Source:http://linkedlifedata.com/resource/pubmed/id/11241409
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2001-3-12
|
pubmed:abstractText |
Deletions or mutations of the E-cadherin gene may result in reduced cell adhesiveness. In particular, conservative point mutations within the N-terminal calcium-binding pocket (including exons 7, 8, and 9) are frequently detected in several cancers and are enough to abolish cell-cell adhesion. There have been no studies on E-cadherin gene mutations in human intrahepatic cholangiocarcinoma (ICC). Human ICCs were therefore investigated for E-cadherin gene mutations within exons 7, 8, and 9. In addition, the relationships were analysed between their mutations and the immunohistochemical expression of E-cadherin, histological grade, and clinicopathological parameters. The E-cadherin gene was analysed in 34 tumours by nested polymerase chain reaction/single-strand conformation polymorphism (PCR/SSCP) followed by DNA sequencing. In four of the 34 cases (11.8%), tumour-restricted mobility shifts were observed; two cases harboured a single shift, one case presented two different mobility shifts, and one case presented three different mobility shifts within exons 7 and 8, encoding extracellular domains of E-cadherin. Polymorphism as previously reported was not identified and all seven new DNA alterations were not present in genomic DNA of non-tumour origin. The E-cadherin gene mutations correlated significantly with down-regulated E-cadherin protein expression and high ICC histological grade. These data suggest that E-cadherin gene mutations in ICC are associated with reduced cell adhesiveness and high histological grade.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0022-3417
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
193
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
310-7
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:11241409-Adult,
pubmed-meshheading:11241409-Aged,
pubmed-meshheading:11241409-Aged, 80 and over,
pubmed-meshheading:11241409-Bile Duct Neoplasms,
pubmed-meshheading:11241409-Bile Ducts, Intrahepatic,
pubmed-meshheading:11241409-Cadherins,
pubmed-meshheading:11241409-Cholangiocarcinoma,
pubmed-meshheading:11241409-Down-Regulation,
pubmed-meshheading:11241409-Female,
pubmed-meshheading:11241409-Humans,
pubmed-meshheading:11241409-Male,
pubmed-meshheading:11241409-Middle Aged,
pubmed-meshheading:11241409-Mutation,
pubmed-meshheading:11241409-Neoplasm Proteins,
pubmed-meshheading:11241409-Polymerase Chain Reaction,
pubmed-meshheading:11241409-Polymorphism, Single-Stranded Conformational
|
pubmed:year |
2001
|
pubmed:articleTitle |
E-cadherin gene mutations in human intrahepatic cholangiocarcinoma.
|
pubmed:affiliation |
Second Department of Pathology, Tottori University, Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Tottori, Japan.
|
pubmed:publicationType |
Journal Article
|