APOBEC3B, a molecular driver of mutagenesis in human cancers

Bibliographic Details
Title: APOBEC3B, a molecular driver of mutagenesis in human cancers
Authors: Jun Zou, Chen Wang, Xiangyi Ma, Edward Wang, Guang Peng
Source: Cell & Bioscience, Vol 7, Iss 1, Pp 1-7 (2017)
Publisher Information: BMC, 2017.
Publication Year: 2017
Collection: LCC:Biotechnology
LCC:Biology (General)
LCC:Biochemistry
Subject Terms: APOBEC, APOBEC3B, DNA editing, Mutagenesis, Human cancer, Biotechnology, TP248.13-248.65, Biology (General), QH301-705.5, Biochemistry, QD415-436
More Details: Abstract Human cancers results in large part from the accumulation of multiple mutations. The progression of premalignant cells is an evolutionary process in which mutations provide the fundamental driving force for genetic diversity. The increased mutation rate in premalignant cells allows selection for increased proliferation and survival and ultimately leads to invasion, metastasis, recurrence, and therapeutic resistance. Therefore, it is important to understand the molecular determinants of the mutational processes. Recent genome-wide sequencing data showed that apolipoprotein B mRNA editing catalytic polypeptide-like 3B (APOBEC3B) is a key molecular driver inducing mutations in multiple human cancers. APOBEC3B, a DNA cytosine deaminase, is overexpressed in a wide spectrum of human cancers. Its overexpression and aberrant activation lead to unexpected clusters of mutations in the majority of cancers. This phenomenon of clustered mutations, termed kataegis (from the Greek word for showers), forms unique mutation signatures. In this review, we will discuss the biological function of APOBEC3B, its tumorigenic role in promoting mutational processes in cancer development and the clinical potential to develop novel therapeutics by targeting APOBEC3B.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2045-3701
Relation: http://link.springer.com/article/10.1186/s13578-017-0156-4; https://doaj.org/toc/2045-3701
DOI: 10.1186/s13578-017-0156-4
Access URL: https://doaj.org/article/253c4c8d0f6b43869a75801fb7d1b0db
Accession Number: edsdoj.253c4c8d0f6b43869a75801fb7d1b0db
Database: Directory of Open Access Journals
More Details
ISSN:20453701
DOI:10.1186/s13578-017-0156-4
Published in:Cell & Bioscience
Language:English