<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-24T17:51:25Z</responseDate><request verb="GetRecord" identifier="oai:ruor.uottawa.ca:10393/6361" metadataPrefix="oai_dc">https://ruor.uottawa.ca/server/oai/request</request><GetRecord><record><header><identifier>oai:ruor.uottawa.ca:10393/6361</identifier><datestamp>2024-02-23T08:57:01Z</datestamp><setSpec>com_10393_242</setSpec><setSpec>col_10393_244</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Mechanisms of 17-beta-estradiol regulation of the proto-oncogene  Bcl-2 in MCF-7 human breast cancer cells.</dc:title>
   <dc:creator>Kushwaha, Neena.</dc:creator>
   <dc:contributor>Pratt, Christine,</dc:contributor>
   <dc:subject>Biology, Molecular.</dc:subject>
   <dc:description>In the present studies, the mechanisms of estrogen regulation of Bcl-2 were investigated by analyzing the expression of different Bcl-2 promoter-driven constructs stably transfected into MCF-7 cells. An approximately 1.7 kilobase (kb) sequence which directed estrogen-dependent regulation of  Bcl-2 expression in these stable MCF-7 clones was identified. Another agent which may play a role in the regulation of Bcl-2 expression is the tumour suppressor gene, p53. We investigated the effects of various mutant p53 proteins and low levels of p53 on Bcl-2 expression in MCF-7 cells. Neither MCF-7/E6 cells expressing virtually undetectable levels of p53 nor MCF-7/173L cells expressing a DNA binding domain mutant p53, showed altered E2-mediated induction of Bcl-2 mRNA or protein levels. However, MCF-7 cells expressing a truncated mutant p53 protein (Delta291) resulted in a dramatic decrease in Bcl-2 protein levels, but not mRNA levels, upon E2 treatment. These results suggest that a p53 protein lacking a carboxy-terminus may cooperate with E2 post-transcriptionally to negatively regulate Bcl-2 levels in MCF-7 human breast cancer cells. (Abstract shortened by UMI.)</dc:description>
   <dc:date>2009-03-23T13:06:53Z</dc:date>
   <dc:date>2009-03-23T13:06:53Z</dc:date>
   <dc:date>2002</dc:date>
   <dc:date>2002</dc:date>
   <dc:type>Thesis</dc:type>
   <dc:identifier>Source: Masters Abstracts International, Volume: 40-05, page: 1198.</dc:identifier>
   <dc:identifier>9780612660663</dc:identifier>
   <dc:identifier>http://hdl.handle.net/10393/6361</dc:identifier>
   <dc:identifier>http://dx.doi.org/10.20381/ruor-11230</dc:identifier>
   <dc:format>99 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>University of Ottawa (Canada)</dc:publisher>
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