基因沉默
细胞凋亡
细胞生物学
癌症研究
化学
生物
生物化学
基因
作者
Min Wu,Mengmeng Jin,Xiaohui Cao,Lei Zhao,Yonghuai Li
标识
DOI:10.2174/1568009623666230829143148
摘要
Finally, we concluded that the increased sensitivity to anlotinib in NSCLC/AR cells was achieved by knocking down TRIM29, besides, the positive effects of TRIM29 knockdown were attributed to the promotion of apoptosis via binding to RAD50 in NSCLC/AR cell nucleus. Therefore, TRIM29 might become a potential target for overcoming anlotinib resistance in NSCLC treatment.
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