Source:http://linkedlifedata.com/resource/pubmed/id/17885490
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-9-21
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pubmed:abstractText |
A 2-tier system that classifies ovarian serous carcinoma (OSC) as low grade or high grade is gaining acceptance. Women with low-grade OSC generally have higher 5-year survival rates than do women with high-grade OSC. We examined the expression of various markers to further understand the molecular differences between low-grade and high-grade OSCs: the potential therapeutic targets or prognostic markers Her-2/neu, estrogen receptor, and progesterone receptor (PR); the metastasis-associated markers cyclin D1 (BCL1), E-cadherin, matrix metalloproteinase (MMP) 2, and MMP-9; and the cell proliferation-associated markers BCL1, Ki-67 antigen (Ki-67), and p53. For this immunohistochemical analysis, we used paraffin-embedded specimens from 47 patients with advanced-stage low-grade OSC and from 49 patients with advanced-stage high-grade OSC. Our results showed that low-grade tumors expressed significantly higher levels of estrogen receptor, PR, and E-cadherin than did high-grade tumors, suggesting the involvement of gonadal steroid hormones, especially in the pathogenesis of low-grade OSC; the PR positivity was also observed in the stromal component of these low-grade tumors. On the other hand, high-grade tumors trended toward increased expression of MMP-9, BCL1, p53, and Ki-67, and robust MMP-9 positivity was observed in the stromal component of these high-grade tumors. These differences may lead to the development of different therapeutic strategies for women with either the low-grade or the high-grade form of OSC.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cadherins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Ki-67 Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 9,
http://linkedlifedata.com/resource/pubmed/chemical/PDRG1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Progesterone,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0277-1691
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pubmed:author |
pubmed-author:BodurkaDiane CDC,
pubmed-author:DeaversMichael TMT,
pubmed-author:GershensonDavid MDM,
pubmed-author:LuKaren HKH,
pubmed-author:MalpicaAnaisA,
pubmed-author:SchmandtRosemarie ERE,
pubmed-author:ShvartsmanHyun SHS,
pubmed-author:SilvaElvio GEG,
pubmed-author:ThorntonAngela DAD,
pubmed-author:WongKwong-KwokKK
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pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
404-9
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pubmed:dateRevised |
2007-12-3
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pubmed:meshHeading |
pubmed-meshheading:17885490-Cadherins,
pubmed-meshheading:17885490-Cystadenocarcinoma, Serous,
pubmed-meshheading:17885490-DNA-Binding Proteins,
pubmed-meshheading:17885490-Female,
pubmed-meshheading:17885490-Humans,
pubmed-meshheading:17885490-Immunohistochemistry,
pubmed-meshheading:17885490-Ki-67 Antigen,
pubmed-meshheading:17885490-Matrix Metalloproteinase 9,
pubmed-meshheading:17885490-Neoplasm Staging,
pubmed-meshheading:17885490-Ovarian Neoplasms,
pubmed-meshheading:17885490-Prognosis,
pubmed-meshheading:17885490-Receptors, Estrogen,
pubmed-meshheading:17885490-Receptors, Progesterone,
pubmed-meshheading:17885490-Tumor Markers, Biological
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pubmed:year |
2007
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pubmed:articleTitle |
Significantly greater expression of ER, PR, and ECAD in advanced-stage low-grade ovarian serous carcinoma as revealed by immunohistochemical analysis.
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pubmed:affiliation |
Department of Gynecologic Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA. kkwong@mdanderson.org
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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