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p16 is a major inactivation target in hepatocellular carcinoma

Authors
 Myung Jin Baek  ;  Zhe Piao  ;  Nam-Gyun Kim  ;  Chanil Park  ;  Eui-Cheol Shin  ;  Jeon-Han Park  ;  Hee-Jung Jung  ;  Chul Geun Kim  ;  Hoguen Kim 
Citation
 Cancer, Vol.89(1) : 60-68, 2000 
Journal Title
 Cancer 
ISSN
 0008-543X 
Issue Date
2000
MeSH
Carcinoma, Hepatocellular/genetics* ; Cell Cycle Proteins* ; Cell Transformation, Neoplastic ; Cyclin-Dependent Kinase Inhibitor p15 ; Cyclin-Dependent Kinase Inhibitor p16/genetics ; DNA, Neoplasm/genetics ; Gene Deletion ; Genes, p16/genetics* ; Humans ; Liver Neoplasms/genetics* ; Methylation ; Promoter Regions, Genetic/genetics* ; Proteins/genetics ; RNA/genetics ; Transcription Factors/genetics ; Tumor Suppressor Protein p14ARF ; Tumor Suppressor Proteins*
Keywords
p16INK4A ; p15INK4B ; p14ARF ; homozygous deletions ; methylation inacti-vation
Abstract
BACKGROUND: The p16(INK4A) gene encodes 2 cell cycle regulator proteins, p16 and p14(ARF), by alternative splicing. This genetic locus also contains another cell cycle regulator gene, p15(INK4B), which encodes p15. The inactivation of the p16 protein has been demonstrated in some hepatocellular carcinomas (HCCs); however, the inactivation of the other 2 cell regulator proteins and their inactivation patterns are not well characterized. METHODS: To characterize the role of the above 3 cell cycle regulator proteins in HCCs, the authors examined the genomic status of the p16(INK4A) and p15(INK4B) genes and their RNA products in 20 HCC tissues and 7 human HCC cell lines. Homozygous deletions in each exon of p16(INK4A) and p15(INK4B) were evaluated by comparative multiplex polymerase chain reaction (PCR), and the methylation status of the p16(INK4A) and p15(INK4B) promoter region was analyzed by methylation specific PCR. RESULTS: Homozygous deletions were found in 6 of 20 HCCs (30%) and 2 of 7 HCC cell lines (29%). In 20 HCCs, the frequency of homozygous deletions was 20% in exon 1 of p15(INK4B), 20% in exon 2 of p15(INK4B), 10% in exon 1beta of p16(INK4A), 25% in exon 1alpha of p16(INK4A), 15% in exon 2 of p16(INK4A), and 15% in exon 3 of p16(INK4A). The authors found hypermethylation of the p16(INK4A) promoter region in 7 HCCs (35%) and 3 HCC cell lines (43%). The overall frequency of p16 alterations in HCCs, including hypermethylation and homozygous deletions, was 60% (12 of 20 cases). According to reverse transcriptase-PCR analysis, the absence of RNA expression was most frequent in p16 (11 of 20 cases, 55%) and less frequent in p15 (7 of 20 cases, 35%) and p14(ARF) (5 of 20 cases, 25%). CONCLUSIONS: Among the 3 cell cycle regulator proteins encoded at the 9p21 genetic locus, inactivation of p16 is the most frequent event in HCCs in which promoter hypermethylation and homozygous deletions are the common mechanisms.
Full Text
https://onlinelibrary.wiley.com/doi/full/10.1002/1097-0142%2820000701%2989%3A1%3C60%3A%3AAID-CNCR9%3E3.0.CO%3B2-3
DOI
10.1002/1097-0142(20000701)89:1<60::AID-CNCR9>3.0.CO;2-3
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers
Yonsei Authors
Kim, Ho Keun(김호근)
Park, Jeon Han(박전한) ORCID logo https://orcid.org/0000-0001-9604-3205
Park, Chan Il(박찬일)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/171584
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