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

作者信息

Lee J Y, 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

机构信息

Department of Pathology and Cancer Research Institute, Catholic University Medical College, Seoul, Korea.

出版信息

Cancer Res. 1998 Mar 15;58(6):1140-3.

PMID:9515797
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.

摘要

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