Literature DB >> 22341651

The human gastric cancer-associated DNA polymerase β variant D160N is a mutator that induces cellular transformation.

Katherine A Donigan1, Suzanne E Hile, Kristin A Eckert, Joann B Sweasy.   

Abstract

Approximately 30% of human tumors sequenced to date harbor mutations in the POLB gene that are not present in matched normal tissue. Many mutations give rise to enzymes that contain non-synonymous single amino acid substitutions, several of which have been found to have aberrant activity or fidelity and transform cells when expressed. The DNA Polymerase β (Pol β) variant Asp160Asn (D160N) was first identified in a gastric tumor. Expression of D160N in cells induces cellular transformation as measured by hyperproliferation, focus formation, anchorage-independent growth and invasion. Here, we show that D160N is an active mutator polymerase that induces complex mutations. Our data support the interpretation that complex mutagenesis is the underlying mechanism of the observed cellular phenotypes, all of which are linked to tumorigenesis or tumor progression.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22341651      PMCID: PMC3624760          DOI: 10.1016/j.dnarep.2012.01.004

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  34 in total

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3.  Functional mutation of DNA polymerase beta found in human gastric cancer--inability of the base excision repair in vitro.

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5.  What is a microsatellite: a computational and experimental definition based upon repeat mutational behavior at A/T and GT/AC repeats.

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6.  AP endonuclease-independent DNA base excision repair in human cells.

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  17 in total

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Review 2.  Base excision repair: a critical player in many games.

Authors:  Susan S Wallace
Journal:  DNA Repair (Amst)       Date:  2014-04-26

3.  Single molecule glycosylase studies with engineered 8-oxoguanine DNA damage sites show functional defects of a MUTYH polyposis variant.

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5.  The E288K colon tumor variant of DNA polymerase β is a sequence specific mutator.

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6.  Base Excision Repair Variants in Cancer.

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7.  DNA Polymerase β Cancer-Associated Variant I260M Exhibits Nonspecific Selectivity toward the β-γ Bridging Group of the Incoming dNTP.

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8.  Transcriptional profiling reveals elevated Sox2 in DNA polymerase ß null mouse embryonic fibroblasts.

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9.  Irreversible inhibition of DNA polymerase β by small-molecule mimics of a DNA lesion.

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