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PI3K activation is associated with intracellular sodium/iodide symporter protein expression in breast cancer

dc.contributor.authorKnostman, Katherin A. B.en_US
dc.contributor.authorMcCubrey, James A.en_US
dc.contributor.authorMorrison, Carl D.en_US
dc.contributor.authorZhang, Zhaoxiaen_US
dc.contributor.authorCapen, Charles C.en_US
dc.contributor.authorJhiang, Sissy M.en_US
dc.date.accessioned2011-04-15T15:19:23Zen_US
dc.date.accessioned2011-05-17T01:40:05Z
dc.date.available2011-04-15T15:19:23Zen_US
dc.date.available2011-05-17T01:40:05Z
dc.date.issued2007-07-25en_US
dc.description.abstractBackground: The sodium/iodide symporter (NIS) is a membrane glycoprotein mediating active iodide uptake in the thyroid gland and is the molecular basis for radioiodide imaging and therapeutic ablation of thyroid carcinomas. NIS is expressed in the lactating mammary gland and in many human breast tumors, raising interest in similar use for diagnosis and treatment. However, few human breast tumors have clinically evident iodide uptake ability. We previously identified PI3K signaling as important in NIS upregulation in transgenic mouse models of breast cancer, and the PI3K pathway is commonly activated in human breast cancer. Methods: NIS expression, subcellular localization, and function were analyzed in MCF-7 human breast cancer cells and MCF-7 cells stably or transiently expressing PI3K p110alpha subunit using Western blot of whole cell lysate, cell surface biotinylation Western blot and immunofluorescence, and radioiodide uptake assay, respectively. NIS localization was determined in a human breast cancer tissue microarray using immunohistochemical staining (IHC) and was correlated with preexisting pAkt IHC data. Statistical analysis consisted of Student's t-test (in vitro studies) or Fisher's Exact Test (in vivo correlational studies). Results: In this study, we demonstrate that PI3K activation in MCF-7 human mammary carcinoma cells leads to expression of underglycosylated NIS lacking cell surface trafficking necessary for iodide uptake ability. PI3K activation also appears to interfere with cell surface trafficking of exogenous NIS as well as all-trans retinoic acid-induced endogenous NIS. A correlation between NIS expression and upregulation of PI3K signaling was found in a human breast cancer tissue microarray. Conclusion: Thus, the PI3K pathway likely plays a major role in the discordance between NIS expression and iodide uptake in breast cancer patients. Further study is warranted to realize the application of NIS-mediated radioiodide ablation in breast cancer. Originally published BMC Cancer, Vol. 7, No. 137, July 2007en_US
dc.identifier.citationBMC Cancer; 7:137 p. 1-10en_US
dc.identifier.pmidPMC1963336en_US
dc.identifier.urihttp://hdl.handle.net/10342/3327en_US
dc.language.isoen_USen_US
dc.publisherEast Carolina Universityen_US
dc.relation.urihttp://www.biomedcentral.com/1471-2407/7/137en_US
dc.rightsAuthor notified of opt-out rights by Cammie Jennings prior to upload of this article.en_US
dc.subjectNISen_US
dc.subjectBreast--Canceren_US
dc.subjectPI3K signalingen_US
dc.titlePI3K activation is associated with intracellular sodium/iodide symporter protein expression in breast canceren_US
dc.typeArticleen_US

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