Low Levels of Microsatellite Instability at Simple Repeated Sequences Commonly Occur in Human Hepatocellular Carcinoma

被引:57
作者
Goumard, Claire [1 ]
Desbois-Mouthon, Christele [1 ]
Wendum, Dominique [1 ,2 ]
Calmel, Claire [1 ]
Merabtene, Fatiha [1 ,3 ]
Scatton, Olivier [1 ,4 ]
Praz, Francoise [1 ]
机构
[1] UPMC Univ Paris 06, INSERM, CNRS, Sorbonne Univ,CRSA, Paris, France
[2] Hop St Antoine, AP HP, Serv Anat Pathol, Paris, France
[3] Plateforme Histomorphol St Antoine, UMS 30, Paris, France
[4] Hop St Antoine, AP HP, Serv Chirurg Hepatobiliaire, Paris, France
关键词
Hepatocellular carcinoma; microsatellite instability; cirrhosis; inflammation; DNA MISMATCH REPAIR; COLORECTAL-CANCER CELLS; DISEASE-FREE SURVIVAL; MONONUCLEOTIDE REPEATS; LIVER-TRANSPLANTATION; GENOMIC INSTABILITY; REPLICATION ERROR; HEPATITIS; HETEROZYGOSITY; EXPRESSION;
D O I
10.21873/cgp.20043
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: The aim of this study was to assess the incidence of MSI in a large series of human hepatocellular carcinomas (HCC) with various etiologies. Materials and Methods: The MSI status was determined by polymerase chain reaction (PCR) using 5 mononucleotide and 13 CAn dinucleotide repeats. Results: None of the 122 HCC samples displayed an MSI-High phenotype, as defined by the presence of alterations at more than 30% of the microsatellite markers analyzed. Yet, limited microsatellite instability consisting in the insertion or deletion of a few repeat motifs was detected in 32 tumor samples (26.2%), regardless of the etiology of the underlying liver disease. MSI tended to be higher in patients with cirrhosis (p = 0.051), possibly reflecting an impact of the inflammatory context in this process. Conclusion: Based on a large series of HCC with various etiologies, our study allowed us to definitely conclude that MSI is not a hallmark of HCC.
引用
收藏
页码:329 / 339
页数:11
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