Zhang Shirong, Wu Kan, Feng Jianguo, Wu Zhibing, Deng Qinghua, Guo Chao, Xia Bing, Zhang Jing, Huang Haixiu, Zhu Lucheng, Zhang Ke, Shen Binghui, Chen Xufeng, Ma Shenglin
Department of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, Hangzhou, China.
Department of Oncology, Affiliated Hangzhou First People's Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Oncotarget. 2016 Oct 18;7(42):68768-68780. doi: 10.18632/oncotarget.11967.
Metastasis is the reason for most cancer death, and a crucial primary step for cancer metastasis is invasion of the surrounding tissue, which may be initiated by some rare tumor cells that escape the heterogeneous primary tumor. In this study, we isolated invasive subpopulations of cancer cells from human non-small cell lung cancer (NSCLC) H460 and H1299 cell lines, and determined the gene expression profiles and the responses of these invasive cancer cells to treatments of ionizing radiation and chemotherapeutic agents. The subpopulation of highly invasive NSCLC cells showed epigenetic signatures of epithelial-mesenchymal transition, cancer cell stemness, increased DNA damage repair and cell survival signaling. We also investigated the epigenetic therapy potential of suberoylanilide hydroxamic acid (SAHA) on invasive cancer cells, and found that SAHA suppresses cancer cell invasiveness and sensitizes cancer cells to treatments of IR and chemotherapeutic agents. Our results provide guidelines for identification of metastatic predictors and for clinical management of NSCLC. This study also suggests a beneficial clinical potential of SAHA as a chemotherapeutic agent for NSCLC patients.
转移是大多数癌症死亡的原因,而癌症转移的一个关键起始步骤是侵袭周围组织,这可能由一些逃离异质性原发肿瘤的罕见肿瘤细胞引发。在本研究中,我们从人非小细胞肺癌(NSCLC)H460和H1299细胞系中分离出侵袭性癌细胞亚群,并确定了这些侵袭性癌细胞的基因表达谱以及它们对电离辐射和化疗药物治疗的反应。高侵袭性NSCLC细胞亚群表现出上皮-间质转化、癌细胞干性、DNA损伤修复增加和细胞存活信号的表观遗传特征。我们还研究了辛二酰苯胺异羟肟酸(SAHA)对侵袭性癌细胞的表观遗传治疗潜力,发现SAHA可抑制癌细胞侵袭,并使癌细胞对IR和化疗药物治疗敏感。我们的结果为NSCLC转移预测指标的鉴定和临床管理提供了指导。本研究还表明SAHA作为NSCLC患者化疗药物具有有益的临床潜力。