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Decreased galectin-3 expression in prostate cancer

dc.contributor.authorPacis, Ronald A.en_US
dc.contributor.authorPilat, Mary Josephine P.en_US
dc.contributor.authorPienta, Kenneth J.en_US
dc.contributor.authorWojno, Kirk J.en_US
dc.contributor.authorRaz, Avrahamen_US
dc.contributor.authorHogan, Victoren_US
dc.contributor.authorCooper, Carlton R.en_US
dc.date.accessioned2006-04-19T13:48:51Z
dc.date.available2006-04-19T13:48:51Z
dc.date.issued2000-07-01en_US
dc.identifier.citationPacis, Ronald A.; Pilat, Mary Josephine; Pienta, Kenneth J.; Wojno, Kirk; Raz, Avraham; Hogan, Victor; Cooper, Carlton R. (2000)."Decreased galectin-3 expression in prostate cancer." The Prostate 44(2): 118-123. <http://hdl.handle.net/2027.42/34754>en_US
dc.identifier.issn0270-4137en_US
dc.identifier.issn1097-0045en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34754
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10881021&dopt=citationen_US
dc.description.abstractBACKGROUND Galectin-3 is a carbohydrate-binding protein whose level of expression has been shown to be correlated with metastatic potential in a number of different tumor types. The purpose of this investigation was to examine galectin-3 expression in several tumorigenic and nontumorigenic prostate cell lines and prostate tissue samples. METHODS The expression of galectin-3 in cell lines and tissue samples was evaluated by tissue immunohistochemistry and Western blot analysis. RESULTS Human cell lines PC-3M, PC-3, DU-145, PrEC-1, and MCF10A demonstrated the presence of galectin-3. Galectin-3 was not detected in TSU-pr1 and LNCaP by Western blot analysis. We furthered our studies by examining a series of human prostate tissue samples for expression of galectin-3. Overall, approximately 60–70% of the normal tissue examined demonstrated heterogenous expression of galectin-3. In stage II tumors, however, there was a dramatic decrease in galectin-3 expression in both PIN and tumor sections, with only 10.5% (2/19) of these samples expressing this protein. Stage III tumors also demonstrated a decreased expression of galectin-3, although this downregulation was not as dramatic, with 35% of PIN samples and 52% of tumor tissue expressing galectin-3 ( P < 0.01). CONCLUSIONS These data demonstrate that galectin-3 is downregulated in prostate cancer. The altered downregulation pattern of galectin-3 observed between tumor stages suggests different roles for galectin-3 in the progression of prostate cancer. Prostate 44:118–123, 2000. © 2000 Wiley-Liss, Inc.en_US
dc.format.extent1605678 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleDecreased galectin-3 expression in prostate canceren_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Internal Medicine, St. John's Hospital, Detroit, Michiganen_US
dc.contributor.affiliationumUniversity of Michigan Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Internal Medicine, St. John's Hospital, Detroit, Michiganen_US
dc.contributor.affiliationumUniversity of Michigan Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Internal Medicine, St. John's Hospital, Detroit, Michigan ; Section of Urology, Department of Surgery, St. John's Hospital, Detroit, Michigan ; Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan Comprehensive Cancer Center, 1500 East Medical Center Drive-7308 CCGC, Ann Arbor, MI 48109-0946en_US
dc.contributor.affiliationumUniversity of Michigan Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Internal Medicine, St. John's Hospital, Detroit, Michigan ; Department of Pathology, St. John's Hospital, Detroit, Michiganen_US
dc.contributor.affiliationumUniversity of Michigan Comprehensive Cancer Center, Division of Hematology/Oncology, Department of Internal Medicine, St. John's Hospital, Detroit, Michiganen_US
dc.contributor.affiliationotherKarmanos Cancer Institute and Wayne State University, Detroit, Michiganen_US
dc.contributor.affiliationotherKarmanos Cancer Institute and Wayne State University, Detroit, Michiganen_US
dc.identifier.pmid10881021en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34754/1/4_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1097-0045(20000701)44:2<118::AID-PROS4>3.0.CO;2-Uen_US
dc.identifier.sourceThe Prostateen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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