[Research progress in non-small cell lung cancer with concomitant EML4-ALK fusion gene and EGFR gene mutation]

Zhongguo Fei Ai Za Zhi. 2011 Nov;14(11):880-4. doi: 10.3779/j.issn.1009-3419.2011.11.09.
[Article in Chinese]

Abstract

Lung cancer is one of the most prevalence malignances, of which non-small cell lung cancer (NSCLC) account for 80%-85% of lung cancer. Molecular target therapy is one of the most popular and promising field of NSCLC treatment, and its hotspots includes EGFR (epidermal growth factor receptor), EML4-ALK (echinoderm microtubule associated protein like4-anaplastic lymphoma kinase), etc. Former researches indicated that EML4-ALK fusion and EGFR mutation were excluded mutually. However, cases of patients harbored concomitant EML4-ALK fusion gene and EGFR mutation have been reported continuously at recent. This review aims to summarize the incidence and molecular structure of EML4-ALK fusion gene and EGFR mutation, as well as clinical features of patients with the concomitant genes induced NSCLC.

肺癌是最常见的恶性肿瘤之一,其中非小细胞肺癌(non-small cell lung cancer, NSCLC)占肺癌的80%-85%。分子靶向治疗是目前NSCLC最热门也是最具前景的领域之一,其中的热点分子包括表皮生长因子受体(epidermal growth factor receptor, EGFR)、棘皮动物微管样蛋白4-间变淋巴瘤激酶(echinoderm microtubule associated protein like4-anaplastic lymphoma kinase, EML4-ALK)等。既往研究认为EML4-ALK融合基因与EGFR突变不能共存。近期陆续报道了EML4-ALK融合基因与EGFR突变共存的病例。本文就EML4-ALK融合基因及EGFR突变基因的分子结构、发生率和目前已报道双突变患者的临床特点等进行综述。

Publication types

  • Review

MeSH terms

  • Biomedical Research
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Non-Small-Cell Lung / metabolism
  • ErbB Receptors / genetics*
  • ErbB Receptors / metabolism
  • Humans
  • Lung Neoplasms / genetics*
  • Mutation*
  • Oncogene Proteins, Fusion / genetics*
  • Oncogene Proteins, Fusion / metabolism

Substances

  • EML4-ALK fusion protein, human
  • Oncogene Proteins, Fusion
  • EGFR protein, human
  • ErbB Receptors