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Article: Proteomic analysis of a preneoplastic phenotype in ovarian surface epithelial cells derived from prophylactic oophorectomies
Title | Proteomic analysis of a preneoplastic phenotype in ovarian surface epithelial cells derived from prophylactic oophorectomies |
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Authors | |
Keywords | BRCA1 Hereditary Ovarian cancers Ovarian surface epithelium |
Issue Date | 2005 |
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygyno |
Citation | Gynecologic Oncology, 2005, v. 98 n. 1, p. 68-76 How to Cite? |
Abstract | Objective. To study the pattern of protein expression associated with a predisposition to develop ovarian cancer. Methods. Prophylactic oophorectomy is used to prevent ovarian carcinoma in high-risk populations who have a strong family history of breast/ovarian cancer. In ovarian specimens of these women, the ovarian surface epithelium (OSE), which is tissue of origin of epithelial ovarian cancer, often shows altered morphology, growth patterns and differentiation features that are believed to be preneoplastic. This study has used a proteomic approach, based on two-dimensional gel electrophoresis and mass spectrometry, to compare the protein profiles of OSE from women with a history of familial ovarian cancer (FH-OSE), i.e., at least two first-degree relatives with such cancer and/or testing positive for BRCA1 mutations, to those without such history (NFH-OSE). Results. Of >1500 protein spots, there were 8 proteins whose levels were significantly altered in FH-OSE. Three were known ovarian tumor associated proteins, others were novel changes. A number of the alterations seen were accompanied with protein modifications and have not been previously reported. There was a predominance of sequences related to the stress response pathway. Differential expression of selected genes was confirmed by Western blotting and real-time reverse transcription polymerase chain reaction. Conclusions. Our findings define the OSE phenotype of women at a high risk of developing ovarian cancer. Protein alterations seen in these tissues may represent an early, irreversible, non-mutational step in ovarian epithelial neoplastic progression and may be potential early and sensitive markers for the evaluation of cancer risk. © 2005 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/48511 |
ISSN | 2023 Impact Factor: 4.5 2023 SCImago Journal Rankings: 1.627 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | He, QY | en_HK |
dc.contributor.author | Zhou, Y | en_HK |
dc.contributor.author | Wong, E | en_HK |
dc.contributor.author | Ehlen, TG | en_HK |
dc.contributor.author | Auersperg, N | en_HK |
dc.contributor.author | Chiu, JF | en_HK |
dc.contributor.author | Wong, AST | en_HK |
dc.date.accessioned | 2008-05-22T04:15:52Z | - |
dc.date.available | 2008-05-22T04:15:52Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Gynecologic Oncology, 2005, v. 98 n. 1, p. 68-76 | en_HK |
dc.identifier.issn | 0090-8258 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/48511 | - |
dc.description.abstract | Objective. To study the pattern of protein expression associated with a predisposition to develop ovarian cancer. Methods. Prophylactic oophorectomy is used to prevent ovarian carcinoma in high-risk populations who have a strong family history of breast/ovarian cancer. In ovarian specimens of these women, the ovarian surface epithelium (OSE), which is tissue of origin of epithelial ovarian cancer, often shows altered morphology, growth patterns and differentiation features that are believed to be preneoplastic. This study has used a proteomic approach, based on two-dimensional gel electrophoresis and mass spectrometry, to compare the protein profiles of OSE from women with a history of familial ovarian cancer (FH-OSE), i.e., at least two first-degree relatives with such cancer and/or testing positive for BRCA1 mutations, to those without such history (NFH-OSE). Results. Of >1500 protein spots, there were 8 proteins whose levels were significantly altered in FH-OSE. Three were known ovarian tumor associated proteins, others were novel changes. A number of the alterations seen were accompanied with protein modifications and have not been previously reported. There was a predominance of sequences related to the stress response pathway. Differential expression of selected genes was confirmed by Western blotting and real-time reverse transcription polymerase chain reaction. Conclusions. Our findings define the OSE phenotype of women at a high risk of developing ovarian cancer. Protein alterations seen in these tissues may represent an early, irreversible, non-mutational step in ovarian epithelial neoplastic progression and may be potential early and sensitive markers for the evaluation of cancer risk. © 2005 Elsevier Inc. All rights reserved. | en_HK |
dc.format.extent | 70427 bytes | - |
dc.format.extent | 254114 bytes | - |
dc.format.mimetype | application/pdf | - |
dc.format.mimetype | application/pdf | - |
dc.language | eng | en_HK |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygyno | en_HK |
dc.relation.ispartof | Gynecologic Oncology | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | BRCA1 | en_HK |
dc.subject | Hereditary | en_HK |
dc.subject | Ovarian cancers | en_HK |
dc.subject | Ovarian surface epithelium | en_HK |
dc.title | Proteomic analysis of a preneoplastic phenotype in ovarian surface epithelial cells derived from prophylactic oophorectomies | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0090-8258&volume=98&spage=68&epage=76&date=2005&atitle=Proteomic+analysis+of+a+preneoplastic+phenotype+in+ovarian+surface+epithelial+cells+derived+from+prophylactic+oophorectomies | en_HK |
dc.identifier.email | Wong, AST: awong1@hkucc.hku.hk | en_HK |
dc.identifier.authority | Wong, AST=rp00805 | en_HK |
dc.description.nature | postprint | en_HK |
dc.identifier.doi | 10.1016/j.ygyno.2005.04.002 | en_HK |
dc.identifier.pmid | 15913737 | - |
dc.identifier.scopus | eid_2-s2.0-20444502473 | en_HK |
dc.identifier.hkuros | 101945 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-20444502473&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 98 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 68 | en_HK |
dc.identifier.epage | 76 | en_HK |
dc.identifier.isi | WOS:000230284200012 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | He, QY=34770287900 | en_HK |
dc.identifier.scopusauthorid | Zhou, Y=7405366890 | en_HK |
dc.identifier.scopusauthorid | Wong, E=23101622300 | en_HK |
dc.identifier.scopusauthorid | Ehlen, TG=6603203782 | en_HK |
dc.identifier.scopusauthorid | Auersperg, N=7006582556 | en_HK |
dc.identifier.scopusauthorid | Chiu, JF=7201501692 | en_HK |
dc.identifier.scopusauthorid | Wong, AST=23987963300 | en_HK |
dc.identifier.issnl | 0090-8258 | - |