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甲状腺未分化癌分子机制和治疗的研究进展

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甲状腺未分化癌(anaplastic thyroid carcinoma,ATC)是最具侵袭性的恶性肿瘤,预后极差.ATC发病机制复杂,目前尚无有效的治疗手段.近年来,随着对驱动ATC遗传(如BRAF V600E、TP53、TERT、PIK3CA突变等)和表观遗传(如组蛋白甲基化、组蛋白去乙酰化、microRNA调节通路等)改变的深入了解,分子靶向治疗为ATC患者带来新的希望.本文综述了ATC发病分子机制、靶向治疗和其他治疗的最新成果.
Research progress on molecular mechanism and treatment for anaplastic thyroid carcinoma
Anaplastic thyroid carcinoma(ATC)is the most aggressive malignancy with poor prognosis.The pathogenesis of ATC is complex,and there is no effective treatment at present.In recent years,with the deep understanding of the genetic(such as BRAF V600E,TP53,TERT,PIK3CA mutations,etc.)and epigenetic(such as histone methylation,histone deacetylation,microRNA regulatory pathways,etc.)changes driving ATC,molecular targeted therapy has brought new hope to ATC patients.This article reviews the molecular mechanisms of ATC and the latest achievements in targeted therapy and other therapies.

anaplastic thyroid cancergene mutationtargeted therapy

李尤、郭宏鹏、张艺彤、刘俊良、俞建华、张金辉、孙成林

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沈阳医学院附属中心医院普外科,辽宁 沈阳 110024

沈阳市苏家屯区中心医院普外科

甲状腺未分化癌 基因突变 靶向治疗

2024

沈阳医学院学报
沈阳医学院

沈阳医学院学报

影响因子:0.591
ISSN:1008-2344
年,卷(期):2024.26(3)