Literature DB >> 15112348

C-kit gene mutation in human gastrointestinal stromal tumors.

Ying-Yong Hou1, Yun-Shan Tan, Meng-Hong Sun, Yong-Kun Wei, Jian-Fang Xu, Shao-Hua Lu, Su-Jie A-Ke-Su, Yan-Nan Zhou, Feng Gao, Ai-Hua Zheng, Tai-Ming Zhang, Wen-Zhong Hou, Jian Wang, Xiang Du, Xiong-Zeng Zhu.   

Abstract

AIM: To investigate the significance of c-kit gene mutation in gastrointestinal stromal tumors (GIST).
METHODS: Fifty two cases of GIST and 28 cases of other tumors were examined. DNA samples were extracted from paraffin sections and fresh blocks. Exons 11, 9 and 13 of the c-kit gene were amplified by PCR and sequenced.
RESULTS: Mutations of exon 11 were found in 14 of 25 malignant GISTs (56%), mutations of exon 11 of the c-kit gene were revealed in 2 of 19 borderline GISTs (10.5%), and no mutation was found in benign tumors. The mutation rate showed significant difference (chi2=14.39, P<0.01) between malignant and benign GISTs. Most of mutations consisted of the in-frame deletion or replication from 3 to 48 bp in heterozygous and homozygous fashions, None of the mutations disrupted the downstream reading frame of the gene. Point mutations and frame deletions were most frequently observed at codons 550-560, but duplications were most concentrated at codons 570-585. No mutations of exons 9 and 13 were revealed in GISTs, Neither c-kit gene expression nor gene mutations were found in 3 leiomyomas, 8 leiomyosarcomas, 2 schwannomas, 2 malignant peripheral nerve sheath tumors, 2 intra-abdominal fibromatoses, 2 malignant fibrous histiocytomas and 9 adenocarcinomas.
CONCLUSION: C-kit gene mutations occur preferentially in malignant GISTs and might be a clinically useful adjunct marker in the evaluation of GISTs and can help to differentiate GISTs from other mesenchymal tumors of gastrointestinal tract, such as smooth muscle tumors, schwannomas, etc.

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Year:  2004        PMID: 15112348      PMCID: PMC4622772          DOI: 10.3748/wjg.v10.i9.1310

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


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