Radiotherapy diagnostic biomarkers in radioresistant human H460 lung cancer stem-like cells

被引:35
作者
Yun, Hong Shik [1 ,2 ]
Baek, Jeong-Hwa [1 ,3 ]
Yim, Ji-Hye [1 ]
Um, Hong-Duck [1 ]
Park, Jong Kuk [1 ]
Song, Jie-Young [1 ]
Park, In-Chul [1 ]
Kim, Jae-Sung [1 ]
Lee, Su-Jae [1 ]
Lee, Chang-Woo [3 ]
Hwang, Sang-Gu [1 ]
机构
[1] Korea Inst Radiol & Med Sci, Div Radiat Canc Biol, Seoul, South Korea
[2] Hanyang Univ, Coll Nat Sci, Dept Life Sci, Seoul 133791, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Dept Mol & Cell Biol, Suwon, South Korea
基金
新加坡国家研究基金会;
关键词
Biomarker; cancer stem-like cells; diagnose; H460 lung cancer cells; proteomics; radioresistance; radiotherapy; RADIATION; RADIOSENSITIVITY; EXPRESSION; APOPTOSIS; PROTEINS; IDENTIFICATION; INHIBITION; RESISTANCE; DEPLETION; CONFERS;
D O I
10.1080/15384047.2016.1139232
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor cell radioresistance is a major contributor to radiotherapy failure, highlighting the importance of identifying predictive biomarkers for radioresistance. In this work, we established a radioresistant H460 (RR-H460) cell line from parental radiosensitive H460 lung cancer cells by exposure to fractionated radiation. The radiation-resistant, anti-apoptotic phenotype of RR-H460 cell lines was confirmed by their enhanced clonogenic survival and increased expression of the radioresistance genes Hsp90 and Her-3. RR-H460 cells displayed characteristics of cancer stem-like cells (CSCs), including induction of the surface marker CD44 and stem cell markers Nanog, Oct4, and Sox2. RR-H460 cells also exhibited sphere formation and malignant behavior, further supporting a CSC phenotype. Using proteomic analyses, we identified 8 proteins that were up-regulated in RR-H460 CSC lines and therefore potentially involved in radioresistance and CSC-related biological processes. Notably, 4 of thesePAI-2, NOMO2, KLC4, and PLOD3have not been previously linked to radioresistance. Depletion of these individual genes sensitized RR-H460 cells to radiotoxicity and additively enhancing radiation-induced apoptosis. Our findings suggest the possibility of integrating molecular targeted therapy with radiotherapy as a strategy for resolving the radioresistance of lung tumors.
引用
收藏
页码:208 / 218
页数:11
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