内斯汀
生物
基因敲除
线粒体
细胞生物学
癌症研究
间质细胞
细胞凋亡
干细胞
神经干细胞
生物化学
作者
Jing Wang,Jianye Cai,Yinong Huang,Qiong Ke,Bingyuan Wu,S Wang,Xiao‐Jian Han,T Wang,Y Wang,W Li,Chunyan Lao,Song Wu,Andy Peng Xiang
出处
期刊:Oncogene
[Springer Nature]
日期:2015-10-05
卷期号:35 (24): 3139-3150
被引量:23
摘要
Nestin is widely expressed in numerous tumors and has become a diagnostic and prognostic indicator. However, the exact mechanism by which nestin contributes to tumor malignancy remains poorly understood. Here, we found marked upregulation of nestin expression in highly proliferative and invasive gastrointestinal stromal tumor (GIST) specimens. Nestin knockdown in GIST cells reduced the proliferative and invasive activity owing to a decrease of mitochondrial intracellular reactive oxygen species (ROS) generation. Furthermore, nestin was co-localized with mitochondria, and knockdown of nestin increased mitochondrial elongation and influenced the mitochondrial function, including oxygen consumption rates, ATP generation and mitochondrial membrane potential and so on. In exploring the underlying mechanism, we demonstrated nestin knockdown inhibited the mitochondrial recruitment of Dynamin-related protein1 and induced the change of mitochondrial dynamics. Thus, nestin may have an important role in GIST malignancy by regulating mitochondrial dynamics and altering intracellular ROS levels. The findings provide new clues to reveal mechanisms by which nestin mediates the proliferation and invasion of GISTs.
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