021;18:581–96.
Malta TM, Sokolov A, Gentles AJ, Burzykowski T, Poisson L, Weinstein JN, et al. Machine learning identifies stemness features associated with oncogenic dedifferentiation. Cell. 2018;173:338–54.e15.
Smith BA, Balanis NG, Nanjundiah A, Sheu KM, Tsai BL, Zhang Q, et al. A human adult stem cell signature marks aggressive variants across epithelial cancers. Cell Rep. 2018;24:3353–66.e5.
Davies AH, Beltran H, Zoubeidi A. Cellular plasticity and the neuroendocrine phenotype in prostate cancer. Nat Rev Urol. 2018;15:271–86.
Teo MY, Rathkopf DE, Kantoff P. Treatment of advanced prostate cancer. Annu Rev Med. 2019;70:479–99.
Komura K, Sweeney CJ, Inamoto T, Ibuki N, Azuma H, Kantoff PW. Current treatment strategies for advanced prostate cancer. Int J Urol. 2018;25:220–31.
Vlachostergios PJ, Puca L, Beltran H. Emerging variants of castration-resistant prostate cancer. Curr Oncol Rep. 2017;19:32.
Labrecque MP, Coleman IM, Brown LG, True LD, Kollath L, Lakely B, et al. Molecular profiling stratifies diverse phenotypes of treatment-refractory metastatic castration-resistant prostate cancer. J Clin Invest. 2019;129:4492–505.
Bluemn EG, Coleman IM, Lucas JM, Coleman RT, Hernandez-Lopez S, Tharakan R, et al. Androgen receptor pathway-independent prostate cancer is sustained through FGF signaling. Cancer Cell. 2017;32:474–89.e6.
Conteduca V, Oromendia C, Eng KW, Bareja R, Sigouros M, Molina A, et al. Clinical features of neuroendocrine prostate cancer. Eur J Cancer. 2019;121:7–18.
Ather MH, Abbas F, Faruqui N, Israr M, Pervez S. Correlation of three immunohistochemically detected markers of neuroendocrine differentiation with clinical predictors of disease progression in prostate cancer. BMC Urol. 2008;8:21.
Sarhadi VK, Armengol G. MoleculaR Biomarkers in Cancer. Biomolecules. 2022;12:1021.
Guo H, Ci X, Ahmed M, Hua JT, Soares F, Lin D, et al. ONECUT2 is a driver of neuroendocrine prostate cancer. Nat Commun. 2019;10:278.
Park JW, Lee JK, Witte ON, Huang J. FOXA2 is a sensitive and specific marker for small cell neuroendocrine carcinoma of the prostate. Mod Pathol. 2017;30:1262–72.
Beltran H, Oromendia C, Danila DC, Montgomery B, Hoimes C, Szmulewitz RZ, et al. A phase II trial of the aurora kinase a inhibitor alisertib for patients with castration-resistant and neuroendocrine prostate cancer: efficacy and biomarkers. Clin Cancer Res. 2019;25:43–51.
Kolla BC, Racila E, Patel MR. Deep and prolonged response to aurora a kinase inhibitor and subsequently to nivolumab in MYCL1-driven small-cell lung cancer: case report and literature review. Case Rep. Oncol Med. 2020;2020:8026849.
Du R, Huang C, Liu K, Li X, Dong Z. Targeting AURKA in cancer: molecular mechanisms and opportunities for cancer therapy. Mol Cancer. 2021;20:15.
Zhang Y, Zheng D, Zhou T, Song H, Hulsurkar M, Su N, et al. Androgen deprivation promotes neuroendocrine differentiation and angiogenesis through CREB-EZH2-TSP1 pathway in prostate cancers. Nat Commun. 2018;9:4080.
Dardenne E, Beltran H, Benelli M, Gayvert K, Berger A, Puca L, et al. N-Myc induces an EZH2-mediated transcriptional program driving neuroendocrine prostate cancer. Cancer Cell. 2016;30:563–77.
Hsu EC, Rice MA, Bermudez A, Marques FJG, Aslan M, Liu S, et al. Trop2 is a driver of metastatic prostate cancer with neuroendocrine phenotype via PARP1. Proc Natl Acad Sci USA. 2020;117:2032–42.
Tomilov A, Tomilova N, Shan Y, Hagopian K, Bettaieb A, Kim K, et al. p46Shc inhibits thiolase and lipid oxidation in mitochondria. J Biol Chem. 2016;291:12575–85.
Raaka BM, Lowenstein JM. Inhibition of fatty acid oxidation by 2-bromooctanoate. Evidence for the enzymatic formation of 2-bromo-3-ketooctanoyl coenzyme A and the inhibition of 3-ketothiolase. J Biol Chem. 1979;254:6755–62.
Zhang Y, Wang Y, Wang X, Ji Y, Cheng S, Wang M, et al. Acetyl-coenzyme A acyltransferase 2 promote the differentiation of sheep precursor adipocytes into adipocytes. J Cell Biochem. 2019;120:8021–31.
Shen X, Zheng S, Thongboonkerd V, Xu M, Pierce WM Jr, Klein JB, et al. Cardiac mitochondrial damage and biogenesis in a chronic model of type 1 diabetes. Am J Physiol Endocrinol Metab. 2004;287:E896–905.
Kuhlow D, Zarse K, Voigt A, Schulz TJ, Petzke KJ, Schomburg L, et al. Opposing effects of dietary sugar and saturated fat on cardiovascular risk factors and glucose metabolism in mitochondrially impaired mice. Eur J Nutr. 2010;49:417–27.
Chen MC, Chang JP, Lin YS, Pan KL, Ho WC, Liu WH, et al. Deciphering the gene expression profile of peroxisome proliferator-activated receptor signaling pathway in the left atria of patients with mitral regurgitation. J Transl Med. 2016;14:157.
Yang Y, Fang X, Yang R, Yu H, Jiang P, Sun B, et al. MiR-152 regulates apoptosis and triglyceride production in MECs via targeting ACAA2 and HSD17B12 genes. Sci Rep. 2018;8:417.
Ghandi M, Huang FW, Jane-Valbuena J, Kryukov GV, Lo CC, McDonald ER 3rd, et al. Next-generation characterization of the Cancer Cell Line Encyclopedia. Nature. 2019;569:503–8.
Beltran H, Prandi D, Mosquera JM, Benelli M, Puca L, Cyrta J, et al. Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. Nat Med. 2016;22:298–305.
Abida W, Cyrta J, Heller G, Prandi D, Armenia J, Coleman I, et al. Genomic correlates of clinical outcome in advanced prostate cancer. Proc Natl Acad Sci USA. 2019;116:11428–36.
Nguyen HM, Vessella RL, Morrissey C, Brown LG, Coleman IM, Higano CS, et al. LuCaP prostate cancer patient-derived xenografts reflect the molecular heterogeneity of advanced disease an-d serve as models for evaluating cancer therapeutics. Prostate. 2017;77:654–71.
Rohrbeck A, Neukirchen J, Rosskopf M, Pardillos GG, Geddert H, Schwalen A, et al. Gene expression profiling for molecular distinction and characterization of laser captured primary lung cancers. J Transl Med. 2008;6:69.
Bhattacharjee A, Richards WG, Staunton J, Li C, Monti S, Vasa P, et al. Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses. Proc Natl Acad Sci USA. 2001;98:13790–5.
Gyorffy B, Surowiak P, Budczies J, Lanczky A. Online survival analysis software to assess the prognostic value of biomarkers using transcriptomic data in non-small-cell lung cancer. PLoS ONE. 2013;8:e82241.
Lo UG, Chen YA, Khamis ZI, Kao WH, Hsieh JT, Sang QA. Studies of hormonal regulation, phenotype plasticity, bone metastasis, and experimental therapeutics in androgen-repressed human prostate cancer (ARCaP) model. Am J Clin Exp Urol. 2021;9:277–86.
Zhau HY, Chang SM, Chen BQ, Wang Y, Zhang H, Kao C, et al. Androgen-repressed phenotype in human prostate cancer. Proc Natl Acad Sci USA. 1996;93:15152–7.
Halabi S, Kelly WK, Ma H, Zhou H, Solomon NC, Fizazi K, et al. Meta-analysis evaluating the impact of site of metastasis on overall survival in men with castration-resistant prostate cancer. J Clin Oncol. 2016;34:1652–9.
Almstedt E, Elgendy R, Hekmati N, Rosen E, Warn C, Olsen TK, et al. Integrative discovery of treatments for high-risk neuroblastoma. Nat Commun. 2020;11:71.
Nadal R, Schweizer M, Kryvenko ON, Epstein JI, Eisenberger MA. Small cell carcinoma of the prostate. Nat Rev Urol. 2014;11:213–9.
Lim JS, Ibaseta A, Fischer MM, Cancilla B, O’Young G, Cristea S, et al. Intratumoural heterogeneity generated by Notch signalling promotes small-cell lung cancer. Nature. 2017;545:360–4.
Lopaschuk GD, Barr R, Thomas PD, Dyck JR. Beneficial effects of trimetazidine in ex vivo working ischemic hearts are due to a stimulation of glucose oxidation secondary to inhibition of long-chain 3-ketoacyl coenzyme a thiolase. Circ Res. 2003;93:e33–7.
Glezer MG, Vygodin VA, Investigators ODA. Anti-anginal effectiveness and tolerability of trimetazidine modified release 80 mg once daily in stable angina patients in real-world practice. Adv Ther. 2018;35:1368–77.
Glezer MG, Vygodin VA, Investigators ODA. Effectiveness of trimetazidine in patients with stable angina pectoris of various durations: results from ODA. Cardiol Ther. 2020;9:395–408.
Kantor PF, Lucien A, Kozak R, Lopaschuk GD. The antianginal drug trimetazidine shifts cardiac energy metabolism from fatty acid oxidation to glucose oxidation by inhibiting mitochondrial long-chain 3-ketoacyl coenzyme A thiolase. Circ Res. 2000;86:580–8.
Lee L, Horowitz J, Frenneaux M. Metabolic manipulation in ischaemic heart disease, a novel approach to treatment. Eur Heart J. 2004;25:634–41.
Acknowledgements
This study was made possible by the support and guidance of fellow members of the Stoyanova Lab. We are grateful to the Canary Centre for Cancer Early Detection at Stanford University and the Department of Molecular and Medical Pharmacology and the Department of Urology at the University of California, Los Angeles for providing the infrastructure under which this study was executed.
Funding
TS is supported by the National Institutes of Health (NIH)/National Cancer Institute (NCI) (R37CA240822, R01CA244281, P50CA092131, and R01CA274978) and by the United States Department of Defence (Award Number HT9425-23-1-1034). JDB is supported by NIH CA229933 and NIH CA196387. The establishment and characterisation of the LuCaP PDX models have been supported by the PNW Prostate Cancer SPORE P50CA097186 and P01CA163227. The opinions and recommendations expressed in this article belong to the authors and are not necessarily endorsed by the funding agencies.
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MS, SL, and TS: conceptualisation and methodology. MS, SL, ECH, BRA, MA, and CJS: experimentation. AT, HMN, CJS, RN, CS, JH, JDB, and EC: contributed samples. MS, SL, ECH, CJS, CS, JH, and TS: data analysis and interpretation. MS: figures and manuscript. SL, BRA, ABH, CS, JH, JDB, EC, TS: manuscript editing. TS, SL: supervision. All authors reviewed the manuscript.
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TS is a consultant for Dren Bio, Inc. EC obtains funding from Genentech, Sanofi, AbbVie, Astra Zeneca, Foghorn Pharmaceuticals, Kronos Bio, MacroGenics, Janssen Research, Bayer Pharmaceuticals, Forma Pharmaceuticals, Gilead, Zenith Epigenetics and is a consultant of DotQuant.
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The collection of the tissues to construct the prostate cancer TMAs utilised for this study was reviewed and approved by the Research Compliance Office (IRB: 5628) at Stanford University. The collection of the lung cancer patient tissues utilised in this study was performed under informed consent and under the approved IRB protocol (IRB: 11977) at Stanford Cancer Institute. All methods were conducted under the guidance of ethical guidelines and relevant regulations from the Regional Ethics Committee.
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Shen, M., Liu, S., Toland, A. et al. ACAA2 is a novel molecular indicator for cancers with neuroendocrine phenotype. Br J Cancer 129, 1818–1828 (2023). https://doi.org/10.1038/s41416-023-02448-y
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DOI: https://doi.org/10.1038/s41416-023-02448-y