In vitro-based search for promising anti-cancer drug combinations may provide important leads to improved cancer therapies. Currently there are no integrated computational-experimental methods specifically designed to search for combinations, maximizing a predefined therapeutic index (TI) defined in terms of appropriate model systems. Here, such a pipeline is presented allowing the search for optimal combinations among an arbitrary number of drugs while also taking experimental variability into account. The TI optimized is the cytotoxicity difference (in vitro) between a target model and an adverse side effect model. Focusing on colorectal carcinoma (CRC), the pipeline provided several combinations that are effective in six different CRC models with limited cytotoxicity in normal cell models. Herein we describe the identification of the combination (Trichostatin A, Afungin, 17-AAG) and present results from subsequent characterisations, including efficacy in primary cultures of tumour cells from CRC patients. We hypothesize that its effect derives from potentiation of the proteotoxic action of 17-AAG by Trichostatin A and Afungin. The discovered drug combinations against CRC are significant findings themselves and also indicate that the proposed strategy has great potential for suggesting drug combination treatments suitable for other cancer types as well as for other complex diseases.
The development of a malignant tumour is generally associated with great complexity at the molecular level including the rewiring of different signal transduction pathways and biochemical feedback loops. This fact has made it widely accepted that in many cases a single drug treatment cannot produce the desired therapeutic effect1,2. Drug combinations are attractive owing to their lower propensity to trigger drug resistance (due to non-overlapping mechanisms of action) and side effects including adverse actions (due to lower dosage levels)3,4. Moreover, the use of combinations includes prospects of replacing some of the current, most expensive anti-cancer therapies by much cheaper drug cocktails. However, the huge space of possible compound mixtures is still largely unexplored and there is currently very slow progress in discovering novel, successful combination therapies for cancer.
A few combinations are indeed frequently used in the treatment of cancer, but such regimens are mostly based on empirical observations with agents already known to be effective in the disease rather than on well-defined and valid design criteria. The quite limited combination testing performed so far has covered a tiny fraction of all possible combinations and is therefore unlikely to result in selection of the optimal combinations among the huge number of possibilities5,6,7. Even in the current era of high throughput screening (HTS), the greatest challenge to achieve a successful, cost-effective search is the exponential growth in the possible number of drug and concentration combinations. Therefore, a procedure for successful discovery of multi-component therapies requires an semi-automated pipeline of the kind illustrated in Fig. 1A that involves integrated large-scale automated procedures and experimental readouts.
A few iterative computational-experimental procedures have recently been proposed that allow search in arbitrarily large combination spaces8,9,10. The general approach is illustrated in Fig. 1A. However, these seminal efforts do not provide any method designed explicitly to maximize a predefined therapeutic index (TI) that quantifies the desired effect versus the adverse side effects. In addition, the reported efforts are based on manual iterations rather than a semi-automated approach suitable for large scale experimentation.
In cancer pharmacology research, in vitro cancer cell line models are typically used with cytotoxicity or inhibition of proliferation as the primary read-out. For evaluation of drug combination effects, the current state-of-the-art uses a measure of synergy as endpoint because total cell kill is always trivially increased by adding another drug with cytotoxic action to a combination. Synergy as per classical definition is the improvement in efficacy over a theoretical model of expected joint action11. In the context of cancer, this stands in stark contrast to combination therapies used in clinical practice. Although there are some exceptions based on modern targeted drugs, still many anti-cancer combination therapies in use are not designed based on a synergistic interaction but from observed clinical utility in terms of increased survival. By using drugs with different side-effect spectrums, total dose can be increased while having limited side-effects. As already mentioned, the combination therapies are also attractive because they reduce the risk of emergent drug resistance. Neither of these two underpinnings of anti-cancer combination therapies are addressed by the use of classic measures of synergy. Thus a new principle for preclinical development of clinically relevant combination therapies could prove useful.
Here we report results from developing and employing a novel, semi-automatic, iterative search method that aims at finding optimal drug combinations for oncological targets that are maximising a clinically motivated TI. The TI serves as a proxy for the therapeutic benefit of a combination; an optimal combination should inhibit the cancer cells while least affecting healthy cells. The TI used is the differential cytotoxic action (in terms of cell viability) of a combination between cancer cell and normal/reference cell models11. We search for locally optimal drug combinations using an algorithm called MACS (Medicinal Algorithmic Combinatorial Screen)9, significantly improved in this work by taking experimental variability into account. We describe our pipeline in the context of applying it to CRC in vitro models.
Characterisation of five among the most promising drug combinations found by the pipeline suggests that all of them are suitable candidates for the treatment of CRC. One of these combinations, (Trichostatin A, Afungin, 17-AAG), was found to eradicate 6 different CRC model systems with limited side-activity against the normal/reference cells. It is also effective in primary cultures of tumour cells from CRC patients. Taken together, besides the discovery of a promising set of drug combinations for treatment of CRCs, this work provides one of the first successful semi-automated pipelines for discovery of anti-cancer drug combinations of arbitrary size with pronounced activity in vitro. As this method is fully generic, it enables and could inspire large-scale systematic explorations of the space of drug combinations for cancer in general, as well as for other complex diseases.
Materials and Methods
All methods were performed in accordance with relevant guidelines and regulations.
Liquid handling robot and programming environment
For liquid handling we used a Beckman Coulter Biomek 2000 liquid handling robot. We employed the integrated programming language BioScript Pro, a scripting language that is an extension of Tool Command Language (TCL)12. Using BioScript Pro, a “cherry picking” program was developed that takes an Excel file containing a list of desired combinations and their positions on the plate as input and performs the required combinatorial liquid handling. The program used and the associated parameter settings are available in the Supplementary Methods II (section on Beckman Coulter Biomek 2000 cherry picking program).
Thirteen drugs were used for the experiment using the MACS algorithm (first experiment, for details see Supplementary Table S1). These were selected on the basis of their diverse target of action in cancer cells and some of them (5FU, Oxaliplatin) are also clinically relevant. IC20 values (the concentration required to kill and/or inhibit growth of cells by 20% as compared to untreated control wells) of these drugs were estimated from concentration-response curves by using either curve fitting (in cases where the model could be properly fitted), or by manual inspection. Matlab code for estimation of IC20 values is provided in Supplementary Methods II (section on Matlab code for prediction of IC10 and IC20 values from concentration response data). In the main experiment, the following six drugs were used: Mitomycin, Sunitinib, Rapamycin, Trichostatin A, 17-AAG and Afungin. An IC20 value for each drug was calculated from concentration response curves in cell line HCT116 as above except for Afungin where the IC20 values were selected based on concentration-response data from the National Cancer Institute NCI-60 DTP Human Tumour Cell Line Screen (downloaded, Dec 2010: http://dtp.nci.nih.gov/docs/cancer/cancer_data.html). All drugs and their concentrations are shown in Table 1. The stock solution for each drug was prepared at a concentration 40 times higher than the IC20 values, so that desired IC20 concentration was restored in final volume inside wells of destination plates. Stock solutions were prepared in phosphate-buffered saline (PBS) and stored in 1 ml Eppendorf tubes (Eppendorf AG, Hamburg, Germany) at −70 °C until further use.
Human cell lines
In the search using the MACS algorithm (first experiment), two human colorectal adenocarcinoma epithelial cell lines (DLD-1 and DLD-1KRAS/-) were used. These cell lines were obtained from Horizon Discovery Ltd, United Kingdom and cultured in McCoy’s 5A medium. In the main experiment using the TACS algorithm, the CRC cell lines HCT116 and HCT29 were obtained from American Type Culture Collection (ATCC, Rockville, MD) and were cultured in McCoy’s 5A medium. The leukemia cell line CCRF-CEM was a kind gift from WT Beck (Department of Pharmacology, college of Medicine, University of Tennessee, Memphis, TN). The cell line was grown in culture medium RPMI-1640 (HyClone, Northumbria, UK). SW620 was also obtained from ATCC and cultured in RPMI-1640 medium. RKO and HCT116KRAS/- cells were obtained from Horizon Discovery Ltd, United Kingdom and cultured in McCoy’s 5A medium. Normal (non-cancerous) colorectal cell line CCD 841 CoN was obtained from ATCC and cultured in EMEM medium. HCT116 cells labelled with GFP (green fluorescent protein) were obtained from Anticancer Inc (San Diego, CA, USA) and cultured in McCoy’s 5A medium.
Tumour cell samples from patients
Tumour sampling of patients with solid tumours was performed intraoperatively during cancer surgery, whereas leukemia sampling was performed by vein puncture at routine blood sampling. All sampling was approved by the regional (Uppsala University) ethical committee (Dnr 2007/237) and after patient informed consent. Tumour cells from solid tumour tissue were prepared by collagenase digestion as previously described13. Leukemia cells were collected by Ficoll-Hypaque (Pharmacia, Uppsala, Sweden) gradient centrifugation as previously described14. The cells obtained from the leukemic samples were single cells or, for solid tumours, small cell clusters with ≥90% viability and with less than 30% non-malignant cells, as judged by morphological examinations of May-Grunwald-Giemsa-stained cytocentrifugate preparations.
Spheroids were formed using HCT116GFP cell line, as described previously15. Briefly, 10000 cells per well were seeded in 50 ml of fresh medium into 384-well F-bottom Corning Ultra-Low Attachment plates. Spheroids were cultured for 7 days without medium change prior to drug treatment. After treatment, cell viability was assessed by mean spheroid GFP fluorescence measurements, using ArrayScan VTI Reader (Cellomics Inc, Pittsburgh, PA, USA). The assay has been shown suitable for such measurements previously15,16.
Calculation of SI values
The SI (Survival Index) values were calculated using the fluorometric microculture cytotoxic assay (FMCA)17,18 readout. FMCA measures the cell survival by measuring fluorescence. Fluorescence is produced by living cells with intact membranes by hydrolysis of fluorescein diacetate to fluorescein. Denoting the FMCA readout value by the letter R, the SI value is determined as the ratio (Rtreated − Rblank)/(Rctrl − Rblank) where Rtreated denotes the readout for the well containing the treatment used, Rblank is the readout from a well without cells and Rctrl is the readout from a well containing cells but no drugs.
The 95% confidence intervals (CIs) for the mean were determined using the t-distribution. Assuming that the experimental variability is normally distributed, the difference between a pair of TI estimates has a t-distribution with the number of degrees of freedom being dependent on the number of replicates used to obtain the estimates, for details see Supplementary Methods Part III.
mRNA gene expression analysis
Induced gene expression changes in the cell line HCT116 were analyzed using microarrays from Affymetrix ® after standard normalisation and pre-processing of data, for details see Supplementary Data, Gene Expression Data.
Initially, we applied the original MACS algorithm9 to find a drug combination that specifically targets cells that carry the clinically prevalent KRAS mutation in CRC. We used the difference in TI between CRC cell lines DLD-1 and DLD-1KRAS/- as a criterion to maximize. DLD-1 carries the clinically prevalent KRAS mutation whereas DLD-1KRAS/- has had the KRAS allele knocked out. The base set consisted of 13 compounds from different mechanistic classes (for details, see Supplementary Table S1) added at their IC20 concentrations. Generation 0 was initialised with a set of 14 randomly generated combinations (see Supplementary Tables S2). Cytotoxicity was measured by FMCA in both DLD-1 and DLD-1KRAS/- cell lines and the TI of each combination was calculated as the difference TI = SKRAS − SWT. Here SKRAS and SWT denote the SI values for DLD-1KRAS/- and DLD-1 (Wild type), respectively. A high value of TI corresponds to high cell kill in the KRAS mutation carrying cell line but low cell kill in the DLD-1KRAS/- cell line. The single best combination was then used to seed the next generation, using all one-compound perturbations around it. This was iterated until no gain in fitness could be made by such a local move. However, although the algorithm terminated with an optimal combination (see Supplementary Figure S1 and Supplementary Tables S2-S5), after examining this pilot run, it was considered necessary to take experimental variability into account as the TI gain observed between subsequent generations may simply be due to noise (experimental variability).
Thus, we designed a less noise-sensitive procedure called Therapeutic Algorithmic Combinatorial Screen (TACS), see Fig. 1B, where we: (i) Take experimental variability into account in selecting seed combinations in each iteration (ii) Keep not only the best, but also the second best hit in each iteration as seeds to generate the next generation of drug combinations. (iii) Reduce experimental variability by performing the experiment twice for every generation and then determine mean TI values based on the pair of results obtained for each drug combination. (iv) Use a termination criterion that takes the experimental variability into account. (v) Encourage the selection of small combinations consisting of as few drugs as possible.
Instead of applying TACS to the same problem as in the pilot study, we decided to study perhaps an even more clinically interesting problem. Although identification of combinations that have activity exclusively in KRAS mutated cells (as aimed for in the pilot study) would be of outstanding interest, we think it would be even more interesting to find a combination which is designed to eradicate multiple types of CRC while, at the same time, inducing limited side-effects. Therefore, as described next, our main experiment was designed to find combinations with ability to eradicate two different CRC in vitro models while at the same time inducing limited side-effects in a reference/toxicity in vitro model.
Implementation of novel TACS algorihtm
For our main experiment, now using our novel TACS algorithm (see Fig. 1B and Methods), we used two CRC cell lines, HCT116 and HT29 and modeled side-effects by the leukemia cell line CCRF-CEM. Using the same kind of notation as above, the TI used was
where SX denotes the survival index of cell line X.
We hypothesize that the use of multiple (two) disease models in the fitness criterion increases the chance that the optimal drug combinations found will be widely applicable. More tentatively, the use of multiple cancer cell lines can also be regarded as a crude model of clone heterogeneity (although the different cell lines originate from different patients/genotypes). The six compounds used were 17-AAG, Afungin, Mitomycin, Sunitinib, Rapamycin and Trichostatin A, each having a different mechanism of activity (see Table 1, Methods). We initialised the search with 13 randomly selected combinations of the drugs at their IC20 concentrations and then iterated until the TI improvement was less than 1 standard deviation (SD). This search was biased towards small combinations by selecting the smallest combinations among those top-ranked but equal within experimental variability (again, using 1 SD as the criterion). The algorithm converged in two iterations, see Fig. 1C. Note that the optimal combination (Sunitinib, 17-AAG, Afungin, Trichostatin A) was produced by perturbing around the second best combination of generation 0 and would have been left out if only one combination would have been selected from generation 0, see Supplementary Tables S6-S8.
The resulting best combinations, (Sunitinib, 17-AAG, Afungin, Trichostatin A), yielded the fitness value 85 ±6.6 in generation 1, which is greater than the value 67 ± 4.9 obtained for the top hit of generation 0. This clearly suggests that the algorithm has succeeded in improving the TI criterion also when taking experimental variability into account. Furthermore, 5 combinations characterised in more detail were the two top winners from each generation (only five because one combination was the best in two consecutive generations), see Table 2.
Generalisation of results to other concentrations and cell line models
One of the main challenges in anti-cancer drug discovery and cancer therapy is the heterogeneity between and within cancer tumours19. In order to determine to what extent the combinations discovered also are promising according to other CRC models, we performed a full factorial concentration-response study of the selected drug combinations using an extended cell line panel consisting of five CRC cell lines: HCT116, HT29, HCT116KRAS/-, SW620 and RKO. Using the combination (17-AAG, Afungin, Trichostatin A) as one illustrative example (for the other four combinations characterised, see Panels A, B & C of Supplementary Figures S2, S4, S6 & S8), each drug was tested at four different concentrations yielding in total 64 (43) different concentration combinations as shown in Fig. 2B. The tested concentrations were 1/25, 1/5, 1 and 5 times the IC20 concentration used in the iterative search shown in Fig. 1C. The concentrations have been ordered by the fitness (TI) criterion in Eq (1) used by TACS. The heatmap in Fig. 2A shows SI values across the five CRC cell lines and the reference/toxicity model CCRF-CEM (rows) where each column corresponds to one concentration combination. It is evident that the combination effect generalises from the pair HCT116 and HT29 to the new three CRC cell lines HCT116KRAS/-, SW620 and RKO. In particular, it is clear that the drug combination has a stronger effect in the new cell lines HCT116KRAS/-, SW620 and RKO than in the original HCT116 and HT29 used in the iterative search. As the combinations are sorted according to TI, one also finds that the concentration combination used in the iterative search (indicated by the black arrow in panel A) is quite a good choice as only 3 other concentration combinations offered a (marginally) larger TI. However, increasing the concentration further decreased the TI by killing off the CCRF-CEM cells.
We also performed the corresponding full factorial concentration-response study using the normal (non-cancerous) colon cell line CCD 841 CoN and the leukaemia cell line CCRF-CEM. Figure 2C shows the average concentration-response across the five cancer cell lines panel together with SI values for these two cell lines. Clearly, many different concentrations for CCD 841 CoN and CCRF-CEM yielded positive TI values thus offering a promising therapeutic window (TW). It can be noted that TW provided by CCD 841 CoN overlaps with TW provided by CCRF-CEM.
An important indicator of the clinical utility of a drug combination is in vitro therapeutic synergy (TS). As already defined11, a drug combination offers TS if the largest TI it can achieve is larger than what can be obtained using any of its constituent drugs alone. For the drug combination (17-AAG, Afungin, Trichostatin A) we made all 10 possible pairwise comparisons of the effect of the combination in one of the five CRC cell lines with the corresponding effect in one of the two normal/reference/toxicity cell lines. For each of these 10 pairwise drug comparisons the number of concentration combinations found to yield a TI significantly larger than the largest TI produced by any of single drugs was determined (using t-test and a Bonferroni corrected p-value threshold), see Panels D and E of Fig. 2. Each bar indicates the total number of concentration combinations that yielded a significantly higher TI for the drug combination than for any single constituent drug within the concentration range studied. The largest possible number of such local TSs achievable is 48 which would have occurred if every pair tested resulted in a significant local TS. For each bar (pairwise comparison), a p-value was calculated and found to be less than or equal to 10−4. These p-values are associated with a previously developed omnibus test11 specifically designed to avoid the multiple-testing problem via the null hypothesis that there is no TS (thus assuming there is no drug concentration combination that obtains a higher TI than any of the constituent drugs alone). For the other four combinations characterised for TS, see Panels D & E of Supplementary Figures S2 & S8 and Panel D of Supplementary Figures S4 & S6.
Efficacy in primary cultures of tumour cells from CRC patients and in a spheroid microtumour in vitro model
The efficacy of the combination (17-AAG, Afungin, Trichostatin A) was investigated in primary cultures of tumour cells from metastases of n = 11 patients with CRC. For comparison, these data were compared with those of tumour cells from patients with ovarian (n = 9) or kidney (n = 6) cancer as well as in one patient with lymphoma. Cytotoxicity induced by the combination in 2 of the CRC samples is shown in Fig. 3, for results regarding the other four combinations see Supplementary Figures S3, S5, S7 & S9. Due to the limited number of cells available for analysis, for these two samples only three different concentrations were used corresponding to 1/10, 1 and 10 times the concentrations used in the iterative search. A summary of the cytotoxicity induced by the combination in all the samples (ovarian, kidney and CRC) is shown in Supplementary Figure S10. Overall, the CRC samples were more resistant than ovarian and lymphoma samples and essentially as resistant as the kidney cancer samples. This pattern of sensitivity ex vivo in tumour cell samples from patients corresponds well to that of standard cytotoxic drugs used in the clinic20. The activity of the combination differed considerably between the individual CRC samples. This is also in line with the varying sensitivity to standard drugs in patient samples, reflecting the biological heterogeneity between tumour samples from the same tumour types. The difference in sensitivity among the CRC samples was not obviously associated with patient treatment status. Thus, there were both sensitive and resistant samples from treatment naïve and previously treated patients (not shown).
Interestingly, the combination was active at relatively low concentrations of the drug components compared to the concentrations of standard cytotoxic drugs needed to induce significant cytotoxicity in patient tumour cells during identical assay conditions. In the combinations all the three constituent drugs were used at concentrations that correspond to levels below IC20 when used in HCT116 cells. Since primary patient cells generally are more resistant than cell lines, this means that the constituent drugs would have a very limited effect on the patient cells (killing far less than 20% of the cells) if they were to be used individually. Two examples illustrating that patient cells are more resistant can, for example, be found in our previous work11,20. In Fig. 3 of the work by Kashif et al.11, one finds that the IC20 values of the standard drugs 5-FU and Oxaliplatin in HCT116 cells are approximately 30 and 16 μM, respectively, whereas in Fig. 1 of the article by Cashin et al.20 one finds that the corresponding concentrations in primary patient cells are approximately 500 and 30 μM.
Finally, we also performed a concentration-response characterisation of the combination in a GFP-labelled HCT116 spheroidal model (Fig. 4A). Three-dimensional spheroids of cells from the cell line HCT116GFP were created in-house and shown to be generally more resistant to standard cytotoxic drugs than monolayer (2D) cultures15. The spheroids were treated according to a full factorial concentration-response experiment at concentrations 5 times higher than for the 2D models and the resulting SI values were quantified every 24h using measurement of mean spheroid GFP fluorescence. In Fig. 4A, the temporal (3 & 7 days) evolution of the SI values for the combination (17-AAG, Afungin, Trichostatin A) are displayed, showing that it also has effect in spheroidal models in the concentration range studied.
Systemic mRNA gene expression analysis
We performed systemic micoarray mRNA gene expression analysis of the changes induced by the combination (17-AAG, Afungin, Trichostatin A) in HCT116 cells to gain more insights about its mechanism of action. Induced changes in mRNA signatures for the combination as well as its constituent drugs were derived from the fold change in expression relative to vehicle control in HCT116 cells while following the Connectivity Map (CMap) protocol21. Table 3 shows the top ten most similar compounds in terms of mRNA expression signature produced by a search against the publicly available CMap database. The pattern clearly suggests the mode of action is proteotoxic, specifically inhibition of HSP90, with all top 5 hits having been described as HSP90 inhibitors22,23,24,25,26. Since 17-AAG (denoted as Tanespimycin in CMap) is part of the combination and known to be a HSP90 inhibitor and since HSP90 inhibitors are enriched in analysis, we propose that the main mechanism of actions is protetoxicity mediated through HSP90-inhibition. In this context one should also note that Trichostatin A is an indirect HSP90 inhibitor because its inhibition of HDAC627 leads to HSP90 deactivation28. Inhibition of HDAC6 also means that cells fail to clear misfolded protein aggregates from the cytoplasm, cannot form aggresomes properly and are hypersensitive to the accumulation of misfolded proteins28,29.
For more details regarding the gene expression analysis, see Supplementary Methods Part I. Using the mRNA gene expression signatures obtained, additional bioinformatics searches were performed using commercial tools like MetaCoreTM (www.thomsonreuters.com) and Nextbio (www.nextbio.com) as well as open access alternatives like Gene set enrichment analysis (www.broadinstitute.org), gene ontology (www.geneontology.org) and g:Profiler30,31. However, no additional outstanding conclusions were made.
The closest match is Withaferin A (WA) which recently was reported by Koduru et al. to inhibit cell viability in three CRC cell lines (HCT116, SW480 and SW620) in a dose-dependent manner while at the same time not having any significant effect on normal colon epithelial cells (FHC)32. Thus WA and the combination (17-AAG, Afungin, Trichostatin A) show strikingly similar phenotypic effects in the context of CRC cell lines and normal colon cell lines. However, instead of HSP90-inhibition, Koduru et al. suggest and offer experimental results supporting that WA inhibits Notch-mediated prosurvival signaling that facilitates c-Jun-NH2-kinase mediated apoptosis in colon cancer cell lines.
As discussed in the review by Vanden Berghe et al. the heat shock regulating activity of WA is still very unclear as WA has been reported to inhibit heat shock protein activity and also found to be a highly potent heat shock response inducer in screen covering 80000 natural and synthetic compounds. The authors suggest that this might be a consequence of concentration of WA applied as well as the cellular context. For example, the induction of heat shock response by WA might be secondary to WA-mediated HSP90-inhibition. WA is an unusually difficult compound to grasp as it has been reported to exert anti-inflammatory, pro-apoptotic, pro-autophagic as well as anti-invasive and anti-angiogenic effects. It has also been shown to have a remarkably wide range of molecular/cellular targets including vimentin, Bcl-2, the proteasome, NFκB, Akt, Stat3, kinase activity, notch signalling, endoplasmic recticulum stress, reactive oxygen species (ROS) production and heat shock response activity33,34. Of particular interest in this context is the reported HSP90 inhibitor activity of WA in pancreatic carcinoma cells22 and breast cancer cells35 and improved mechanistic understanding regarding this effect33,36.
As indicated in the introduction, the space of drug combinations beyond pairs of drugs has outstanding potential but is almost completely unexplored using systematic approaches. Since the wet laboratory work grows exponentially when exploring this space systematically, semi-automation seems to be the only feasible way forward. There are many multi-disciplinary challenges and pitfalls towards obtaining successful use of semi-automated procedures that are able to speed up the search for clinically promising drug combinations of arbitrary size. Taken together, the contributions presented here not only demonstrate the potential of this semi-automated approach but also provide a set of promising combinations that deserve further characterisation as candidates for cancer treatment, notably CRC. More specifically, the main contributions may be briefly summarised as follows: (1) Development and deployment of a novel semi-automated and successful computational-experimental pipeline for combination studies. (2) An independent validation of one of the first among very few search methods reported for drug combinations of arbitrary size (MACS) and clinically and practically important improvements of this approach. (3) The proposed use of two innovative in vitro model systems suitable for drug as well as drug combination screening for positive TI (pairs of cell lines having the same genetic background and multiple cell line models of cancer and normal/reference/healthy patient samples). (4) Discovery and characterisation of several drug combinations for CRC treatment showing promising activity in an extended panel of cell line models, in a 3D spheroidal model and in primary cultures of patient CRC cells.
There are multiple reasons for combination therapies. As also mentioned in the introduction, combination therapies are receiving increased attention and there are multiple reasons for this. Often the goal is to find a combination that displays synergy in the sense that the combination shows greater effect than expected from the effects of the constituent drugs. Economically, combinations are promising in the context of drug repurposing as a combination of approved drugs may target diseases for which the constituent drugs are not registered or may offer a much cheaper alternative than those currently used in the clinic. The time for a combination consisting of already FDA (Food and Drug Administration) approved drugs to reach the market is much shorter than for a novel drug candidate, since the constituent drugs have already passed clinical trials. Another commonly cited motivation for combinations is the complexity of the interacting network causing many diseases, prominently cancer. That is, combinations seem or are claimed to be needed to achieve therapeutic effects, since a single targeted drug is insufficient to target diseases driven by complex networks.
This work presents a generic framework for discovering anti-cancer drug combinations. Except for clear cut examples such as when an individually inactive drug increases the effect of the combination, synergy is a non-trivial concept to define. In addition, classical definitions of drug synergy do not correspond to clinical reality as clinically used combination therapies often display limited or no synergistic effects when investigated using in vitro models. We postulate that the clinical value of combination therapies for cancer may derive from being able to increase the total drug exposure and/or from the potency to rewire complex networks while maintaining side-effects at an acceptable level. Systematic search for promising combination therapies has conventionally been limited to consider combinations of only two drugs, where typically a potential synergistic partner for an investigational drug is evaluated. Here we have presented a framework that allows searching for combinations of a potentially arbitrary number of drugs.
In connection to the results presented, there are some algorithmic issues to consider. The TACS algorithm as presented is limited by the number of one-off (one drug away) neighbouring combinations to evaluate in each generation. However, we do not think the exact details of the optimisation algorithm are crucial. Also, we used fixed concentrations when searching for combinations. What we do think is crucial though is to take experimental variability into account as to avoid jumping around randomly among a set of combinations equally potent according to the estimated performance. Moreover, although the search space in our main example consisted of just 57 = 26 − 7 possible combinations of 2 or more drugs, our semi-automatic pipeline allows for much larger search spaces. The main limitation on the size of the library used is the ability to exhaustively evaluate all nearest (one modification away) combination neighbours in the iteration. Therefore, in practice the TACS algorithm seems most suitable for finding combination therapies from relatively small (<50) sets of compounds. For larger sets, alternative, less-exhaustive search strategies are required, which is a topic for future work.
The selection of a drug set for the TACS algorithm can be made in a variety of ways. For exploratory (de novo) studies and when there is no obvious prior knowledge to exploit, drugs can be selected more or less randomly without any prior hypothesis about their mechanism of action. However, the selection can also be based on a hypothetical model of the pathology in combination with detailed knowledge about the targets/mechanisms of particular drugs. For example one may select a set of drugs for specific targeting of one particular signal transduction pathway or biological process. In summary, since TACS is a generic combination search algorithm, the drug set used can be tailored to the particular needs of the study of interest.
The current implementation of TACS uses fixed doses of the selected set of drugs. However, it is possible to use the same drug at multiple concentrations using TACS simply by interpreting each concentration as a different drug in the TACS implementation. Additionally, if a combination is producing a large value of TI at a fixed concentration this does not directly ensure the presence of a TW as well. Therefore, one should perform validation studies to find out the existence of large TWs.
A few aspects of the clinical relevance of the presented approach and results are interesting to note. When characterizing the concentration-response surface of the combinations discovered, we find positive TI values for a range of concentrations making administration promising. Clinical use would be nearly impossible if the constituent drugs all have narrow TWs. Of course, the choice of normal (or reference/toxicity) cell models used in the iterative search to a large extent determines the possibilities to find clinically relevant combinations. The use of CCRF-CEM, a T-cell lymphoblast cell line established from an acute lymphocytic leukemia as a normal/reference/toxicity cell model is a potential weakness. However it does show generally higher chemosensitivity compared to cell lines derived from solid tumours like CRC. Sensitivity of the CCRF-CEM can also be verified from the National Cancer Institute NCI-60 DTP human tumour cell line screen database. More generally, hematologic toxicity is well known to be one of the main dose-limiting factors in clinical practice. Therefore, it may be viewed as a general marker of non-specific cytoxicity that should be avoided. We believe this interpretation and use of CCRF-CEM is strengthened by us subsequently finding limited therapeutic effects also in the normal (non-cancerous) cell line CCD 841 CoN. Lastly, it is encouraging to conclude that the combinations offer therapeutic synergy, i.e., the therapeutic benefit cannot be achieved using any of the constituent drugs on their own. Applicability of the overall iterative search strategy is further strengthened by finding a combination to have activity in CRC patient primary cell cultures within the range of, comparatively very low, concentrations explored.
The combination was also tested in tumour cell samples from patients with ovarian cancer (n = 9), kidney cancer (n = 6) and lymphoma (n = 1). From the clinic these tumour types are expected to show considerable differences in drug sensitivity, with lymphoma being sensitive, ovarian cancer intermediate and renal cancer very resistant. Interestingly, the activity of the combination was essentially equal in these diagnoses, indicating it is targeting a general mechanism in cancer cells (data not shown). Furthermore, the combination was active at relatively low concentrations of each component compared with standard drugs and without much concentration dependence within the combination. This indicates high potency of the combination with early saturation of the target mechanism. However, it is not possible on the basis of our relatively few observations to draw any strong conclusions regarding the activity of the combination in tumour samples from patients. Finally, the clinical potential of the combination is also supported by preliminary results suggesting that the combination induces cytotoxicity in a spheroid model.
One of the potential weaknesses of the current study is that in vitro measurements have limited clinical relevance37,38. Therefore, how combinations will behave in patients (clinical trials) is a question for further studies. Obviously the current study would also benefit from the use of additional in vitro non-cancer and cancer models both during the search phase and the follow up characterisation of the most promising combinations found (where results from in vivo models also would be of great interest). However this is beyond the scope of the present paper being focused on demonstrating the general potential of the approach suggested (i.e. to take experimental variability into account when employing the semi-automated search pipeline developed). Moreover, regarding the suggested hill climbing algorithm introduced (TACS) there are obvious possibilities for further algorithmic improvements that may result in even more robust and/or faster search. For example, in future studies it would be interesting to compare this type of local search methods with global optimisation methods including genetic algorithms. Moreover, it could prove beneficial to explore the possibilities to enhance the search performance by integrating prior knowledge about the drug combination search space as well as about the experimental variability associated with the experiments performed. Furthermore, in this context we would also like to make a reminder that the whole idea of searching for promising drug combinations beyond pairs of drugs often is considered as a weakness (for various reasons including potential difficulties reaching the clinic). However, as already discussed above, the potential of drug combinations beyond pairs of drugs is largely unexplored and deserves further preclinical evaluation. In this effort, new algorithms of the kind suggested and explored here will be required.
The mechanism of action of our example combination (17-AAG, Afungin, Trichostatin A) is clearly suggested to be HSP90-inhibition. It seems as if Trichostatin A and Afungin potentiate the effect, but especially the role of Afungin is unclear. We performed additional analyses of the combination induced mRNA expression changes, sifting out the set of probes perturbed uniquely by the combination. However, using various bioinformatics tools for pathway analysis (see above) no outstanding pathway or function could be discerned among the annotations. One should also note that the closest compound matching when performing a CMap based systemic mRNA analysis was Withaferin A (WA) which recently was reported by Koduru et al. to inhibit cell viability in three CRC cell lines (HCT116, SW480 and SW620) while at the same time not having any significant effect on normal colon epithelial cells (FHC)32. The same report also suggests that WA achieves its effect via inhibition of Notch-mediated prosurvival signaling, thus not via HSP90-inhibition. Further investigations into the mechanism of the combination are ongoing.
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This work was supported by the Higher Education Commission of Pakistan (MK) as well as by the SSF (Swedish Foundation for Strategic Research) framework project “Tools for diagnosis and drug discovery in cancer” (CA, SH, MK). The SSF project was also providing the iso-genic cell lines used in this project which were made available to us via our SSF project collaborators Tobias Sjöblom and Tatjana Djureinovic at the Department of Immunology, Genetics and Pathology, Uppsala University. Many thanks also to Christina Leek, Lena Lenhammar and Nasrin Najafi for skillful help in the wetlab part of the project and to Wesley Schaal at the Department of Pharmaceutical Biosciences, Uppsala University, for English language advice. Financial support: This work was supported by the Higher Education Commission of Pakistan (MK) as well as by the SSF (Swedish Foundation for Strategic Research) framework project “Tools for diagnosis and drug discovery in cancer” (CA, SH, MK).
The authors declare no competing financial interests.
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Kashif, M., Andersson, C., Hassan, S. et al. In vitro discovery of promising anti-cancer drug combinations using iterative maximisation of a therapeutic index. Sci Rep 5, 14118 (2015). https://doi.org/10.1038/srep14118
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