File Download
There are no files associated with this item.
Supplementary
-
Citations:
- Scopus: 0
- Appears in Collections:
Article: Clinical and pathological significance of the integrin α5β1 expression in endometrial adenocarcinoma
Title | Clinical and pathological significance of the integrin α5β1 expression in endometrial adenocarcinoma |
---|---|
Authors | |
Keywords | Endometrial Adenocarcinoma Immunohistochemistry Integrin Α5β1 |
Issue Date | 2001 |
Citation | Fudan University Journal of Medical Sciences, 2001, v. 28 n. 3, p. 251-253 How to Cite? |
Abstract | Purpose: To investigate the integrin α5β1 expression in endometrial adenocarcinoma and its relation with tumor differentiation, invasion, metastasis and prognosis. Methods: The integrin α5β1 expression was detected in 92 cases of endometrial adenocarcinoma by immunohistochemistry technique (PAP method). Results: The expression of integrin α5β1 in 77.1% cases with endometrial adenocarcinoma were weaker or loss. The positive rate of integrin α5β1 was lower in poorly differentiated carcinoma group than in well differentiated group (P < 0.05). The positive rate of integrin α5β1 was lower in lymph-node metastatic group than in nonmetastatic group (P < 0.05). The five-year survival rate of integrin α5β1 positive group was higher in integrin α5β1 positive group (78.4%) than that in negative group (19.2%, P< 0.05). Conclusions: The weak or loss expression of integrin α5β1 was correlated with differentiation and metastasis of endometrial adenocarcinoma. The expression of integrin α5β1 may have prognostic value. |
Persistent Identifier | http://hdl.handle.net/10722/90894 |
ISSN | 2023 SCImago Journal Rankings: 0.117 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, J | en_HK |
dc.contributor.author | Lin, B | en_HK |
dc.contributor.author | Zhang, X-R | en_HK |
dc.contributor.author | Gao, T | en_HK |
dc.contributor.author | Zhao, Z-H | en_HK |
dc.date.accessioned | 2010-09-17T10:09:58Z | - |
dc.date.available | 2010-09-17T10:09:58Z | - |
dc.date.issued | 2001 | en_HK |
dc.identifier.citation | Fudan University Journal of Medical Sciences, 2001, v. 28 n. 3, p. 251-253 | en_HK |
dc.identifier.issn | 1672-8467 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/90894 | - |
dc.description.abstract | Purpose: To investigate the integrin α5β1 expression in endometrial adenocarcinoma and its relation with tumor differentiation, invasion, metastasis and prognosis. Methods: The integrin α5β1 expression was detected in 92 cases of endometrial adenocarcinoma by immunohistochemistry technique (PAP method). Results: The expression of integrin α5β1 in 77.1% cases with endometrial adenocarcinoma were weaker or loss. The positive rate of integrin α5β1 was lower in poorly differentiated carcinoma group than in well differentiated group (P < 0.05). The positive rate of integrin α5β1 was lower in lymph-node metastatic group than in nonmetastatic group (P < 0.05). The five-year survival rate of integrin α5β1 positive group was higher in integrin α5β1 positive group (78.4%) than that in negative group (19.2%, P< 0.05). Conclusions: The weak or loss expression of integrin α5β1 was correlated with differentiation and metastasis of endometrial adenocarcinoma. The expression of integrin α5β1 may have prognostic value. | en_HK |
dc.language | eng | en_HK |
dc.relation.ispartof | Fudan University Journal of Medical Sciences | en_HK |
dc.subject | Endometrial Adenocarcinoma | en_HK |
dc.subject | Immunohistochemistry | en_HK |
dc.subject | Integrin Α5β1 | en_HK |
dc.title | Clinical and pathological significance of the integrin α5β1 expression in endometrial adenocarcinoma | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Lin, B:blin@hku.hk | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.scopus | eid_2-s2.0-0042823480 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0042823480&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 28 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 251 | en_HK |
dc.identifier.epage | 253 | en_HK |
dc.identifier.issnl | 1672-8467 | - |