SGT College of Pharmacy, Shree Guru Gobind Singh Tricentenary University, Gurugram, 122505, India.
Swami Keshvanand Institute of Pharmacy (SKIP), Raiser, Bikaner, 334803, India.
J Environ Pathol Toxicol Oncol. 2023;42(1):27-50. doi: 10.1615/JEnvironPatholToxicolOncol.2022042983.
Treatment of lung cancer with conventional therapies, which include radiation, surgery, and chemotherapy results in multiple undesirable adverse or side effects. The major clinical challenge in developing new drug therapies for lung cancer is resistance, which involves mutations and disturbance in various signaling pathways. Molecular abnormalities related to epidermal growth factor receptor (EGFR), v-Raf murine sarcoma viral oncogene homolog B1 (B-RAF) Kirsten rat sarcoma virus (KRAS) mutations, translocation of the anaplastic lymphoma kinase (ALK) gene, mesenchymal-epithelial transition factor (MET) amplification have been studied to overcome the resistance and to develop new therapies for non-small cell lung cancer (NSCLC). But, inevitable development of resistance presents limits the clinical benefits of various new drugs. Here, we review current progress in the development of molecularly targeted therapies, concerning six clinical biomarkers: EGFR, ALK, MET, ROS-1, KRAS, and B-RAF for NSCLC treatment.
常规疗法(包括放疗、手术和化疗)治疗肺癌会导致多种不良的副作用。在开发肺癌新药物疗法方面的主要临床挑战是耐药性,涉及多种信号通路的突变和紊乱。表皮生长因子受体(EGFR)、鼠肉瘤病毒致癌基因同源物 B1(B-RAF)、Kirsten 大鼠肉瘤病毒(KRAS)突变、间变性淋巴瘤激酶(ALK)基因易位、间充质-上皮转化因子(MET)扩增等与分子异常相关的研究,旨在克服耐药性并开发针对非小细胞肺癌(NSCLC)的新疗法。但是,各种新药物不可避免的耐药性发展限制了它们的临床获益。在这里,我们综述了针对非小细胞肺癌治疗的六个临床生物标志物:EGFR、ALK、MET、ROS-1、KRAS 和 B-RAF 的分子靶向治疗的最新进展。