Source:http://linkedlifedata.com/resource/pubmed/id/21569090
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
6
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| pubmed:dateCreated |
2011-5-16
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| pubmed:abstractText |
Mucosal and acral melanomas have demonstrated different genetic alterations and biological behavior compared with more common cutaneous melanomas. It was recently reported that gain-of-function KIT mutations and/or copy number increases are more common in mucosal and acral melanomas. Thus, we studied the frequency and pattern of KIT aberrations in mucosal and acral melanomas in Korea. We analyzed 97 patients who were pathologically confirmed with mucosal or acral melanoma between 1997 and 2010 at Samsung Medical Center. Of the 97 melanoma patients, 92 were screened for mutations in KIT exons 11, 13, 17, and 18, BRAF and NRAS genes. KIT copy number was assessed by quantitative, real-time PCR. Of the 97 patients, 55 (56.7%) were mucosal, 40 (41.2%) were acral melanoma, and two were of unknown primary origin. Among seven cases with KIT mutation, five (60.0%) occurred in exon 11, one (20.0%) in exon 17, and one (20.0%) in exon 13. Point mutations were the most common, resulting in substitutions in exon 11 (K558R, T574A, L576P, and V559A), exon 13 (N655K), and exon 17 (N822K). A novel Thr574Ala (c.1720A>G) KIT mutation, which has not been reported in melanoma or other tumor types, was identified in one genital melanoma case. Of the 97 mucosal or acral melanoma specimens, 49 were tested for KIT gene copy number changes using quantitative PCR. Increased KIT copy number was identified in 15 patients: seven (40%) of 20 acral melanomas and eight (31%) of 26 mucosal melanomas. Our study implicates that a significant proportion of acral and mucosal melanomas have KIT mutations in Asian population.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:month |
Jun
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| pubmed:issn |
1600-0463
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| pubmed:author | |
| pubmed:copyrightInfo |
© 2011 The Authors. APMIS © 2011 APMIS.
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| pubmed:issnType |
Electronic
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| pubmed:volume |
119
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
330-5
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| pubmed:meshHeading |
pubmed-meshheading:21569090-Adolescent,
pubmed-meshheading:21569090-Adult,
pubmed-meshheading:21569090-Aged,
pubmed-meshheading:21569090-Aged, 80 and over,
pubmed-meshheading:21569090-Asian Continental Ancestry Group,
pubmed-meshheading:21569090-DNA Mutational Analysis,
pubmed-meshheading:21569090-Exons,
pubmed-meshheading:21569090-Female,
pubmed-meshheading:21569090-Gene Dosage,
pubmed-meshheading:21569090-Humans,
pubmed-meshheading:21569090-Male,
pubmed-meshheading:21569090-Melanoma,
pubmed-meshheading:21569090-Middle Aged,
pubmed-meshheading:21569090-Mucous Membrane,
pubmed-meshheading:21569090-Mutation,
pubmed-meshheading:21569090-Polymerase Chain Reaction,
pubmed-meshheading:21569090-Proto-Oncogene Proteins B-raf,
pubmed-meshheading:21569090-Proto-Oncogene Proteins c-kit,
pubmed-meshheading:21569090-Republic of Korea,
pubmed-meshheading:21569090-Retrospective Studies,
pubmed-meshheading:21569090-Young Adult,
pubmed-meshheading:21569090-ras Proteins
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| pubmed:year |
2011
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| pubmed:articleTitle |
KIT amplification and gene mutations in acral/mucosal melanoma in Korea.
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| pubmed:affiliation |
Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
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| pubmed:publicationType |
Journal Article
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