Loss of EGFR Mutation Expression Induced by NF1 Mutation in Non-Small Cell Lung Cancer: Non-Canonical Pathway of Tyrosine Kinase Inhibitors’ Resistance

Jose Gabriel Negron Rodriguez, Luis Orrego Poma, Manuel Leiva Gálvez, Maria Claudia Rodriguez Zavaleta, Wuilbert Rodriguez Pantigoso
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Abstract

Non-small cell lung carcinoma (NSCLC) is considered the first cause of cancer-related death worldwide and many therapies have been developed against the presence of actionable mutations. For example, targeting the EGFR mutation has changed the overall prognosis in NSCLC. However, resistance to treatment has emerged and many canonical mechanisms have already been described. NF1 mutation causes partial or total loss of function of neurofibromin, which activates several intracellular pathways (MAPK / ERK, PI3K / AKT, TGF -β / Smad), producing cellular proliferation, migration, apoptosis resistance and genetic instability, leading to loss of EGFR expression. Herein, we describe a case of a novel activation of a non-canonical pathway that led to treatment resistance by NF1 mutation.
非小细胞肺癌中NF1突变诱导的EGFR突变表达缺失:酪氨酸激酶抑制剂耐药的非典型途径
非小细胞肺癌(NSCLC)被认为是世界范围内癌症相关死亡的第一原因,许多针对可操作突变的治疗方法已经开发出来。例如,靶向EGFR突变已经改变了NSCLC的总体预后。然而,对治疗的耐药性已经出现,许多规范的机制已经被描述。NF1突变导致神经纤维蛋白部分或全部功能丧失,激活细胞内多条通路(MAPK / ERK、PI3K / AKT、TGF -β / Smad),产生细胞增殖、迁移、抗凋亡和遗传不稳定,导致EGFR表达丧失。在这里,我们描述了一个非规范途径的新激活,导致NF1突变的治疗抗性的情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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