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dc.contributor.authorTaniguchi, Cullen M.
dc.contributor.authorWinnay, Jonathon
dc.contributor.authorKondo, Tatsuya
dc.contributor.authorBronson, Roderick T.
dc.contributor.authorGuimaraes, Alexander R.
dc.contributor.authorAleman, Jose O.
dc.contributor.authorLuo, Ji
dc.contributor.authorStephanopoulos, Gregory
dc.contributor.authorWeissleder, Ralph
dc.contributor.authorCantley, Lewis C.
dc.contributor.authorKahn, C. Ronald
dc.date.accessioned2013-06-20T19:34:24Z
dc.date.available2013-06-20T19:34:24Z
dc.date.issued2010-06
dc.date.submitted2010-04
dc.identifier.issn0008-5472
dc.identifier.issn1538-7445
dc.identifier.urihttp://hdl.handle.net/1721.1/79358
dc.description.abstractPhosphoinositide 3-kinase (PI3K) plays a critical role in tumorigenesis, and the PI3K p85 regulatory subunit exerts both positive and negative effects on signaling. Expression of Pik3r1, the gene encoding p85, is decreased in human prostate, lung, ovarian, bladder, and liver cancers, consistent with the possibility that p85 has tumor suppressor properties. We tested this hypothesis by studying mice with a liver-specific deletion of the Pik3r1 gene. These mice exhibited enhanced insulin and growth factor signaling and progressive changes in hepatic pathology, leading to the development of aggressive hepatocellular carcinomas with pulmonary metastases. Liver tumors that arose exhibited markedly elevated levels of phosphatidylinositol (3,4,5)-trisphosphate, along with Akt activation and decreased PTEN expression, at both the mRNA and protein levels. Together, these results substantiate the concept that the p85 subunit of PI3K has a tumor-suppressive role in the liver and possibly other tissues. Cancer Res; 70(13); 5305–15.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant DK33201)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant DK55545)en_US
dc.description.sponsorshipJoslin Diabetes Center (Joslin Diabetes and Endocrinology Research Center grant DK34834)en_US
dc.description.sponsorshipJoslin Diabetes Center (Joslin Diabetes and Endocrinology Research Center grant GM41890)en_US
dc.description.sponsorshipJoslin Diabetes Center (Joslin Diabetes and Endocrinology Research Center grant CA089021)en_US
dc.description.sponsorshipSouthern Association for Institutional Research (grant 2U24CA092782-07)en_US
dc.description.sponsorshipAmerican Diabetes Association (Medical Scholars Award)en_US
dc.description.sponsorshipHarvard Medical School (Medical Scientist Training Program Scholarship)en_US
dc.language.isoen_US
dc.publisherAmerican Association for Cancer Researchen_US
dc.relation.isversionofhttp://dx.doi.org/10.1158/0008-5472.CAN-09-3399en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleThe Phosphoinositide 3-Kinase Regulatory Subunit p85  Can Exert Tumor Suppressor Properties through Negative Regulation of Growth Factor Signalingen_US
dc.typeArticleen_US
dc.identifier.citationTaniguchi, C. M., J. Winnay, T. Kondo, R. T. Bronson, A. R. Guimaraes, J. O. Aleman, J. Luo, et al. The Phosphoinositide 3-Kinase Regulatory Subunit p85  Can Exert Tumor Suppressor Properties Through Negative Regulation of Growth Factor Signaling. Cancer Research 70, no. 13 (June 30, 2010): 5305-5315.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorStephanopoulos, Gregoryen_US
dc.contributor.mitauthorAleman, Jose O.en_US
dc.relation.journalCancer Researchen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsTaniguchi, C. M.; Winnay, J.; Kondo, T.; Bronson, R. T.; Guimaraes, A. R.; Aleman, J. O.; Luo, J.; Stephanopoulos, G.; Weissleder, R.; Cantley, L. C.; Kahn, C. R.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-6909-4568
dspace.mitauthor.errortrue
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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