粒体自噬
帕金
MFN2型
品脱1
细胞生物学
赫拉
线粒体
癌细胞
程序性细胞死亡
MFN1型
自噬
细胞凋亡
细胞生长
溶酶体
夏普
化学
细胞
生物
线粒体融合
癌症
生物化学
半胱氨酸蛋白酶
医学
线粒体DNA
病理
酶
基因
遗传学
疾病
帕金森病
作者
Jiling Feng,Anahitasadat Mansouripour,Zhichao Xi,Li Zhang,Gang Xu,Hua Zhou,Hong‐Xi Xu
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-05-12
卷期号:26 (10): 2858-2858
被引量:13
标识
DOI:10.3390/molecules26102858
摘要
Nujiangexanthone A (NJXA), a bioactive component isolated from the leaves of Garcinia nujiangensis, has been reported to exhibit anti-inflammatory, antioxidant, and antitumor effects. Our previous work has shown that NJXA induced G0/1 arrest and apoptosis, thus suppressing cervical cancer cell growth. The present study provides new evidence that NJXA can induce cell death in HeLa cells by promoting mitophagy. We first identified that NJXA triggered GFP-LC3 and YFP-Parkin puncta accumulation, which are biomarkers of mitophagy. Moreover, NJXA degraded the mitochondrial membrane proteins Tom20 and Tim23 and mitochondrial fusion proteins MFN1 and MFN2, downregulated Parkin, and stabilized PINK1. Additionally, we revealed that NJXA induced lysosome degradation and colocalization of mitochondria and autophagosomes, which was attenuated by knocking down ATG7, the key regulator of mitophagy. Furthermore, since mitophagy is induced under starvation conditions, we detected the cytotoxic effect of NJXA in nutrient-deprived HeLa cells and observed better cytotoxicity. Taken together, our work contributes to the further clarification of the mechanism by which NJXA inhibits cervical cancer cell proliferation and provides evidence that NJXA has the potential to develop anticancer drugs.
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