Stress granule: A promising target for cancer treatment

被引:72
作者
Gao, Xiaomeng [1 ]
Jiang, Li [1 ]
Gong, Yanling [1 ]
Chen, Xiaobing [1 ]
Ying, Meidan [1 ]
Zhu, Hong [1 ]
He, Qiaojun [1 ]
Yang, Bo [1 ]
Cao, Ji [1 ]
机构
[1] Zhejiang Univ, Zhejiang Prov Key Lab Anticanc Drug Res, Coll Pharmaceut Sci, Room 115, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSLATION INITIATION; MESSENGER-RNA; ENDORIBONUCLEASE G3BP; IN-VITRO; PROTEIN; PHOSPHORYLATION; INHIBITOR; UBIQUITIN; ACETYLATION; MECHANISMS;
D O I
10.1111/bph.14790
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Stress granules (SGs) are primarily composed of mRNAs that stall at translation initiation and usually appear in the cytoplasm under unusual physiological or pathological conditions such as hypoxia, oxidative stress, and viral infection. Recent studies have indicated that several components of SGs participate in tumourigenesis and cancer metastasis through tumour-associated signalling pathways as well as other mechanisms. Furthermore, some chemotherapy drugs have been reported to induce SGs. Thus, the roles of SGs in cancer treatment have attracted considerable interest. Importantly, disturbing the recruitment of SGs components or microtubule polymerization, as well as other strategies that can abolish SGs formation, is reported to inhibit tumour progression, suggesting that targeting SGs could be a promising strategy for cancer treatment. In this review, we summarize the relationship between SGs and cancer, as well as recent advances in targeting SGs, in the interest of providing new opportunities for cancer treatment.
引用
收藏
页码:4421 / 4433
页数:13
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