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Differential expression patterns of a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) -1, -4, -5, and -14 in human placenta and gestational trophoblastic diseases.
DC Field | Value | Language |
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dc.contributor.author | Lee, SY | - |
dc.contributor.author | Lee, HS | - |
dc.contributor.author | Gil, M | - |
dc.contributor.author | Kim, CJ | - |
dc.contributor.author | Lee, YH | - |
dc.contributor.author | Kim, KR | - |
dc.contributor.author | Park, CS | - |
dc.date.accessioned | 2015-11-23T23:34:25Z | - |
dc.date.available | 2015-11-23T23:34:25Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 0003-9985 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/12021 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/12021 | - |
dc.description.abstract | CONTEXT:
The ability of intermediate trophoblasts to invade maternal tissue during placentation depends on how well they can degrade the extracellular matrix. Invasion into the extracellular matrix requires many complex proteases. A disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) is a novel family of secreted metalloproteinases. The ADAMTS-1, -4, -5, and -14 subtypes are known to be expressed in human placenta, but little is understood about their expression patterns. OBJECTIVE: To examine the expression patterns of ADAMTS-1, -4, -5, and -14 in specific human placenta cell types during gestation and in gestational trophoblastic diseases. DESIGN: Placental tissues were obtained from 25 pregnant women and 21 cases of gestational trophoblastic diseases (10 early complete moles, 3 placental site trophoblastic tumors, 4 invasive moles, and 4 choriocarcinomas). The expression of the 4 ADAMTS was analyzed by immunohistochemistry. RESULTS: ADAMTS-1, -4, -5, and -14 were differentially expressed by the human placenta throughout gestation in a time-specific and cell type-specific manner, as well as in gestational trophoblastic diseases. ADAMTS-1 showed gradually strong staining intensity in gestational trophoblastic diseases according to the invasive potential but showed consistent strong intensity throughout normal placenta. ADAMTS-4 and ADAMTS-5 exhibited higher and restricted expression in first-trimester intermediate trophoblasts. They also exhibited comparably strong expression in gestational trophoblastic diseases. However, ADAMTS-14 expression remained unchanged throughout gestation. CONCLUSIONS: The restricted expression pattern of ADAMTS-4 and ADAMTS-5 and their increased expression in gestational trophoblastic diseases suggest that these 2 ADAMTS subtypes are associated with a biological phenotype of trophoblasts involved in human placentation and the development of gestational trophoblastic diseases. | - |
dc.language.iso | en | - |
dc.subject.MESH | ADAM Proteins | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Choriocarcinoma | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Gene Expression Regulation | - |
dc.subject.MESH | Gene Expression Regulation, Neoplastic | - |
dc.subject.MESH | Gestational Trophoblastic Disease | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hydatidiform Mole, Invasive | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Placenta | - |
dc.subject.MESH | Pregnancy | - |
dc.subject.MESH | Procollagen N-Endopeptidase | - |
dc.subject.MESH | Uterine Neoplasms | - |
dc.title | Differential expression patterns of a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS) -1, -4, -5, and -14 in human placenta and gestational trophoblastic diseases. | - |
dc.type | Article | - |
dc.identifier.pmid | 24786121 | - |
dc.contributor.affiliatedAuthor | 이, 용희 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.5858/arpa.2012-0227-OA | - |
dc.citation.title | Archives of pathology & laboratory medicine | - |
dc.citation.volume | 138 | - |
dc.citation.number | 5 | - |
dc.citation.date | 2014 | - |
dc.citation.startPage | 643 | - |
dc.citation.endPage | 650 | - |
dc.identifier.bibliographicCitation | Archives of pathology & laboratory medicine, 138(5). : 643-650, 2014 | - |
dc.identifier.eissn | 1543-2165 | - |
dc.relation.journalid | J000039985 | - |
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