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dc.identifier.urihttp://hdl.handle.net/11401/76900
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeThesis
dcterms.abstractBreast cancer is the most common cancer in women and metastasis is the primary cause for mortality. Matrix metalloproteinases (MMPs) play important roles in cancer cell migration and invasion. Tumor suppressor gene TP53 is the most frequently mutated gene in cancer, and p53 mutation occurs in invasive breast cancer with higher frequency than in non-invasive breast cancer. However, the nature of relationship between p53 and MMPs remains inconclusive. Here we show that wild type p53 could repress transcriptional activity of MMP-9 and MMP-14, while the DNA-contact mutant p53 R280K could upregulate the transcription of MMP-9 and MMP-14. This regulation might be Sp1-dependent as there is a p53/Sp1 overlapping binding site on the promoters of MMP-9 and MMP-14. Although additional study is needed to further confirm this mechanism, our finding would provide a potential target for anti-metastatic therapy.
dcterms.available2017-09-20T16:51:24Z
dcterms.contributorCao, Jianen_US
dcterms.contributorMao, Cungui.en_US
dcterms.creatorXue, Yingjiao
dcterms.dateAccepted2017-09-20T16:51:24Z
dcterms.dateSubmitted2017-09-20T16:51:24Z
dcterms.descriptionDepartment of Biochemistry and Cell Biologyen_US
dcterms.extent29 pg.en_US
dcterms.formatApplication/PDFen_US
dcterms.formatMonograph
dcterms.identifierhttp://hdl.handle.net/11401/76900
dcterms.issued2016-12-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:51:24Z (GMT). No. of bitstreams: 1 Xue_grad.sunysb_0771M_13101.pdf: 1229735 bytes, checksum: d646fa0a1db0fd27ec1ac47defcf44b9 (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectMolecular biology
dcterms.titleTranscriptional Regulation of MMP-9 and MMP-14 by p53 and its Mutant R280K
dcterms.typeThesis


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