| Literature DB >> 29572227 |
Ping Zhu1,2, Yongzhang Liu3, Fenglin Zhang4, Xiufeng Bai1,2, Zilei Chen1,3, Fugen Shangguan1,3, Bo Zhang4, Lingyun Zhang1, Qianqian Chen2,4, Deyao Xie5, Linhua Lan3, Xiangdong Xue6, Xing-Jie Liang6, Bin Lu7, Taotao Wei8,4, Yan Qin9,2.
Abstract
Mitochondria regulate cellular bioenergetics and redox states and influence multiple signaling pathways required for tumorigenesis. In this study, we determined that the mitochondrial translation elongation factor 4 (EF4) is a critical component of tumor progression. EF4 was ubiquitous in human tissues with localization to the mitochondria (mtEF4) and performed quality control on respiratory chain biogenesis. Knockout of mtEF4 induced respiratory chain complex defects and apoptosis, while its overexpression stimulated cancer development. In multiple cancers, expression of mtEF4 was increased in patient tumor tissues. These findings reveal that mtEF4 expression may promote tumorigenesis via an imbalance in the regulation of mitochondrial activities and subsequent variation of cellular redox. Thus, dysregulated mitochondrial translation may play a vital role in the etiology and development of diverse human cancers.Significance: Dysregulated mitochondrial translation drives tumor development and progression. Cancer Res; 78(11); 2813-24. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 29572227 DOI: 10.1158/0008-5472.CAN-17-2059
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701