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CDC45 promotes the stemness and metastasis in lung adenocarcinoma by affecting the cell cycle

细胞周期 癌症研究 基因敲除 生物 转移 肺癌 细胞生长 腺癌 癌症干细胞 癌症 肿瘤科 医学 细胞培养 遗传学
作者
Yafeng Liu,Tao Han,Zhijun Xu,Jing Wu,Jiawei Zhou,Jianqiang Guo,Rui Miao,Yingru Xing,Deyong Ge,Ying Bai,Hongyan Dong
出处
期刊:Journal of Translational Medicine [Springer Nature]
卷期号:22 (1)
标识
DOI:10.1186/s12967-024-05038-5
摘要

This study aimed to assess the functions of cell division cycle protein 45 (CDC45) in Non-small cell lung cancer (NSCLC) cancer and its effects on stemness and metastasis.Firstly, differentially expressed genes related to lung cancer metastasis and stemness were screened by differential analysis and lasso regression. Then, in vitro, experiments such as colony formation assay, scratch assay, and transwell assay were conducted to evaluate the impact of CDC45 knockdown on the proliferation and migration abilities of lung cancer cells. Western blotting was used to measure the expression levels of related proteins and investigate the regulation of CDC45 on the cell cycle. Finally, in vivo model with subcutaneous injection of lung cancer cells was performed to verify the effect of CDC45 on tumor growth.This study identified CDC45 as a key gene potentially influencing tumor stemness and lymph node metastasis. Knockdown of CDC45 not only suppressed the proliferation and migration abilities of lung cancer cells but also caused cell cycle arrest at the G2/M phase. Further analysis revealed a negative correlation between CDC45 and cell cycle-related proteins, stemness-related markers, and tumor mutations. Mouse experiments confirmed that CDC45 knockdown inhibited tumor growth.As a novel regulator of stemness, CDC45 plays a role in regulating lung cancer cell proliferation, migration, and cell cycle. Therefore, CDC45 may serve as a potential target for lung cancer treatment and provide a reference for further mechanistic research and therapeutic development.
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