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. 2022 Aug 25;13:949314. doi: 10.3389/fgene.2022.949314

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Copyright © 2022 Cai, Ji, Wu, Chen, Zheng, Chen, Zhang, Xie, Huang, Chen, Lin, Lin, Chen and Li.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Comparison of potential therapeutic drug susceptibility among the three different subgroups as assessed by IC50. (A) AZD.2281. (B) AZD6244. (C) BMS.754807. (D) Bosutinib. (E) Bryostatin.1. (F) CCT007093. (G) CGP.60474. (H) CI.1040. (I) Etoposide. (J) GDC.0449. (K) Gefitinib. (L) Gemcitabine. (M) GSK269962A. (N) GW.441756. (O) JNK.9L. (P) KIN001.135. (Q) LFM.A13. (R) Pyrimethamine. (S) Roscovitine. (T) Temsirolimus. Top 20 significantly associations were displayed, as determined by the p-value. IC50, the half-maximal inhibitory concentration.