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Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma.

Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma. Research Abstract Details 

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  • Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma. Abstract Text:

    mi-yong yunMi-Yong Yun,sang bum kimSang Bum Kim,sunhoo parkSunhoo Park,chul ju hanChul Ju Han,young-hoon hanYoung-Hoon Han,sun hee yoonSun Hee Yoon,sang hoon kimSang Hoon Kim,chang-min kimChang-Min Kim,dong-wook choiDong-Wook Choi,myung-haing choMyung-Haing Cho,gil-hong parkGil-Hong Park,kee-ho leeKee-Ho Lee,mi-yong yunMi-Yong Yun,sang bum kimSang Bum Kim,sunhoo parkSunhoo Park,chul ju hanChul Ju Han,young-hoon hanYoung-Hoon Han,sun hee yoonSun Hee Yoon,sang hoon kimSang Hoon Kim,chang-min kimChang-Min Kim,dong-wook choiDong-Wook Choi,myung-haing choMyung-Haing Cho,gil-hong parkGil-Hong Park,kee-ho leeKee-Ho Lee,

    Failure of mitotic checkpoint machinery leads to the chromosomal missegregation and nuclear endoreduplication, thereby driving the emergence of aneuploidy and tetraploidy population. Although abnormal nuclear ploidy and the resulting impairment of mitotic checkpoint function are typical physiological event leading to human hepatocellular carcinoma, any mutational change of mitotic checkpoint regulators has not yet been discovered. Therefore, we investigated the mutation of p31(comet), a recently identified mitotic checkpoint regulator, in human hepatocellular carcinoma. Of 51 human hepatocellular carcinoma tissue and 6 cell lines tested, five samples exhibited nucleotide sequence variations dispersed on four sites within the entire coding sequence. Among these sites with sequence substitutions, three were found to be missense mutation accompanied with amino acid change but one was a silent mutation. Of these sequence substitutions, two were present in both tumor and non-tumor liver tissues, suggesting the possibility of polymorphism. The present findings indicate that p31(comet) does not have an impact on the formation of aneuploidy and tetraploidy found in human hepatocellular carcinoma.

    Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma. Publishing Authors By Initials

    my yunMY Yun,sb kimSB Kim,s parkS Park,cj hanCJ Han,yh hanYH Han,sh yoonSH Yoon,sh kimSH Kim,cm kimCM Kim,dw choiDW Choi,mh choMH Cho,gh parkGH Park,kh leeKH Lee,my yunMY Yun,sb kimSB Kim,s parkS Park,cj hanCJ Han,yh hanYH Han,sh yoonSH Yoon,sh kimSH Kim,cm kimCM Kim,dw choiDW Choi,mh choMH Cho,gh parkGH Park,kh leeKH Lee,

    For similar abstracts research abstracts see: abstracts research

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    Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Experimental & molecular medicine

    VOLUME: 39

    Page Numbers: 508-13

    Journal Abbreviation: Exp. Mol. Med.

    ISSN: 1226-3613

    DAY: 31

    MONTH: Aug

    YEAR: 2007

    Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma. Information

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    LANGUAGE: eng

    NlmUniqueID: 9607880

    Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma. Keywords Mesh Terms:

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    Grant and Affiliation Information for Mutation analysis of p31comet gene, a negative regulator of Mad2, in human hepatocellular carcinoma.

    AFFILIATION: Laboratory of Radiation Molecular Oncology, Division of Radiation Cancer Biology, Korea Institute of Radiological and Medical Sciences, Department of Biochemistry, College of Medicine, Korea University, Seoul 136-701, Korea.

    Country: Korea (South)

    Korea (South) Research PublicationKorea (South) Research Publication

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    MEDLINETA: Exp Mol Med

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