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PMID: 9515797 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix.

Cancer research ·Vol. 58 ·No. 6 ·1998-03-15 ·Pages 1140-3

Lee JY, Dong SM, Kim HS, Kim SY, Na EY, Shin MS, Lee SH, Park WS, Kim KM, Lee YS, Jang JJ, Yoo NJ

Abstract

Adenoma malignum (AM) is known to be one of the malignant tumors that is commonly associated with Peutz-Jeghers syndrome. Recently, the genetic locus of Peutz-Jeghers syndrome was mapped to the telomeric region of chromosome 19p. We analyzed nine sporadic cases of AM with high-density loss of heterozygosity to study the region of chromosome 19p13.2-13.3 using eight microsatellite markers. Our deletion mapping data revealed a distinct region with 100% loss of heterozygosity frequency at marker D19S216. This result indicates that a putative tumor suppressor gene for AM is located at D19S216 on chromosomal band 19p13.3 and plays an important role in AM tumorigenesis.

MeSH Terms
Adenocarcinoma/genetics Adenoma/genetics Cell Separation Chromosome Mapping Chromosomes, Human, Pair 19 Female Genes, Tumor Suppressor Humans Loss of Heterozygosity Peutz-Jeghers Syndrome/genetics Sequence Deletion Uterine Cervical Neoplasms/genetics
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Lee J Y
Department of Pathology and Cancer Research Institute, Catholic University Medical College, Seoul, Korea.
Dong S M
Kim H S
Kim S Y
Na E Y
Shin M S
Lee S H
Park W S
Kim K M
Lee Y S
Jang J J
Yoo N J
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1998-03-15
Pages
1140-3
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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