中国实用外科杂志 ›› 2022, Vol. 42 ›› Issue (03): 344-348.DOI: 10.19538/j.cjps.issn1005-2208.2022.03.14

• 文献综述 • 上一篇    下一篇

琥珀酸脱氢酶缺陷型胃肠间质瘤研究进展

杨舒雅,叶颖江,高志冬   

  1. 北京大学人民医院胃肠外科 北京大学人民医院外科肿瘤研究室,北京100044
  • 出版日期:2022-03-01 发布日期:2022-03-04

  • Online:2022-03-01 Published:2022-03-04

摘要: 琥珀酸脱氢酶(SDH)缺陷型胃肠间质瘤(GIST)是一类没有KIT/PDGFRA突变的野生型GIST,以SDHB免疫组化阴性为特征。SDH缺陷导致细胞内琥珀酸堆积,后者作为促癌代谢物可引发多种表观遗传学和代谢改变,促进肿瘤发生发展。SDH缺陷型GIST发病年龄早,病变部位以胃为主,可合并发生副神经节瘤或肺软骨瘤。该型GIST以手术治疗为主,对靶向治疗反应欠佳,替莫唑胺等传统化疗药物可能对其有潜在疗效。SDH缺陷型GIST的发病机制及有效治疗方法等仍有待进一步探索。

关键词: 胃肠间质瘤, 琥珀酸脱氢酶

Abstract: Research progress of succinate dehydrogenase-deficient gastrointestinal stromal tumors        YANG Shu-ya,YE Ying-jiang,GAO Zhi-dong. Department of Gastroenterological Surgery, Laboratory of Surgical Oncology, Peking University People's Hospital, Beijing 100044, China
Corresponding author:GAO Zhi-dong, E-mail:gaozhidong@pkuph.edu.cn
Abstract    Succinate dehydrogenase(SDH)-deficient gastrointestinal stromal tumor(GIST)is a type of wild-type GIST without KIT/PDGFRA mutation,and it is characterized by negative SDHB immunohistochemistry.SDH deficiency leads to the accumulation of succinic acid in cells.The latter,as a kind of oncometabolite,can trigger a variety of epigenetic and metabolic changes,thus promoting tumor occurrence and development.The age of onset of SDH-deficient GIST is often early,and the lesion is mainly located in the stomach,which sometimes can be associated with paraganglioma and/or pulmonary chondroma.This type of GIST is still primarily treated with surgery.It does not respond well to targeted drugs therapy,while traditional chemotherapy drugs such as temozolomide may potentially affect it. SDH-deficient GIST's pathogenesis and effective treatment methods need to be further explored.

Key words: gastrointestinal stromal tumor, succinate dehydrogenase