Molecular genetics, therapeutics and RET inhibitor resistance for medullary thyroid carcinoma and future perspectives.

IF 8.2 2区 生物学 Q1 CELL BIOLOGY Cell Communication and Signaling Pub Date : 2024-09-28 DOI:10.1186/s12964-024-01837-x
Ying Zhang, Wei-Hui Zheng, Shi-Hong Zhou, Jia-Lei Gu, Qing Yu, Yi-Zhou Zhu, Yu-Jie Yan, Zhi Zhu, Jin-Biao Shang
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Abstract

Medullary thyroid carcinoma (MTC) is a rare type of thyroid malignancy that accounts for approximately 1-2% of all thyroid cancers (TCs). MTC include hereditary and sporadic cases, the former derived from a germline mutation of rearrangement during transfection (RET) proto-oncogene, whereas somatic RET mutations are frequently present in the latter. Surgery is the standard treatment for early stage MTC, and the 10-year survival rate of early MTC is over 80%. While for metastatic MTC, chemotherapy showing low response rate, and there was a lack of effective systemic therapies in the past. Due to the high risk (ca. 15-20%) of distant metastasis and limited systemic therapies, the 10-year survival rate of patients with advanced MTC was only 10-40% from the time of first metastasis. Over the past decade, targeted therapy for RET has developed rapidly, bringing hopes to patients with advanced and progressive MTC. Two multi-kinase inhibitors (MKIs) including Cabozantinib and Vandetanib have been shown to increase progression-free survival (PFS) for patients with metastatic MTC and have been approved as choices of first-line treatment. However, these MKIs have not prolonged overall survival (OS) and their utility is limited due to high rates of off-target toxicities. Recently, new generation TKIs, including Selpercatinib and Pralsetinib, have demonstrated highly selective efficacy against RET and more favorable side effect profiles, and gained approval as second-line treatment options. Despite the ongoing development of RET inhibitors, the management of advanced and progressive MTC remains challenging, drug resistance remains the main reason for treatment failure, and the mechanisms are still unclear. Besides, new promising therapeutic approaches, such as novel drug combinations and next generation RET inhibitors are under development. Herein, we overview the pathogenesis, molecular genetics and current management approaches of MTC, and focus on the recent advances of RET inhibitors, summarize the current situation and unmet needs of these RET inhibitors in MTC, and provide an overview of novel strategies for optimizing therapeutic effects.

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甲状腺髓样癌的分子遗传学、疗法和RET抑制剂耐药性及未来展望。
甲状腺髓样癌是一种罕见的甲状腺恶性肿瘤,约占所有甲状腺癌(TC)的1-2%。甲状腺髓样癌包括遗传性和散发性病例,前者源于转染过程中重排(RET)原癌基因的种系突变,而后者则经常出现体细胞RET突变。手术是治疗早期 MTC 的标准方法,早期 MTC 的 10 年生存率超过 80%。而对于转移性 MTC,化疗的反应率较低,过去一直缺乏有效的系统疗法。由于远处转移风险高(约 15%-20%)和系统疗法有限,晚期 MTC 患者自首次转移起的 10 年生存率仅为 10%-40%。近十年来,RET 靶向治疗发展迅速,为晚期和进展期 MTC 患者带来了希望。包括卡博替尼(Cabozantinib)和凡德他尼(Vandetanib)在内的两种多激酶抑制剂(MKIs)已被证明可提高转移性MTC患者的无进展生存期(PFS),并被批准作为一线治疗的选择。然而,这些 MKIs 并未延长总生存期(OS),而且由于脱靶毒性较高,其作用受到了限制。最近,包括赛乐替尼(Selpercatinib)和普拉西替尼(Pralsetinib)在内的新一代TKIs显示出对RET的高选择性疗效和更有利的副作用,并被批准作为二线治疗选择。尽管RET抑制剂的开发仍在继续,但晚期和进展期MTC的治疗仍然充满挑战,耐药仍是治疗失败的主要原因,其机制也仍不清楚。此外,新的治疗方法,如新型药物组合和新一代 RET 抑制剂正在开发中。在此,我们概述了 MTC 的发病机制、分子遗传学和目前的治疗方法,并重点介绍了 RET 抑制剂的最新进展,总结了这些 RET 抑制剂在 MTC 中的应用现状和尚未满足的需求,并概述了优化治疗效果的新策略。
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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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