ATG7 promotes the tumorigenesis of lung cancer but might be dispensable for prognosis predication: a clinicopathologic study

被引:17
作者
Sun, Shaoxing [1 ,2 ]
Wang, Zhihao [1 ,2 ]
Tang, Fang [1 ,2 ]
Hu, Pengchao [3 ]
Yang, Zetian [4 ]
Xue, Chao [4 ]
Gong, Jun [1 ,2 ]
Shi, Liu [1 ,2 ]
Xie, Conghua [1 ,2 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Radiat & Med Oncol, 169 Donghu Rd, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Zhongnan Hosp, Hubei Key Lab Tumor Biol Behav, Wuhan, Peoples R China
[3] Wuhan Univ, Sch Basic Med Sci, Dept Pathol & Pathophysiol, Wuhan, Peoples R China
[4] Wuhan Univ, Zhongnan Hosp, Dept Thorac & Cardiovasc Surg, Wuhan, Peoples R China
关键词
ATG7; autophagy; lung cancer; prognosis; clinicopathologic study; AUTOPHAGY MODULATION; CHLOROQUINE; TUMORS; CELLS; MACROAUTOPHAGY; HOMEOSTASIS; INHIBITOR; DISEASES; GROWTH; TARGET;
D O I
10.2147/OTT.S107876
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lung cancer is the most frequent cause of cancer-related death worldwide. Dysregulated autophagy is often observed in lung cancer. Autophagy-related 7 (ATG7) is an autophagy gene that is essential for the biogenesis of autophagosomes. Although ATG7-deficient mouse models have demonstrated that ATG7-dependent autophagy is required for lung cancer tumorigenesis, the relationship between ATG7 expression levels and human lung cancer is unclear. Here, we demonstrate that ATG7 was overexpressed in human lung cancer tissues compared with normal tissues. However, ATG7 expression was not associated with tumor differentiation, tumor size, or TNM stage. Moreover, the overexpression of ATG7 did not influence the overall survival of the lung cancer patients. Therefore, our results indicate that ATG7 might be dispensable for tumor growth and chemotherapy efficacy in human lung cancer.
引用
收藏
页码:4975 / 4981
页数:7
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