Identıfıcatıon of KRAS Mutatıons in Colorectal Carcınoma Patıents at Dr. M. Djamıl Hospıtal, West Sumatra-Indonesıa

R. Maliza, Hevi Horiza, S. Syukur, Allimuddin Tofrizal, Bramadi Arya
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Abstract

Kirsten rat sarcoma viral oncogene (KRAS) gene mutations lead to abnormal activation of the RAS signalling pathway and have been associated with poor prognosis and resistance to some therapeutics. This study aimed to identify mutation characteristics of the KRAS genes codon 12 and 13 in colorectal cancer patients in West Sumatra. KRAS mutations were analyzed in 20 DNA of colorectal cancer patients' tissue samples by using polymerase chain reaction (PCR) with specific primer and direct sequencing analysis. Our findings showed five samples (25%) with mutated KRAS at codons 12 and 13 (including three samples with GGT→GAT, one sample with GGT→GTT in codon 12, and one sample with GGC→GAC in codon 13). In conclusion, we found two variations of amino acid changes at codon 12 (G12D and G12V) and one at codon 13 (G13D). More research with many samples is required to obtain conclusive data on the relationship between these gene mutations and colorectal cancer response to therapy and prognosis.
大肠癌患者和M.Djamıl Hospıtal博士KRAS突变的鉴定,印度尼西亚西苏门答腊
Kirsten大鼠肉瘤病毒癌基因(KRAS)基因突变导致RAS信号通路的异常激活,并与不良预后和对某些治疗方法的耐药性有关。本研究旨在确定西苏门答腊癌症大肠癌患者KRAS基因密码子12和13的突变特征。采用特异性引物聚合酶链反应(PCR)和直接测序分析方法,对20例癌症大肠癌组织标本进行了KRAS突变分析。我们的研究结果显示,5个样本(25%)在密码子12和13处具有突变的KRAS(包括3个GGT样本→GAT,一个带有GGT的样品→密码子12中的GTT和一个GGC样本→密码子13中的GAC)。总之,我们在密码子12(G12D和G12V)和密码子13(G13D)发现了两种氨基酸变化。需要对许多样本进行更多的研究,以获得关于这些基因突变与癌症治疗反应和预后之间关系的结论性数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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