School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
Medical Oncology Unit, Fondazione Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS) San Gerardo dei Tintori, 20900 Monza, Italy.
Int J Mol Sci. 2024 Oct 18;25(20):11214. doi: 10.3390/ijms252011214.
Non-small cell lung cancer (NSCLC) remains a disease with a poor prognosis despite the advances in therapies. NSCLC with actionable oncogenic alterations represent a subgroup of diseases for which tyrosine kinase inhibitors (TKIs) have shown relevant and robust impact on prognosis, both in early and advanced stages. While the introduction of powerful TKIs increases the ratio of potentially curable patients, the disease does develop resistance over time through either secondary mutations or bypass activating tracks. Therefore, new treatment strategies are being developed to either overcome this inevitable resistance or to prevent it, and proteolysis targeting chimera agents (PROTACs) are among them. They consist of two linked molecules that bind to a target protein and an E3 ubiquitin ligase that causes ubiquitination and degradation of proteins of interest. In this paper, we review the rationale for PROTAC therapy and the current development of PROTACs for oncogene-addicted lung cancer. Moreover, we critically analyze the strengths and limitations of this promising technique that may help pave the way for future perspectives.
非小细胞肺癌(NSCLC)尽管在治疗方面取得了进展,但预后仍然较差。具有可操作的致癌改变的 NSCLC 是一组疾病,对于这些疾病,酪氨酸激酶抑制剂(TKI)在早期和晚期均对预后产生了相关且显著的影响。虽然引入强大的 TKI 增加了潜在可治愈患者的比例,但随着时间的推移,疾病会通过二次突变或旁路激活途径产生耐药性。因此,正在开发新的治疗策略来克服这种不可避免的耐药性或预防耐药性,其中包括蛋白水解靶向嵌合体(PROTAC)。它们由两个连接的分子组成,一个与靶蛋白结合,另一个与 E3 泛素连接酶结合,导致靶蛋白的泛素化和降解。本文综述了 PROTAC 治疗的原理以及针对致癌基因依赖型肺癌的 PROTAC 的最新进展。此外,我们还批判性地分析了这项有前途的技术的优缺点,这可能有助于为未来的研究铺平道路。