粒体自噬
三阴性乳腺癌
癌症研究
癌变
线粒体
上睑下垂
自噬
化学
转移
细胞生物学
乳腺癌
生物
癌症
细胞凋亡
程序性细胞死亡
医学
内科学
生物化学
作者
Jing Xia,Changbin Chu,Wanqing Li,Hong Chen,Wenhua Xie,Rui Cheng,Kai Hu,Xi Li
摘要
Triple-negative breast cancer (TNBC) is a massive threat to women's health due to its high morbidity, malignancy, and the refractory, effective therapeutic option of TNBC is still deficient.The mitochondrial protein showed therapeutic potential on breast cancer, whereas the mechanism and downstream pathway of mitochondrial uncoupling protein 1 (UCP1) was not fully elucidated.We found that UCP1 was negatively regulated to the process of TNBC.Overexpressing UCP1 could inhibit the proliferation and metastasis of TNBC, meanwhile inducing the mitochondrial swelling and activation of mitophagy in vitro.Mitophagy activation was then assessed to elucidate whether it was downstream of UCP1 in TNBC metastasis.GSDME is the core of pyroptosis.We found that GSDME was activated in the TNBC cells when UCP1 levels were high.It regulates TNBC cell proliferation potential instead of the apoptosis process in vitro and in vivo.Our results suggested that UCP1 could inhibit the process of TNBC by activating mitophagy and pyroptosis.Impaired activation of mitophagy weakens the regulation effect of UCP1 on metastasis of TNBC, similar to the impairment of GSDME activation on the proliferation regulation of UCP1 on TNBC.UCP1 might be a novel therapeutic target of TNBC.
科研通智能强力驱动
Strongly Powered by AbleSci AI