[Study on point mutations of K-ras gene in non-small cell lung cancer in Guangxi]

Zhongguo Fei Ai Za Zhi. 2011 Jun;14(6):507-11. doi: 10.3779/j.issn.1009-3419.2011.06.06.
[Article in Chinese]

Abstract

Background and objective: Recent studies indicated that non-small cell lung cancer (NSCLC) patients with mutant K-ras were resistant to epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs). The aim of this study is to explore the relationship between the mutation of K-ras gene and NSCLC in Guangxi by detecting the point mutations in codon 12, 13 and 61 of K-ras gene in NSCLC.

Methods: The point mutations in codon 12, 13 and 61 of K-ras gene were detected by single-strand conformation polymorphism (SSCP) analysis of polymerase chain reaction (PCR) products and DNA sequencing analysis in 105 cases of NSCLC tissues and 30 cases of adjacent normal tissues.

Results: No point mutation in codon 12, 13 and 61 of K-ras gene was found in 105 cases of NSCLC tissues and 30 cases of adjacent normal tissues. In this study, the mutation frequency of K-ras gene in NSCLC was 0 (0/105).

Conclusion: The high proportion of K-ras gene in wild-type indicates that patients with NSCLC in Guangxi could take more benefits from the therapy with EGFR-TKIs.

背景与目的: 近期研究显示存在K-ras基因突变的非小细胞肺癌(non-small cell lung cancer, NSCLC)患者对表皮生长因子受体-酪氨酸激酶抑制剂(epidermal growth factor receptor-tyrosine kinase inhibitors, EGFR-TKIs)耐药。本研究检测广西地区NSCLC中K-ras基因密码子12、13及61点突变,旨在探讨K-ras基因突变与广西地区NSCLC的关系。

方法: 采用聚合酶链反应-单链构象多态性(polymerase chain reaction-single-strand conformation polymorphism, PCR-SSCP)分析法与PCR-DNA序列分析法联合检测105例新鲜NSCLC手术切除标本和30例癌旁正常肺组织中K-ras基因密码子12、13及61点突变。

结果: 105例NSCLC癌组织及30例癌旁正常肺组织中无1例发生K-ras基因点突变,本研究选取的NSCLC病例组的K-ras基因突变率为0(0/105)。

结论: 广西地区NSCLC中K-ras基因野生型的比例高,提示广西地区NSCLC患者更能从EGFR-TKIs治疗中获益。

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Asian People / genetics*
  • Base Sequence
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • China
  • Codon / genetics
  • DNA Mutational Analysis
  • Female
  • Genes, ras / genetics*
  • Humans
  • Lung Neoplasms / genetics*
  • Male
  • Middle Aged
  • Point Mutation / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Young Adult

Substances

  • Codon

Grants and funding

本研究受广西科学研究与技术开发计划项目(No.10124001A-44)和广西研究生教育创新计划项目(No.2010105981002M181)资助