...
首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Associations Between Driver Gene Mutations and Cytotoxic Chemosensitivity in Patients with Non-small Cell Lung Cancer
【24h】

Associations Between Driver Gene Mutations and Cytotoxic Chemosensitivity in Patients with Non-small Cell Lung Cancer

机译:非小细胞肺癌患者司机基因突变与细胞毒性化学敏感性的关联

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background/Aim: Patients with non-small cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) gene mutations or echinoderm microtubule-associated protein-like 4 anaplastic lymphoma kinase (EML4-ALK) rearrangement often have a better prognosis when they are treated with specific inhibitors than when treated with cytotoxic agents. However, the associations between gene mutations and cytotoxic chemosensitivity are still unclear. The objective of the present study was to identify which clinicopathological factors, including genetic mutations, influence chemosensitivity, determined using the succinate dehydrogenase inhibition (SDI) test in patients with NSCLC. Materials and Methods: The chemosensitivity of tumor tissues from 96 patients with NSCLC who underwent surgical resection was evaluated using the SDI test. Results: In patients with adenocarcinoma, tumors with EGFR gene mutations were significantly more sensitive to 5-fluorouracil (5-FU) than tumors without EGFR gene mutations (p<0.0149). Conclusion: Our data suggest that patients with adenocarcinoma harboring EGFR gene mutations may be susceptible to 5-FU.
机译:背景/目的:非小细胞肺癌(NSCLC)患有表皮生长因子受体(EGFR)基因突变或海螺肽微管相关蛋白质样4Anpplastic淋巴瘤激酶(EML4-ALK)重排通常具有更好的预后用特异性抑制剂治疗,而不是用细胞毒性剂处理。然而,基因突变和细胞毒性化学敏感性之间的关联仍然不清楚。本研究的目的是鉴定哪些临床病理因素,包括遗传突变,影响使用NSCLC患者的琥珀酸脱氢酶抑制(SDI)试验确定的临床突变。材料和方法:使用SDI试验评估了96例接受手术切除的NSCLC患者的肿瘤组织的化学敏感性。结果:在腺癌患者中,患有EGFR基因突变的肿瘤对5-氟尿嘧啶(5-FU)的肿瘤显着比没有EGFR基因突变的肿瘤(P <0.0149)。结论:我们的数据表明,患有EGFR基因突变的腺癌患者可能易于5-FU。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号