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Accession Number:
ADA436875
Title:
Exploring a Link Between NF-KB and G2/M Cell Cycle Arrest in Breast Cancer Cells
Descriptive Note:
Annual summary rept. 1 Apr 2004-31 Mar 2005
Corporate Author:
WISCONSIN UNIV-MADISON
Report Date:
2005-04-01
Pagination or Media Count:
28.0
Abstract:
The purpose of this grant is to understand how activation of the NF-kBRel family of transcription factors leads to breast cancer cell survival following treatment with radiation. The NF-kBRel family of transcription factors are known to greatly affect survival of various cancer cell types, including breast cancer cells. Our hypothesis is that activation of NF-kB in breast cancer cells contributes to a G2M cell cycle arrest, affording these cells extra opportunity to repair damaged DNA and thus allowing them to evade death inducing effects of radiation. Cell cycle analysis and levels of apoptosis were determined following exposure to ionizing irradiation. Cells capable of NF-kB activation efficiently arrested in G2M cell cycle phase while those that are not capable of activating NF-kB, do not efficiently arrest. Using RPA analysis we identified a gene, p2lwat1cip1, and have now shown that it is involved in maintaining the G2M phase cell cycle arrest following IR. Through the use of stable RNAi interference, we found that the G2M arrest is partially dependent on p2lWatlCipl. Understanding how NF-kB is activated and how NF-KB provides protection from cell death will be important for designing strategies to circumvent this resistance mechanism to improve efficacy of radiation therapy.
Distribution Statement:
APPROVED FOR PUBLIC RELEASE
