- Methodology article
- Open Access
Prediction of kinase inhibitor response using activity profiling, in vitro screening, and elastic net regression
© Tran et al.; licensee BioMed Central Ltd. 2014
- Received: 30 April 2014
- Accepted: 18 June 2014
- Published: 25 June 2014
Many kinase inhibitors have been approved as cancer therapies. Recently, libraries of kinase inhibitors have been extensively profiled, thus providing a map of the strength of action of each compound on a large number of its targets. These profiled libraries define drug-kinase networks that can predict the effectiveness of untested drugs and elucidate the roles of specific kinases in different cellular systems. Predictions of drug effectiveness based on a comprehensive network model of cellular signalling are difficult, due to our partial knowledge of the complex biological processes downstream of the targeted kinases.
We have developed the Kinase Inhibitors Elastic Net (KIEN) method, which integrates information contained in drug-kinase networks with in vitro screening. The method uses the in vitro cell response of single drugs and drug pair combinations as a training set to build linear and nonlinear regression models. Besides predicting the effectiveness of untested drugs, the KIEN method identifies sets of kinases that are statistically associated to drug sensitivity in a given cell line. We compared different versions of the method, which is based on a regression technique known as elastic net. Data from two-drug combinations led to predictive models, and we found that predictivity can be improved by applying logarithmic transformation to the data. The method was applied to the A549 lung cancer cell line, and we identified specific kinases known to have an important role in this type of cancer (TGFBR2, EGFR, PHKG1 and CDK4). A pathway enrichment analysis of the set of kinases identified by the method showed that axon guidance, activation of Rac, and semaphorin interactions pathways are associated to a selective response to therapeutic intervention in this cell line.
We have proposed an integrated experimental and computational methodology, called KIEN, that identifies the role of specific kinases in the drug response of a given cell line. The method will facilitate the design of new kinase inhibitors and the development of therapeutic interventions with combinations of many inhibitors.
- Drug response predictions
- Kinase inhibitors
- Elastic net regression
- High throughput screening
- Drug combination therapies
The important role of kinases in cancer biology  has spurred a considerable effort towards the synthesis of libraries of fully profiled kinase inhibitors, providing a map of the strength of each compound on a large number of its potential targets [2–4]. In particular, a recently published dataset has profiled several hundred kinase inhibitors using a panel of more than 300 kinases . These profiled libraries define a network of interactions between drugs and their kinase targets , and represent a valuable resource for the development of new therapies. In this paper, we introduce a novel computational method that incorporates profiled libraries and in vitro measurements to predict the response of cells to previously untested drugs. Besides making prediction about the cellular response to drugs, the method identifies critical kinase targets and pathways that are statistically associated to drug sensitivity in a given cell line.
Statistical inference and regression methods in conjunction with gene expression or mutations have been used to identify specific biomarkers associated with an increased sensitivity/resistance to drugs. For instance, the sensitivity to PARP inhibitors of Ewing’s sarcoma cells with mutations in the EWS gene and to MEK inhibitors in NRAS-mutant cell lines with AHR expression have been predicted using analysis of variance and the elastic net method  and then experimentally validated [7, 8]. In these analyses, the statistical variable associated to drugs was represented by the half maximal inhibitory concentration (IC50) in different cell lines. However, besides the IC50, there are many other types of information that characterize chemical compounds. These types of information can enhance the statistical analyses and improve the accuracy of predictions. For instance, a method to predict drugs sensitivity in cell lines based on the integration of genomic data with molecular physico-chemical descriptors of the drugs has been recently proposed . Another useful type of information is the residual activity of kinases after interacting with a compound. Kinase profiling, patient genetic profiles, and sensitivity of primary leukemia patient samples to kinase inhibitors were recently used by Tyner et al. to identify functionally important kinase targets and clarify kinase pathway dependence in cancer.
In this paper, the residual activity of kinases upon drug interaction is used to make predictions of the cellular response for in vitro experiments using an elastic net  regression approach. This regression method reduces the number of predictors to a minimum set, providing a clear picture of the kinases involved in the response of cell lines. A primary screen (single drug) and a secondary screen (two-drug combinations) are used as the training set for the regression. The two-drug screening exhibits a broader distribution in the response and provides a good level of predictability. In fact, the model based only on single drug response did not pass the statistical cross-validation test.
We are applying this Kinase Inhibitor Elastic Net (KIEN) method to predict cell viability of a lung cancer cell line (A549) and a normal fibroblast cell line (IMR-90) after drug treatment. We found that the regression can be improved through a logarithmic transformation on the data. Using the results of the regression, we identified a set of kinases that are strongly associated to a selective response of A549 and not IMR-90. Then, a pathway-based enrichment using Reactome  revealed ten significant pathways using this set of kinases, including axonal guidance and related semaphorin interactions as top hits.
This paper is organized as follows: Section In vitro screen of the kinase inhibitor library contains the experimental results of the primary and secondary in vitro screening corresponding to single drugs and two-drug combinations. These experimental results and residual kinase activity are analyzed with Pearson’s correlation in Section Analysis of correlations. This simple correlation analysis gives a first glance of the kinases that are statistically associated to a significant change in the viability of cancer and normal cell lines. In Section Elastic net regression, we introduce the elastic net approach and we present the results of a leave-one-out cross validation for predictions on single and pairs of drugs. We also present in this section the results obtained using the logarithmic transformation on the variables and a pathway enrichment analysis using Reactome . The Discussion of the results is in Section Discussion, conclusions in Section Conclusions, and Materials and Methods in Section Materials and methods.
In vitro screen of the kinase inhibitor library
Analysis of correlations
In our second step, we analyzed the Pearson’s correlation of the primary and secondary screening with a published dataset  containing target profiles for 140 kinase inhibitors. Therefore, even though we had a library of 244 KIs in the experimental screening, we were limited to utilizing 140 KIs for the analysis. For each inhibitor, the dataset provides the residual activity (0 ≤ A ≤ 1) of 291 kinases after drug treatment. This quantity is a measure of the strength of inhibition of a drug on each kinase.
Correlations between selectivity and kinase activity from primary and secondary screening
Elastic net regression
A fitting procedure based on a training set of measurements produces the coefficients (β 0, β 1, …, β p ). Equation (1) can then be used to predict the viability of a new drug that has not been tested, but of which the profiling information is available. Note that we are integrating two different types of data: kinase profiling data is obtained through enzymatic assays that probe directly the interaction between drug and kinases, while the in vitro cell response data is the result of complex signaling that involves many pathways downstream of the affected kinases. The coefficients β k can be seen as a measure of the sensitivity of a given cell line due to alterations in the activity of kinase k.
It is well known that the least square method does not perform well in the case of linear regression with many predictors. In our case, we would like to use a database of drugs that have been profiled on about 300 kinases. However, it would be desirable to select and keep in the final model a minimal set of the kinases that provide a simple model, useful to gain biological insight. The lasso technique  is a powerful method to reduce the number of predictors by imposing a penalty on the regression coefficients. However, in the presence of a group of kinase predictors with strong mutual correlation, the lasso could select only one kinase predictor from the group while missing the others. To prevent this problem, our method uses the elastic net approach. This method incorporates the lasso penalty as well as a ridge penalty to keep the regression coefficients small without completely removing them . The weights of the ridge and lasso penalties in the least square procedure can be optimized for best performance of the method.
Kinases with the highest difference in the regression coefficients for the log transformed data of the secondary screen
Cancer beta coefficient
Normal beta coefficient
Reactome pathways with significant representation of kinases from the regression analysis
Activation of Rac
Signaling by Robo receptor
Signal transduction by L1
p75NTR signals via NF-kB
p75NTR recruits signaling complexes
CD28 dependent Vav1 pathway
Drug-kinase profiling represents a controller-target network  that when combined with in vitro testing, can be used in regression models to predict drug response and to identify pathways statistically associated to drug sensitivity. Network methods in biology are often based on the analysis of large datasets from high-throughput experiments. An example is given by gene regulatory networks, which presents many challenges either when restricted to a homogeneous set of data [15, 16] or when it includes different classes of data [17–20]. In our KIEN method, information from the drug-target network and experimental query of the biological system are integrated. The goal is not a reconstruction of a regulatory network, but to identify a set of kinases linked to a therapeutic response in a given cell line. In order to establish associations, the system has to be perturbed by the use of kinase inhibitor drugs. The response to these single drugs or drug combinations becomes a training set that when combined with the kinase profiling, can lead to predictions.
The elastic net method is one of the most widely used regularization techniques. Regularization techniques are used in statistical and machine learning models to achieve an optimal tradeoff between accuracy and simplicity. Simplicity makes a model less prone to overfitting and more likely to generalize. In our analysis, we found that the elastic net regressions based on single drug responses were not successful, while drug pair data provided statistically significant predictions. A possible explanation for this finding is the following: single drugs might be less able to overcome the robustness of biological networks . The phenotypic signal is therefore blunted and not easily measured. If a second drug is added, any compensatory capacity is already stretched and the effects from the inhibition of each kinase can be seen more clearly. Using data from drug pairs, we found that noise can be better filtered out and stronger statistical associations between kinases and therapeutic response are revealed. Clearly, if a different training set with higher variance in efficacy measures were used in the primary screen, it is likely that also single drug in vitro response would have given a significant predictive model.
We identified several kinases that are implicated in lung cancer that gives biological significance to our KIEN method. In particular, TGFBR2 appears as a top hit both in the correlation and in the elastic net methods. This finding is consistent with recent siRNA experiments on A549 cell lines , which demonstrated that silencing of this receptor reduces cell proliferation, invasion, and metastasis. The Cyclin-dependent kinase 4 (CDK4) appears as a second top target in the correlation analysis, and is also highly significant in the KIEN analysis. Experiments using lentiviral-mediated shRNA to inhibit CDK4 in A549 have shown inhibited cell cycle progression, suppressed cell proliferation, colony formation, and migration , and there is an ongoing clinical trial using a CDK4/6 inhibitor in lung cancer . The KIEN analysis identified EGFR, which is known to be overexpressed in the majority of non-small cell lung cancers . Furthermore, RNAi experiments targeting EGFR demonstrated cancer growth suppression in A549 xenograft in mice . The third kinase in Table 2, PHKG1 has also been found to be upregulated in human tumor samples, including lung adenocarcinoma, and aberrations in its gene copy number is a feature of many human tumors .
The pathway-based enrichment provides a broader view on the role of the kinases identified by our method in Table 2. Among the top three pathways shown in Table 3 are activation of Rac and Semaphorin interactions. Rac proteins play a key role in cancer signaling and they belong to the RAS superfamily . We also identified a set of semaphorins in our analysis that is represented in the top significantly enriched pathways. Semaphorins, previously known as collapsins, are a set of proteins containing a 500-amino acid sema domain among others (including PSI and immunoglobulin type domains), which can be transmembranous or secreted . It is known that Sema3E cleavage promotes invasive growth and metastasis in vivo. These genes also have selective targeting by Rac and Rho family members. This generates hypotheses of possible pathways that could be targeted therapeutically. However, these hypotheses need to be validated by further experiments with different inhibitors for the same targets or with alternative methods, e.g. using siRNA.
We have introduced an integrated experimental and computational methodology that identifies the role of specific kinases in the drug response of a given cell line. The key element of our KIEN methodology is a multiple regression procedure that uses in vitro screen data as a training set. If a new library of kinase inhibitor compounds were to be synthetized and profiled, then our model would be able to immediately estimate the effect of these drugs on in vitro experiments on a given cell line. We have shown an application to a lung cancer cell line, but our method can be extended to different cell lines. The method will facilitate the design of new kinase inhibitors and the development of therapeutic interventions with combinations of many inhibitors . The procedure could be extended to three drug combinations, if measurements for these larger combinations were available. Finally, the method could be extended to regression models that are specific of cancer cells with the same set of mutations, or it could be directly used with patient-derived primary cells to identify a personalized treatment.
The primary screening of a kinase inhibitor (KI) library comprised of 244 KIs was purchased from EMD Chemicals, and diluted with DMSO to 2 mM concentrations for high-throughput screening purposes. The KI library was stored at -80°C. Additionally, PDK1/Akt1/Flt3 Dual Pathway Inhibitor (CAS # 331253-86-2) was ordered from EMD. Only 140 out of 244 were used in the drug-target network reconstruction because the drug profiling information was available only for these compounds. One kinase inhibitor known to affect the kinase targets indirectly was excluded. We provide in Additional file 2 the chemical structure of kinase inhibitors with highest selectivity in the primary and secondary screening.
Cell lines IMR-90 (normal lung fibroblast) and A549 (lung adenocarcinoma) were cultured in RPMI 1640 (Hyclone) supplemented with 10% Canadian characterized fetal bovine serum (Hyclone), 1% 200 mM L-glutamine (Omega), and 1% penicillin/streptomycin (Omega). The media for the cells were renewed every 3 days and kept at 80-90% confluency. Cells were maintained in a humidified environment at 37°C and 5% CO2.
Kinase inhibitor experiments
IMR-90 (1500 cells/well) and A549 (750 cells/well) were seeded on 384-well microplates (Grenier Bio-One) and incubated for 3 hours before the addition of kinase inhibitor(s). The reason that IMR-90 was seeded at double the cell density of A549 is due to the difference in cell division. IMR-90’s doubling time is 36–48 hours whereas A549’s is 22 hours. We wanted to make sure that the cells have divided at least once during the 72 hr drug treatment. Furthermore, both A549’s and IMR-90’s final confluency at 72 hrs is 90-95% and within the range of the ATPlite 1step assay. Additional file 1: Figures S1 and S2 show the growth curve for both cell lines. IMR-90 and A549 cell lines were tested on the same day with three replicates and the experiment was repeated three times with randomized well positions to reduce biases. ECHO 555 Liquid Handler (Labcyte) was used to dispense nanoliter volumes of each KI to 384-well plates with cells attached (wet dispense). The final volume in the plate is 40uL and cells were incubated for 72 hours with KI treatment.
ATPlite 1Step (Perkin Elmer) was used to evaluate the cell number and cytotoxicity. ATP measurements were done by dispensing 20 uL of the ATPlite 1Step solution to each well to a final volume of 60 uL. The plate was placed on a shaker at 1100 rpm and the luminescence activity was detected by Analyst GT Plate Reader. The percent (%) of control is the quantity of ATPlite 1step measurement of the treated versus the untreated wells of each individual cell type. The ATP standard was prepared with culture media to final volume of 40 uL, and 20 uL of ATPlite 1step reagent was added. Additional file 1: Figure S3 shows the ATP standard curve. The plate was read immediately.
where v is the vector of the observed viabilities and A is the matrix containing the residual activity of the kinases from the profiling, and M is the total number of drugs or drug combinations used. The parameters α and β determine the relative weights of the lasso and ridge penalties quantified using L 1 (|| |1 ) and L 2 (|| ||2) norm, respectively. We used α = 0.15 and ρ = 0.01 in the results of Figures 4 and 5 and in Table 2. We also tried other values of these parameters, which did not give a significant difference in the results.
Reactome pathways were downloaded using a newer build of the 'biomaRt’ library (v2.12.0) in Bioconductor/R (v2.15.0). Gene symbols from the kinase list were converted to Entrez gene identifier numbers ('entrezgene’) and mapped against the gene ids in each Reactome pathway. For each pathway, the set of significant genes enriched within any given pathway was computed using a Fisher exact test. The procedure computes the significance (p-value) of observing significant kinases, as deemed significant by our method, within the selected pathway. These pathways are identified from 518 Reactome pathways. Given that our gene set consists entirely of kinases and would be generalized towards kinase-specific effects, the set of all kinases (~300) were selected for background adjustment and more sensitive enrichment of the pathways. This procedure was repeated for each pathway to generate p-values and pathway rankings. False discovery rate [FDR] values were later generated to further restrict significance.
We thank Dr. Anthony (Tony) Polverino for many discussions. We would like to acknowledge the NSF grant (CCF0829891) and the DOD/CDMRP Lung Cancer Research Program (grant W81XWH-12-1-0233) for support.
The data sets supporting the results of this article are included within the article. Correspondence and requests for materials should be addressed to email@example.com or firstname.lastname@example.org.
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