非小细胞肺癌中的EGFR突变和酪氨酸激酶抑制剂(TKI):综述

P. Gaur, Gaurav Singh, S. Bhattacharya, S. Kant, Sarika Pandey, R. Pandey, Pooja Singh
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引用次数: 1

摘要

肺癌是全世界癌症相关死亡的最常见原因。表皮生长因子受体(EGFR)在调控肿瘤细胞增殖、侵袭、血管生成、转移和凋亡的信号通路中起级联作用。由于EGFR在NSCLC中经常过表达,且EGFR表达水平与预后不良相关。EGFR抑制剂已成为治疗非小细胞肺癌(NSCLC)的一种新方法。吉非替尼是首个获批用于晚期非小细胞肺癌治疗的分子靶向药物。它是一种高效的EGFR TK抑制剂(TKI),可选择性阻断与癌症生长有关的信号转导途径。关键词肺癌,EGFR, NSCLC,酪氨酸激酶抑制剂(TKI)简介肺癌是世界范围内最常见的癌症相关死亡原因。肺癌的定义是肺组织细胞生长不受控制,可能导致转移、浸润邻近组织和肺外浸润。大多数肺癌是肺癌,起源于上皮细胞[1]。在乳腺癌之后,女性中第二常见的癌症是肺癌。它也是妇女癌症相关死亡的第二大原因。尽管最近在晚期非小细胞肺癌(NSCLC)的治疗方面取得了进展,但治愈率仍然很低[3-4]。因此,需要对肺癌进行进一步的分子研究,以制定新的治疗策略,改善肺癌患者的预后。研究发现,非小细胞肺癌的激活和增殖受表皮生长因子受体(EGFR)亚家族的生长因子和受体调控。肺癌治疗的主要治疗选择是手术干预、铂基化疗和放疗,但在访问本文在线快速响应代码网站中对非小细胞肺癌的表皮生长因子受体(EGFR)突变进行了描述:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EGFR Mutation and Tyrosine-Kinase Inhibitors (TKI) in Non Small Cell Lung Cancer: An Overview
Lung cancer is the most common cause of cancer related mortality worldwide. The epidermal-growthfactor receptor (EGFR) cascades the signaling pathway that regulates tumor-cell proliferation, invasion, angiogenesis, metastasis, and apoptosis. Since EGFR is often over-expressed in NSCLC and the level of EGFR expression correlates with poor prognosis. EGFR inhibitors have been developed as a novel therapy for non-small-cell lung cancer (NSCLC). Gefitinib is the first molecular targeted agent approved for the treatment of advanced NSCLC. It is a highly effective EGFR TK inhibitor (TKI) selectively blocks the signal transduction pathways implicated in cancer growth. Key-wordsLung Cancer, EGFR, NSCLC, Tyrosine Kinase Inhibitor (TKI) INTRODUCTION Lung cancer is the most common cause of cancer related mortality worldwide. Lung cancer is defined as the uncontrolled cell growth of lung tissues which may lead to metastasis, invasion of adjacent tissue and infiltration beyond the lungs. Majority of lung cancers are carcinoma of the lung and are derived from epithelial cells [1] . After breast cancer, the second most common cancer present in women is lung cancer. It also constitutes the second leading cause of cancer-related deaths in women. [2] Despite recent advances in the management of advanced non-small-cell lung cancer (NSCLC), the cure rate remains still low [3-4] . Hence further molecular investigation of lung cancer is required for the development of the new treatment strategies to improve the prognosis of lung cancer patients. It has been found that the activation and proliferation of NSCLC is regulated by growth factors and receptors of the epidermal growth factor receptor (EGFR) subfamily. The principal available therapeutic options for the treatment of lung cancer were surgical intervention, platinum-based chemotherapy and radiotherapy but with the description of epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer in the Access this article online Quick Response Code Website:
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