He Dong-Xu, Xia Yu-Dong, Gu Xiao-Ting, Jin Jian, Ma Xin
National Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, Wuxi 214122, China.
E-GENE Technologies, Co., Ltd., Shenzhen 518083, China.
J Pharm Biomed Anal. 2015 Jan;102:500-8. doi: 10.1016/j.jpba.2014.10.018. Epub 2014 Oct 27.
Although chemotherapy is widely used to treat human cancers, most chemotherapeutic agents only benefit a small fraction of patients because of the heterogeneity of cancers. Therefore, identifying of the sensitivity of cancers toward various chemotherapies would be important for choosing of chemotherapeutic regime. In this study, a 23-gene chemoresistance signature was developed from chemoresistant breast cancers. Functions of the genes in the signature were related with transcription and translation. The signature was indicative of chemoresistance and associated with poor prognosis in multiple chemotherapeutic agents and cancer types. Furthermore, by applying computational approaches, we identified several compounds that might specifically affect the chemoresistant signature. Decitabine (DAC) was the compound most likely to target the signature. In vitro and clinical analysis confirmed effect of DAC toward both breast cancer cell lines and ovarian cancers respectively. In conclusion, our study identified a chemoresistant signature that is both predictive and prognostic, and the signature-related chemoresistance could be suppressed by DAC treatment.
尽管化疗被广泛用于治疗人类癌症,但由于癌症的异质性,大多数化疗药物仅使一小部分患者受益。因此,确定癌症对各种化疗的敏感性对于选择化疗方案至关重要。在本研究中,从化疗耐药的乳腺癌中开发了一种23基因的化疗耐药特征。该特征中的基因功能与转录和翻译有关。该特征表明化疗耐药,并与多种化疗药物和癌症类型的不良预后相关。此外,通过应用计算方法,我们鉴定了几种可能特异性影响化疗耐药特征的化合物。地西他滨(DAC)是最有可能靶向该特征的化合物。体外和临床分析分别证实了DAC对乳腺癌细胞系和卵巢癌的作用。总之,我们的研究鉴定了一种具有预测性和预后性的化疗耐药特征,并且DAC治疗可以抑制与该特征相关的化疗耐药。