Research progress on lung cancer stem cells in epidermal growth factor receptor–tyrosine kinase inhibitor targeted therapy resistance in lung adenocarcinoma

Hong Zhang, Yanbin Wang, Xianglin Yuan, Yanmei Zou, Hua Xiong
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Abstract

Lung cancer is the leading cause of cancer-related deaths globally. In recent years, with the widespread use of genetic testing, epidermal growth factor receptor–tyrosine kinase inhibitor (EGFR-TKI)–targeted drugs have been efficacious to patients with lung adenocarcinoma exhibiting EGFR mutations. However, resistance to treatment is inevitable and eventually leads to tumor progression, recurrence, and reduction in the overall treatment efficacy. Lung cancer stem cells play a crucial role in the development of resistance toward EGFR-TKI–targeted therapy for lung adenocarcinoma. Lung cancer stem cells possess self-renewal, multilineage differentiation, and unlimited proliferation capabilities, which efficiently contribute to tumor formation and ultimately lead to tumor recurrence and metastasis. In this study, we evaluated the origin, markers, stemness index, relevant classic studies, resistance mechanisms, related signaling pathways, and strategies for reversing lung cancer stem cell resistance to EGFR-TKIs to provide new insights on delaying or reducing resistance and to improve the treatment efficacy of patients with EGFR-mutated lung adenocarcinoma in the future.
表皮生长因子受体-酪氨酸激酶抑制剂靶向治疗肺腺癌耐药性中的肺癌干细胞研究进展
肺癌是全球癌症相关死亡的首要原因。近年来,随着基因检测的广泛应用,表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKI)靶向药物对表皮生长因子受体突变的肺腺癌患者产生了疗效。然而,耐药性是不可避免的,最终会导致肿瘤进展、复发和整体疗效下降。肺癌干细胞在肺腺癌表皮生长因子受体-TKI靶向治疗的耐药性发展过程中起着至关重要的作用。肺癌干细胞具有自我更新、多系分化和无限增殖能力,能有效促进肿瘤形成,并最终导致肿瘤复发和转移。本研究对肺癌干细胞的起源、标志物、干性指数、相关经典研究、耐药机制、相关信号通路以及逆转肺癌干细胞对EGFR-TKIs耐药的策略进行了评估,以期为延缓或降低耐药提供新的见解,并在未来提高EGFR突变肺腺癌患者的治疗效果。
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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