Permatasari Lanny Indah, Afifah Nadiya Nurul, Ishmatullah Maryam Hasymia, Intania Ruri, Halimah Eli, Barliana Melisa Intan
Department of Biological Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran, Sumedang, Indonesia.
Department of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran, Sumedang, Indonesia.
Cancer Manag Res. 2025 Feb 27;17:383-395. doi: 10.2147/CMAR.S501420. eCollection 2025.
Non-small cell lung cancer (NSCLC) is the most common form of lung cancer, accounting for 85% of all cases, with a poor 5-year survival rate of less than 20%. The majority of NSCLC patients are diagnosed at an advanced stage, contributing to the low survival rate. Platinum-based chemotherapy, including cisplatin and carboplatin, remains the cornerstone of treatment for advanced NSCLC. However, DNA repair mechanisms often hinder treatment efficacy, notably Base Excision Repair (BER), mediated by the X-ray Repair Cross Complementing 1 (XRCC1) protein. This review aims to investigate the role of polymorphisms in platinum resistance, focusing on their impact on DNA repair efficiency. XRCC1's involvement in the BER pathway is critical for repairing DNA damage caused by platinum agents, and polymorphisms in have been linked to altered repair capacity, influencing clinical outcomes and resistance to platinum-based chemotherapy in NSCLC patients.
非小细胞肺癌(NSCLC)是肺癌最常见的形式,占所有病例的85%,5年生存率低至20%以下。大多数NSCLC患者在晚期被诊断出来,这导致了生存率较低。以铂类为基础的化疗,包括顺铂和卡铂,仍然是晚期NSCLC治疗的基石。然而,DNA修复机制常常阻碍治疗效果,尤其是由X射线修复交叉互补蛋白1(XRCC1)介导的碱基切除修复(BER)。本综述旨在研究多态性在铂耐药中的作用,重点关注它们对DNA修复效率的影响。XRCC1参与BER途径对于修复铂类药物引起的DNA损伤至关重要,其多态性与修复能力改变有关,影响NSCLC患者的临床结局和对铂类化疗的耐药性。