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Feedback regulation of telomerase reverse transcriptase: new insight into the evolving field of telomerase in cancer.

Feedback regulation of telomerase reverse transcriptase: new insight into the evolving field of telomerase in cancer.

Authors :
Wu, Xiao-qin
Huang, Cheng
He, Xu
Tian, Yuan-yao
Zhou, De-xi
He, Yong
Liu, Xin-hua
Li, Jun
Source :
Cellular Signalling. Dec2013, Vol. 25 Issue 12, p2462-2468. 7p.
Publication Year :
2013

Abstract

Abstract: Telomerase reverse transcriptase (TERT) is the catalytic component of telomerase, especially the rate-limiting determinant of telomerase activity. So far, TERT has been reported to be over-expressed in more than 90% of cancers, thereby playing a critical role in sustained proliferation and survival potentials of various cancer cells. Over the past decade, a comprehensive network of transcription factors has been shown to be involved in the regulation of TERT. Furthermore, accumulating evidence has suggested that TERT could modulate the expression of numerous genes involved in diverse group of cellular processes, including cell cycle regulation and cellular signaling. Therefore, it indicates that TERT is both an effector and a regulator in carcinoma. However, the mechanisms of the interaction between TERT and its target genes are still not fully understood. Thus, it is necessary to consolidate and summarize recent developments of the cross-talk between TERT and related genes in cancer cells or other cells with cancer cell characteristics, and elucidate these relevant mechanisms. In this review, we focus on various signaling pathways and genes that participate in the feedback regulation of TERT and the underlying feedback loop mechanism of TERT, further providing new insights into non-telomeric functions of telomerase and potentially to be used as a novel therapeutic target for cancer. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
08986568
Volume :
25
Issue :
12
Database :
Academic Search Index
Journal :
Cellular Signalling
Publication Type :
Academic Journal
Accession number :
91267348
Full Text :
https://doi.org/10.1016/j.cellsig.2013.08.009