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# The drug cocktail network

*BMC Systems Biology*
**volume 6**, Article number: S5 (2012)

## Abstract

### Background

Combination of different agents is widely used in clinic to combat complex diseases with improved therapy and reduced side effects. However, the identification of effective drug combinations remains a challenging task due to the huge number of possible combinations among candidate drugs that makes it impractical to screen putative combinations.

### Results

In this work, we construct a 'drug cocktail network' using all the known effective drug combinations extracted from the Drug Combination Database (DCDB), and propose a network-based approach to investigate drug combinations. Our results show that the agents in an effective combination tend to have more similar therapeutic effects and share more interaction partners. Based on our observations, we further develop a statistical approach termed as DCPred (__D__ rug __C__ ombination __Pred__ ictor) to predict possible drug combinations by exploiting the topological features of the drug cocktail network. Validating on the known drug combinations, DCPred achieves the overall AUC (Area Under the receiver operating characteristic Curve) score of 0.92, indicating the predictive power of our proposed approach.

### Conclusions

The drug cocktail network constructed in this work provides useful insights into the underlying rules of effective drug combinations and offer important clues to accelerate the future discovery of new drug combinations.

## Background

Drug combination is the combination of different agents that can achieve better efficacy with less side effects compared to its single components. Recently, it is becoming a popular and promising strategy to new drug discovery, especially for treating complex diseases, e.g. cancer [1–3]. For example, Moduretic is the combination of Amiloride and Hydrochlorothiazide, which is an approved combination used to treat patients with hypertension [4, 5]. Chan *et al.* identified a combination drug, namely Tri-Luma, for combating melasma (dark skin patches) of the face based on efficacy and safety experiments [6]. Agrawal *et al.* found two effective combinatorial drug regimens to treat Huntington disease based on prescreening in *Drosophila* [7]. In addition, through the synergistic antiangiogenic effects, very low-dose combinatorial use of vinblastine (VBL) and rapamycin (RAP) was demonstrated to inhibit the proliferation of the endothelial cells much more effectively than single drug treatment both *in vitro* and *in vivo* [8]. Recently, Lehar *et al.* found that synergistic drug combinations may have less side effects, because synergistic drug combinations are generally more selective to particular cellular contexts than single agents, and the dosage of each compound in combination will be reduced comparatively [9]. Despite of the extensive efforts that have been made to discover new drug combinations in the past few decades, the majority of effective combinatorial drugs used in clinic were discovered through experiences, which generally require labor-intensive and time-consuming "brute force" screening of all possible combinations among the approved individual drugs [10]. In a drug combination, a drug may promote or suppress the effect of another one. For instance, cyclosporine increases the effect of sirolimus, while bupropion decreases the effect of cyclosporine. As a result, two drugs may have a totally new effect that is different from the ones of either individual drugs [11, 12]. Accordingly, the presence of potential drug-drug interactions (DDIs) and the possibility of pharmacokinetic interventions between the drugs could confound the identification of effective drug combinations [13]. Furthermore, the number of possible combinations will increase exponentially with the increasing availability of single drugs. For example, in the case of four drugs, there will be six possible combinations. This number would be enormous considering the fact that there are thousands of approved drugs. Due to the huge search space of possible combinations between known drugs, the identification of optimal and effective drug combinations is a non-trivial and challenging task.

Therefore, it is necessary to develop effective *in silico* methods that are capable of discovering new drug combinations prior to combination synthesis and practical test in the lab. Owing to the completion of human genome sequencing projects and the advancement of molecular medicine, extensive system biology efforts have been made to discover new combinations based on molecular interaction networks [14, 15] in the past few years [16–19]. Nevertheless, there is still a long way to go before we reach the stage of devising generally applicable and effective prediction models. Recently, there have been considerable progresses in developing new approaches for identifying drug-drug interactions and even drug combinations [13]. In this context, Geva-Zatorsky *et al.* have recently found that the protein dynamics in response to drug combination can be accurately described by a linear superposition of the dynamics under the corresponding individual drugs [16]. Their study indicated that protein dynamics of three- and four-drug combinations can be predicted based on the drug combination pairs, thereby providing a useful way for reducing the search space of possible drug combinations. Calzolari *et al.* devised an efficient search algorithm originated from information theory for optimization of drug combinations based on the sequential decoding algorithms [17]. More recently, researchers have also developed computational frameworks for predicting drug combinations and synergistic effects based on high-throughput data [18–20].

In this work, we study the drug combinations in terms of their therapeutic similarity and the network topology of a drug cocktail network constructed from the effective drug combinations deposited in the Drug Combination Database (DCDB) [21]. We find that the drugs in an effective combination tend to have more similar therapeutic effects and share more interaction partners in the context of drug cocktail network. We further develop a statistical approach called DCPred to predict possible drug combinations and validate this approach based on a benchmark dataset with all the known effective drug combinations. As a result, DCPred achieves the overall best AUC (Area Under the receiver operating characteristic Curve) score of 0.92, demonstrating the predictive capability of the proposed approach and its potential value in identifying new possible drug combinations.

## Results and discussion

### The drug cocktail network

In this study, we extracted 239 known effective pairwise drug combinations from DCDB [21]. The information of ATC code for each drug was obtained from DrugBank [22]. Based on these datasets, we constructed a drug cocktail network with 215 nodes and 239 edges (see Figure 1 for the visualization of this network), where nodes represent the drugs and an edge is connected if two drugs are found in an effective drug combination. Building up this network can thus give the readers a visual impression of the relationships between drugs that can form effective combinations. Moreover, the network theory can be utilized to explore possible combinatorial mechanisms between drugs. In Figure 1, the size of each node approximates its degree, and the width of each edge approximates the therapeutic similarity (*TS*) (as defined in Equation 3) between the two drugs linked by the edge, while the grey edges indicate that the two drugs linked by the edge have totally different therapeutical effects. In addition, we found 102 drugs that have at least two neighbors in the drug cocktail network, which we termed as "star drugs" hereafter and 91 of which have target protein annotations in DrugBank.

Since most of biological networks are scale-free networks [23], we analyzed the topology of the drug cocktail network in order to find out whether it is also a scale-free network. The degree distribution of the drug cocktail network is shown in Figure 2. It is evident that the degree distribution follows a power law distribution, suggesting that it is indeed a scale-free network. That is, the fraction *P(x)* of nodes in the drug cocktail network having *x* connections to other nodes can be described as:

where *c* = 2.1 and *α* = 1.9 in this case.

As the drug cocktail network shown in Figure 1 is not fully connected, the top 6 largest subnetworks were chosen for further analysis. We considered the drug cocktail network as the union of these 6 subnetworks hereafter unless stated specifically. In particular, each subnetwork was found to be enriched for one or several therapeutic classes according to the ATC classification system, as shown in Table 1. In other words, the drugs having similar therapeutic effects tend to be clustered together in the drug cocktail network.

To test our hypothesis that the drugs in one combination tend to have similar therapeutic effects, the drug cocktail network was compared against random combination networks. For this purpose, a therapeutic similarity (*TS*) score was calculated for each drug pair, and the average of all *TS* scores was used as the *TS* score for the whole drug cocktail network. The random combination networks were generated by randomly shuffling the edges while still preserving the degree for each node [24] in the drug cocktail network. This procedure was repeated for 1,000 times. To examine the statistical significance of the difference between the drug cocktail network and random combination networks, one *P*-value was calculated as the ratio that the *TSs* of random combination networks are larger than that of the drug cocktail network during the 1000 randomizations. The results are shown in Table 2 at different ATC code levels ranging from 1 to 4. The calculated *P*-values of the drug cocktail network across ATC code levels 1-4 are all equal to 0, strongly suggesting that the real drug combinations significantly differ from the random combination networks. Note that the 5^{th} ATC code level was not considered here, as there is only one drug combination having identical ATC codes for all the five levels in the drug cocktail network. This means that the 5^{th} ATC code level is not suitable for performing statistical analysis and thus it is not included in the analysis.

Furthermore, we studied the therapeutic effects for the "star drugs" and their neighbors in the drug cocktail network in order to reveal whether the star drugs have therapeutic similarities to all their neighbors. Figure 3 shows the distribution of the *TS* scores for star drugs and their neighbors. For the effective combination pairs involving star drugs, 82% have therapeutic similarity, and most of the star drugs have similar therapeutic effects as the majority of their neighbors. In contrast, 78% of the combination pairs in the random network do not have any therapeutic similarity. These results suggest that one star drug tends to be used in combination with drugs that have similar therapeutic effects as the star drug.

Moreover, we also investigated the distribution of neighbor drug pairs of star drugs (Figure 4A and 4B), attempting to answer whether or not the drug pairs that share a star drug have therapeutic similarity. To address this, we divided the neighbor drug pairs of a star drug into two groups, according to whether they have similar ATC codes, or whether they are approved effective combinations. We then calculated the percentage of effective combinations among drug pairs that share a star drug and have a *TS* score equal to or larger than a certain threshold (Figure 4C). From Figure 4C, we can see that the more similar therapeutic effects (as reflected by the *TS* score) two drugs have, the more likely they are effective combinations. Another important observation is that the combinations between drugs sharing similar therapeutic effects and star drugs are more likely effective combinations.

In various networks, the hub nodes are generally considered to play important roles [25]. Therefore, we next studied the 14 hub drugs in the drug cocktail network, all of which have more than 6 neighbor drugs. The largest two hub drugs are DB00999 (Hydrochlorothiazide) and DB00072 (Trastuzumab). Hydrochlorothiazide is used to treat high blood pressure and edema [26, 27]. According to the annotations in DrugBank and DCDB, we found that all the 18 drug neighbors of hydrochlorothiazide can be used to cure hypertension while all the drug combinations involving hydrochlorothiazide have been used to treat hypertension. Among these 18 combinations, 11 combinatorial drugs target different but related pathways while the other 7 ones target unrelated pathways (Additional file 1). In the case of Trastuzumab used to treat HER2-positive metatsatic breast cancer [28, 29], 5 of its 10 neighbor drugs are used to treat breast cancer, while the other 5 have pesticide effects on neoplasm or other cancers. All the 10 drug combinations are used to treat breast cancer except the one used for treating gastric cancer. Additionally, 8 drug combinations target related pathways, while the other two target different unrelated pathways or cross-talking pathways (Additional file 2). Finally, these results, together with the consistent findings shown in Figure 3, strongly indicate that star drugs tend to have similar therapeutic characteristics as their neighbors.

In addition, we investigated the proteins targeted by the 13 hub drugs in the drug cocktail network that have target information. By mapping all proteins targeted by the drugs in the drug cocktail network to the human protein-protein interaction network retrieved from STRING database [30], we found that, in terms of the shortest distance between target proteins, hub drugs tend to have a closer relationship with their combination partners than the drugs having similar ATC codes (see Figure 5A). Furthermore, we analyzed the cellular localizations of these target proteins of the 13 hub drugs(see Figure 5B). More than 70% of the target proteins of the hub drugs are membrane proteins, which is reasonable considering that membrane proteins are widely involved in various biological processes and represent the largest class of drug targets.

### Implication of drug cocktail network for possible drug combinations

As shown in Figure 3, 82% of the combinations between star drugs and their neighbors have therapeutic similarity, and most of the star drugs have therapeutic similarity to the majority of their neighbors in the drug cocktail network. Additionally, most of the effective combinations are observed to be located in the vicinity of drug pairs with similar ATC codes. Hence, it is possible to predict drug combinations from the set of drug pairs with similar ATC codes. Nonetheless, we found that there are only 74 known effective combinations in all of the 1181 possible combinations with similar ATC codes. Since the number of effective drug combinations is considerably smaller than that of random combinations between drugs having similar ATC codes, it is a challenging but crucial task to discover the effective combinations from the pool with a vast number of random combinations.

In Figure 4B and 4C, we can see that if two drugs with similar ATC codes have a common neighbor in the drug cocktail network, they are more likely to be combined together. Therefore, we assume that the two drugs having similar ATC codes and sharing a significantly larger number of common partners in the drug cocktail network are more likely to be combined effectively. Based on this assumption, we further developed a new statistical approach called DCPred to test this hypothesis and applied it to predict and rank all the possible drug combinations (See Materials and methods for more details). In particular, three different versions of DCPred were considered in this work, including DCPred1 considering *TS* only, DCPred2 considering *TS* and drugs with at least 2 neighbors, and DCPred3 considering *TS* and drugs with at least 3 neighbors. In the case of DCPred2 and DCPred3, all possible drug combinations were ranked in ascending order according to the *p*-value by equation (4), and the top ones were considered as putative effective drug combinations. While in the case of DCPred1, all possible drug combinations were ranked in descending order according to the *TS* value by equation (3), and the top ones were considered as putative effective drug combinations. The ranking list of drug combinations can be found in the additional files (Additional file 3 and 4). We found that two drugs with more common neighbors generally have higher rankings. Using the set of 74 effective combinations as the gold standard while the 1107 random ones as negative set (Additional file 3), we evaluated our approach in identifying new drug combinations. Figure 6 shows the ROC curves [31] obtained by different methods, where the drug pairs ranked above a given threshold were predicted as effective drug combinations (positives), while the rest were regarded as negatives. We then calculated the area under the ROC curves (AUC) [32] for these different DCPred models. As a result, DCPred2 achieved an AUC score of 0.88 (the green curve in Figure 6), in comparison with the AUC of 0.75 for the *TS*-based method (DCPred1) (the red curve in Figure 6). To comprehensively evaluate the predictive power of the three models, we also calculated three other performance indexes: Sensitivity, Specificity and Accuracy at varying thresholds for DCPred1, DCPred2 and DCPred3 models (See the Additional file 5, 6 and 7, respectively).

Of the top 35 ranked drug combinations inferred by our models, 63% of them (22/35) are known effective drug combinations according to DCDB, and 37% (13/35) do not have any annotations in DCDB (Table 3). Nevertheless, 4 out of these 13 drug combinations were reported in the literature, i.e. the 13^{th}, 22^{th}, 34^{th} and 35^{th} in the ranking list (Table 3). The 34^{th} ranked one is a combination of irinotecan and capecitabine, known as XELIRI, and used to treat metastatic colorectal cancer [33]. Alfonso *et al.* demonstrated that XELIRI is effective and safe as the first-line chemotherapy for treating advanced colorectal cancer or metastatic colorectal cancer [34]. The 13^{th} ranked one is the combination of docetaxel and gemcitabine, the former interferes with the normal function of microtubule growth and destroys the cell's ability to use its cytoskeleton in a flexible manner, while the latter inhibits thymidylate synthetase leading to inhibition of DNA synthesis and cell death [35, 36]. Levy *et al.* found that gemcitabine-docetaxel combination has a favorable risk-benefit profile and is an important new treatment option for women with metastatic breast cancer [37]. The 22^{th} one is the combination of sorafenib and bevacizumab. The former interacts with multiple intracellular (CRAF, BRAF and mutant BRAF) and cell surface kinases (KIT, FLT-3, VEGFR-2, VEGFR-3, and PDGFR-ß) to reduce blood flow to the tumor for the treatment of patients with advanced renal cell carcinoma [38], while the latter binds VEGF and prevents the interaction of VEGF to its receptors (Flt-1 and KDR) on the surface of endothelial cells [39]. Consequently, this prevents blood vessel proliferation and tumor metastasis for metastatic colorectal cancer and HER2-negative metastatic breast cancer. Azad *et al.* demonstrated that complementary inhibition of VEGF signaling has synergistic therapeutic effects, and this combination therapy has promising clinical activity over ovarian cancer [40]. The 35^{th} one is the combination of thalidomide and lenalidomide. Thalidomide has been successfully introduced to treat multiple myeloma and its analogue, lenalidomide, is also effective in relapsed refractory myeloma [41]. The Thalidomide-lenalidomide combination can induce tumour cell apoptosis directly or indirectly by altering bone marrow microenvironment, and can be used in combination to treat multiple myeloma [42]. Both drugs bind to a common target PTGS2, which may play a role as a major mediator of inflammation and/or a role for prostanoid signaling in activity-dependent plasticity [43]. Thalidomide and lenalidomide have been shown to significantly improve the overall and disease-free survival. Combination of these two drugs has recently emerged as a promising combination strategy to improve the patient outcome and drug toxicity, especially in the treatment of multiple myeloma (MM) and hematologic cancers [44].

If we only considered the combinations whose drug components have at least 3 neighbors, termed as DCPred3 (the blue curve in Figure 6), we predicted 40 combinations and 379 negative ones (Additional file 4). DCPred3 achieves an AUC score of 0.92. Compared with the aforementioned two models DCPred1 and DCPred2, based on the information of at least 3 neighor drugs, DCPred3 leads to the overall best performance. In this work, we considered the results by DCPred2 as the final results because only few drugs have more than two neighbors in the drug cocktail network. We hope that the DCPred models developed in this study can be used to facilitate the *in silico* identification of effective drug combinations and speed up the future discovery process.

## Conclusions

Drug combination is a promising strategy for combating complex disease, but our complete understanding of the underlying mechanisms of drug combination is largely lacking at present. It is therefore imperative to develop efficient computational methods to infer effective drug combinations in order to reduce the labor-intensive, time consuming trial-and-error experiments. In this article, we extracted all the known effective drug combinations from DCDB and constructed a drug cocktail network, which includes 215 drugs and 239 effective drug combinations. Based on this cocktail network, we observed that the star drugs tend to have therapeutic similarity with their drug neighbors, and two drugs having similar therapy and sharing neighbors tend to be employed in drug combination. Our analysis also revealed that: 1) hub drugs usually have similar and even the same therapeutic effects as their neighbors; 2) target proteins of the hub drugs are often membrane or membrane-associated proteins; 3) the components in effective drug combinations usually have more similar therapeutic effects, making the drug cocktail network significantly different from the random combination networks.

From the above observations, we consequently developed a new statistical approach to infer and rank possible effective drug combinations by taking into account drugs with at least two or three drug neighbors. As a result, our DCPred2 and DCPred3 models achieved the AUC scores of 0.88 and 0.92, respectively, demonstrating a good performance. We further applied these models to rank all the possible drug combinations and found that the top ranked combinations are more likely to be effective combinations, according to the cross-reference to the literature or the similarity of their ATC codes. In particular, four combinations in the top 35 rankings have been verified as effective combinations by the literature search. We also show that there is a better chance for another 3 combinations to be effective combinations in terms of the pharmacological similarity. Our results in this study provide useful insights into the underlying mechanisms of effective drug combinations and hence important clues for efficiently reducing the search space of possible combinations within the approved drugs. Our approach may be further useful for developing more accurate models. The DCPred models are anticipated to be applied to screen more effective drug combinations with clinical importance.

Furthermore, the concentration of each drug in a combination is a crucial factor in the study of drug combination. However, it is currently difficult to utilize the dosage information of drugs without the knowledge of their quantitative dose-response profiles (e.g. drug induced gene/protein expression data) under different drug concentrations, due to the limited availability of such data. We will investigate drug combinations from this perspective in the future, when more data regarding drug concentrations become available.

## Methods

### Data sources

The annotations of drug combinations were retrieved from a newly released Drug Combination Database (DCDB) [21]. This is a major resource for collecting effective drug combinations from the literature. The target protein information, the Anatomical Therapeutic Chemical (ATC) code annotation of the drugs and protein subcellular localizations, were extracted from DrugBank [22]. Drug combinations that do not have ATC codes for the corresponding drug components and combinations with none or unclear efficacy were discarded. Finally, 194 effective drug combinations were obtained, including 76 approved combinations, 64 clinical combinations and 54 preclinical combinations. We then split the combinations with more than two drug components into combination pairs, resulting in 239 drug combination pairs. These drug combinations were used to construct a drug cocktail network (Figure 1), where the nodes represent drugs and the edges represent combinations, respectively. In the drug cocktail network, the size of each node denotes its degree and the width of each edge denotes the therapeutic similarity (*TS*) between the two drugs linked by the edge. The gray edge means that there is no therapeutic similarity between the two drugs.

Human protein-protein interactions (PPIs) with high confidence from STRING [30] were used to annotate this drug cocktail network, which includes 169,603 interactions between 11,289 proteins after removing pairs with low scores ( < 700).

### Drug therapeutic similarity

The Anatomical Therapeutic Chemical (ATC) Classification System, which includes 5 different hierarchical levels, was used to classify drugs into different groups according to the organ they acted on and the therapeutic chemical characteristics. The *k-* th level drug therapeutic similarity (*S*_{
k
}) between two drugs is defined using the ATC codes of these two drugs:

where *ATC*_{
k
}*(d)* denotes all the ATC codes at the *k-* th level of drug *d*. Note that a drug has five levels of ATC codes. A score, *TS*, is used to define the therapeutic similarity between two drugs:

where *n* ranges from 1 to 5. In this study, *n* = 3 is adopted considering that only a few drugs have the same ATC codes at the 5^{th} level.

### Drug combination prediction

We assume that two drugs are more likely to be combined if they share a large number of common drugs in the drug cocktail network. For example, if two drugs *d*_{
1
} and *d*_{2} with respective *n*_{1} and *n*_{2} partners have *m* in common in the drug cocktail network, there will be three groups in the neighborhood of the two drugs, i.e. (1) *m* drugs that are the neighbors of both drug *d*_{1} and *d*_{2}; (2) *n*_{1} - *m* partners that are the neighbors of drug *d*_{1} only; and (3) *n*_{2} - *m* partners are the neighbors of drug *d*_{2} only [45]. Suppose that there are totally *N* drugs in the drug combination network, then a *p*-value between *d*_{1} and *d*_{2} can be calculated using the following equation:

If two drugs share more common drugs compared with all of their neighbors, the *p*-value computed by equation (4) will be closer to 0, which means they are more likely to be combined. We use the equation (4) to compute the *p*-values for all possible combinations and then rank the values in ascending order. As drug pairs with lower *p*-values are more likely to be combined, the prediction of effective drug combinations can be made given a certain *p*-value threshold. We term this framework that explores the drug cocktail network and predicts possible drug combination as DCPred (Drug Combination Predictor) and assess its performance for inferring effective drug combinations based on the curated drug combinations dataset.

## References

Argiris A, Wang CX, Whalen SG, DiGiovanna MP: Synergistic interactions between tamoxifen and trastuzumab (Herceptin). Clinical Cancer Research. 2004, 10: 1409-1420. 10.1158/1078-0432.CCR-1060-02.

Osborne CK, Schiff R: Growth factor receptor cross-talk with estrogen receptor as a mechanism for tamoxifen resistance in breast cancer. Breast. 2003, 12: 362-367. 10.1016/S0960-9776(03)00137-1.

Marsh JC, Bertino JR, Katz KH, Davis CA, Durivage HJ, Rome LS, Richards F, Capizzi RL, Farber LR, Pasquale DN, et al: The influence of drug interval on the effect of methotrexate and fluorouracil in the treatment of advanced colorectal cancer. J Clin Oncol. 1991, 9: 371-380.

Wilson DR, Honrath U, Sonnenberg H: Interaction of amiloride and hydrochlorothiazide with atrial natriuretic factor in the medullary collecting duct. Can J Physiol Pharmacol. 1988, 66: 648-654. 10.1139/y88-101.

Frank J: Managing hypertension using combination therapy. American Family Physician. 2008, 77: 1279-1286.

Chan R, Park KC, Lee MH, Lee ES, Chang SE, Leow YH, Tay YK, Legarda-Montinola F, Tsai RY, Tsai TH, et al: A randomized controlled trial of the efficacy and safety of a fixed triple combination (fluocinolone acetonide 0.01%, hydroquinone 4%, tretinoin 0.05%) compared with hydroquinone 4% cream in Asian patients with moderate to severe melasma. Br J Dermatol. 2008, 159: 697-703.

Agrawal N, Pallos J, Slepko N, Apostol BL, Bodai L, Chang LW, Chiang AS, Thompson LM, Marsh JL: Identification of combinatorial drug regimens for treatment of Huntington's disease using Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 2005, 102: 3777-3781. 10.1073/pnas.0500055102.

Campostrini N, Marimpietri D, Totolo A, Mancone C, Fimia GM, Ponzoni M, Righetti PG: Proteomic analysis of anti-angiogenic effects by a combined treatment with vinblastine and rapamycin in an endothelial cell line. Proteomics. 2006, 6: 4420-4431. 10.1002/pmic.200600119.

Lehar J, Krueger AS, Avery W, Heilbut AM, Johansen LM, Price ER, Rickles RJ, Short GF, Staunton JE, Jin X, et al: Synergistic drug combinations tend to improve therapeutically relevant selectivity. Nature Biotechnology. 2009, 27: 659-666. 10.1038/nbt.1549.

Zimmermann GR, Lehar J, Keith CT: Multi-target therapeutics: when the whole is greater than the sum of the parts. Drug Discovery Today. 2007, 12: 34-42. 10.1016/j.drudis.2006.11.008.

Pennati M, Campbell AJ, Curto M, Binda M, Cheng YZ, Wang LZ, Curtin N, Golding BT, Griffin RJ, Hardcastle IR, et al: Potentiation of paclitaxel-induced apoptosis by the novel cyclin-dependent kinase inhibitor NU6140: a possible role for survivin down-regulation. Molecular Cancer Therapeutics. 2005, 4: 1328-1337. 10.1158/1535-7163.MCT-05-0022.

Lewis BR, Aoun SL, Bernstein GA, Crow SJ: Pharmacokinetic interactions between cyclosporine and bupropion or methylphenidate. Journal of Child and Adolescent Psychopharmacology. 2001, 11: 193-198. 10.1089/104454601750284117.

Tari L, Anwar S, Liang S, Cai J, Baral C: Discovering drug-drug interactions: a text-mining and reasoning approach based on properties of drug metabolism. Bioinformatics. 2010, 26: i547-553. 10.1093/bioinformatics/btq382.

Zhao XM, Wang RS, Chen L, Aihara K: Uncovering signal transduction networks from high-throughput data by integer linear programming. Nucleic Acids Res. 2008, 36: e48-10.1093/nar/gkn145.

Zhao XM, Wang RS, Chen L, Aihara K: Automatic modeling of signaling pathways by network flow model. J Bioinform Comput Biol. 2009, 7: 309-322. 10.1142/S0219720009004138.

Geva-Zatorsky N, Dekel E, Cohen AA, Danon T, Cohen L, Alon U: Protein Dynamics in Drug Combinations: a Linear Superposition of Individual-Drug Responses. Cell. 2010, 140: 643-651. 10.1016/j.cell.2010.02.011.

Calzolari D, Bruschi S, Coquin L, Schofield J, Feala JD, Reed JC, McCulloch AD, Paternostro G: Search Algorithms as a Framework for the Optimization of Drug Combinations. Plos Computational Biology. 2008, 4: e1000249-10.1371/journal.pcbi.1000249.

Jin G, Zhao H, Zhou X, Wong ST: An enhanced Petri-net model to predict synergistic effects of pairwise drug combinations from gene microarray data. Bioinformatics. 2011, 27: i310-i316. 10.1093/bioinformatics/btr202.

Wu Z, Zhao XM, Chen L: A systems biology approach to identify effective cocktail drugs. BMC Syst Biol. 2010, 4 (Suppl 2): S7-10.1186/1752-0509-4-S2-S7.

Zhao XM, Iskar M, Zeller G, Kuhn M, Noort V, Bork P: Prediction of drug combinations by integrating molecular and pharmacological data. Plos Computational Biology. 2011, 7: e1002323-10.1371/journal.pcbi.1002323.

Liu YB, Hu B, Fu CX, Chen X: DCDB: Drug combination database. Bioinformatics. 2010, 26: 587-588. 10.1093/bioinformatics/btp697.

Wishart DS, Knox C, Guo AC, Cheng D, Shrivastava S, Tzur D, Gautam B, Hassanali M: DrugBank: a knowledgebase for drugs, drug actions and drug targets. Nucleic Acids Research. 2008, 36: D901-D906.

Newman MEJ: The structure and function of complex networks. Siam Review. 2003, 45: 167-256. 10.1137/S003614450342480.

Maslov S, Sneppen K: Specificity and stability in topology of protein networks. Science. 2002, 296: 910-913. 10.1126/science.1065103.

Barabasi AL, Oltvai ZN: Network biology: understanding the cell's functional organization. Nature Reviews Genetics. 2004, 5: 101-113. 10.1038/nrg1272.

MacKay JH, Arcuri KE, Goldberg AI, Snapinn SM, Sweet CS: Losartan and low-dose hydrochlorothiazide in patients with essential hypertension - A double-blind, placebo-controlled trial of concomitant administration compared with individual components. Archives of Internal Medicine. 1996, 156: 278-285. 10.1001/archinte.1996.00440030072009.

Salmela PI, Juustila H, Kinnunen O, Koistinen P: Comparison of low doses of hydrochlorothiazide plus amiloride and hydrochlorothiazide alone in hypertension in elderly patients. Ann Clin Res. 1986, 18: 88-92.

Romond EH, Perez EA, Bryant J, Suman VJ, Geyer CE, Davidson NE, Tan-Chiu E, Martino S, Paik S, Kaufman PA, et al: Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer. New England Journal of Medicine. 2005, 353: 1673-1684. 10.1056/NEJMoa052122.

Piccart-Gebhart MJ, Procter M, Leyland-Jones B, Goldhirsch A, Untch M, Smith I, Gianni L, Baselga J, Bell R, Jackisch C, et al: Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer. New England Journal of Medicine. 2005, 353: 1659-1672. 10.1056/NEJMoa052306.

Jensen LJ, Kuhn M, Stark M, Chaffron S, Creevey C, Muller J, Doerks T, Julien P, Roth A, Simonovic M, et al: STRING 8-a global view on proteins and their functional interactions in 630 organisms. Nucleic Acids Research. 2009, 37: D412-D416. 10.1093/nar/gkn760.

Hand D: Measuring classifier performance: a coherent alternative to the area under the ROC curve. Machine Learning. 2009, 77: 103-123. 10.1007/s10994-009-5119-5.

Fawcett T: An introduction to ROC analysis. Pattern Recognition Letters. 2006, 27: 861-874. 10.1016/j.patrec.2005.10.010.

Delord JP, Pierga JY, Dieras V, Bertheault-Cvitkovic F, Turpin FL, Lokiec F, Lochon I, Chatelut E, Canal P, Guimbaud R, et al: A phase I clinical and pharmacokinetic study of capecitabine (Xeloda[reg]) and irinotecan combination therapy (XELIRI) in patients with metastatic gastrointestinal tumours. Br J Cancer. 2005, 92: 820-826. 10.1038/sj.bjc.6602354.

Garcia-Alfonso P, Munoz-Martin A, Mendez-Urena M, Quiben-Pereira R, Gonzalez-Flores E, Perez-Manga G: Capecitabine in combination with irinotecan (XELIRI), administered as a 2-weekly schedule, as first-line chemotherapy for patients with metastatic colorectal cancer: a phase II study of the Spanish GOTI group. Br J Cancer. 2009, 101: 1039-1043. 10.1038/sj.bjc.6605261.

Dent S, Messersmith H, Trudeau M: Gemcitabine in the management of metastatic breast cancer: a systematic review. Breast Cancer Research and Treatment. 2008, 108: 319-331. 10.1007/s10549-007-9610-z.

Chang J, Makris A, Gutierrez M, Hilsenbeck S, Hackett J, Jeong J, Liu M-L, Baker J, Clark-Langone K, Baehner F, et al: Gene expression patterns in formalin-fixed, paraffin-embedded core biopsies predict docetaxel chemosensitivity in breast cancer patients. Breast Cancer Research and Treatment. 2008, 108: 233-240. 10.1007/s10549-007-9590-z.

Levy C, Fumoleau P: Gemcitabine plus docetaxel: a new treatment option for anthracycline pretreated metastatic breast cancer patients?. Cancer Treatment Reviews. 2005, 31: S17-S22.

Wilhelm SM, Adnane L, Newell P, Villanueva A, Llovet JM, Lynch M: Preclinical overview of sorafenib, a multikinase inhibitor that targets both Raf and VEGF and PDGF receptor tyrosine kinase signaling. Molecular Cancer Therapeutics. 2008, 7: 3129-3140. 10.1158/1535-7163.MCT-08-0013.

Los M, Roodhart JML, Voest EE: Target practice: Lessons from phase III trials with bevacizumab and vatalanib in the treatment of advanced colorectal cancer. Oncologist. 2007, 12: 443-450. 10.1634/theoncologist.12-4-443.

Azad NS, Posadas EM, Kwitkowski VE, Steinberg SM, Jain L, Annunziata CM, Minasian L, Sarosy G, Kotz HL, Premkumar A, et al: Combination targeted therapy with sorafenib and bevacizumab results in enhanced toxicity and antitumor activity. Journal of Clinical Oncology. 2008, 26: 3709-3714. 10.1200/JCO.2007.10.8332.

Kumar S, Rajkumar SV: Thalidomide and lenalidomide in the treatment of multiple myeloma. European Journal of Cancer. 2006, 42: 1612-1622. 10.1016/j.ejca.2006.04.004.

Anderson KC: Lenalidomide and thalidomide: Mechanisms of action - Similarities and differences. Seminars in Hematology. 2005, 42: S3-S8.

Horrobin DF: A low toxicity maintenance regime, using eicosapentaenoic acid and readily available drugs, for mantle cell lymphoma and other malignancies with excess cyclin D1 levels. Medical Hypotheses. 2003, 60: 615-623. 10.1016/S0306-9877(03)00075-6.

Vallet S, Palumbo A, Raje N, Boccadoro M, Anderson KC: Thalidomide and lenalidomide: Mechanism-based potential drug combinations. Leuk Lymphoma. 2008, 49: 1238-1245. 10.1080/10428190802005191.

Samanta MP, Liang S: Predicting protein functions from redundancies in large-scale protein interaction networks. Proceedings of the National Academy of Sciences of the United States of America. 2003, 100: 12579-12583. 10.1073/pnas.2132527100.

## Acknowledgements

XMZ was partly supported by the Innovation Program of Shanghai Municipal Education Commission (10YZ01), Shanghai Rising-Star Program (10QA1402700), and National Natural Science Foundation of China (61103075, 91130032). JS was supported by the National Health and Medical Research Council of Australia (NHMRC) Peter Doherty Fellowship and the Hundred Talents Program of the Chinese Academy of Sciences (CAS). KJX was supported by the Innovation Program of Shanghai University (SHUCX112015).

This article has been published as part of *BMC Systems Biology* Volume 6 Supplement 1, 2012: Selected articles from The 5th IEEE International Conference on Systems Biology (ISB 2011). The full contents of the supplement are available online at http://www.biomedcentral.com/bmcsystbiol/supplements/6/S1.

## Author information

### Authors and Affiliations

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## Additional information

### Competing interests

The authors declare that they have no competing interests.

### Authors' contributions

KJX implemented the computational method, carried out data analysis, and drafted the manuscript under the direction of XMZ and JS. JS and XMZ guided and coordinated the project, and improved the presentation of the manuscript by copy-editing and fixing language issues. All authors read, revised and approved the final manuscript.

## Electronic supplementary material

### 12918_2012_874_MOESM5_ESM.doc

Additional file 5: Prediction performance of the DCPred1 model at varying thresholds, as measured by Sensitivity, Specificity and Accuracy. (DOC 30 KB)

### 12918_2012_874_MOESM6_ESM.doc

Additional file 6: Prediction performance of the DCPred2 model at varying thresholds, as measured by Sensitivity, Specificity and Accuracy. (DOC 30 KB)

### 12918_2012_874_MOESM7_ESM.doc

Additional file 7: Prediction performance of the DCPred3 model at varying thresholds, as measured by Sensitivity, Specificity and Accuracy. (DOC 30 KB)

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### Cite this article

Xu, KJ., Song, J. & Zhao, XM. The drug cocktail network.
*BMC Syst Biol* **6**
(Suppl 1), S5 (2012). https://doi.org/10.1186/1752-0509-6-S1-S5

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DOI: https://doi.org/10.1186/1752-0509-6-S1-S5