Cancer Research Meeting Calendar  Advances in Breast Cancer Research
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wang, L.
Right arrow Articles by Banerjee, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, L.
Right arrow Articles by Banerjee, S.
[Cancer Research 64, 7673-7677, November 1, 2004]
© 2004 American Association for Cancer Research


Advances in Brief

A Novel Nuclear Protein, MGC5306 Interacts with DNA Polymerase ß and Has a Potential Role in Cellular Phenotype

Liming Wang1, Nandan Bhattacharyya1, Diane M. Chelsea1, Pedro F. Escobar2 and Sipra Banerjee1,2

1 Department of Cancer Biology, Lerner Research Institute, Cleveland, Ohio; and 2 Department of Obstetrics and Gynecology, The Cleveland Clinic Foundation, Cleveland, Ohio

A novel protein MGC5306 has been identified in yeast–two-hybrid analysis by screening a HeLa cDNA library with a truncated DNA polymeraseß (polß{Delta}) as bait. The polß{Delta} is expressed in various types of cancers. Co-immunoprecipitation–Western blot analysis confirms not only its interaction with polß{Delta} but also with wild-type polß. Binding to polß indicates potential function of MGC5306 in repair pathway. Transfection of cells with MGC5306-GFP and Western blot analysis with anti-MGC5306 antibody reveal its nuclear localization. MGC5306 is expressed in human carcinomas and tumor cell lines but not in normal tissues, suggesting MGC5306 is most likely involved in carcinogenesis. An antigrowth activity and modulations of cell cycle events are identified in cells expressing siRNAMGC5306.




This article has been cited by other articles:


Home page
CarcinogenesisHome page
L. Wang, N. Bhattacharyya, T. Rabi, L. Wang, and S. Banerjee
Mammary carcinogenesis in transgenic mice expressing a dominant-negative mutant of DNA polymerase {beta} in their mammary glands
Carcinogenesis, June 1, 2007; 28(6): 1356 - 1363.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2004 by the American Association for Cancer Research.