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SLC7A11在肝癌中的研究进展

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原发性肝癌因其易转移性、高复发性及耐药性导致患者预后较差,故寻找肝癌治疗的特异性分子靶标至关重要.SLC7A11是铁死亡的关键抑制因子,通过介导胱氨酸摄取促进谷胱甘肽合成,保护细胞免受氧化应激损伤.近期有文献报道了 SLC7A11在肝癌发生、发展,介入栓塞治疗,免疫治疗,放射治疗,靶向药物耐药等方面的生物学作用.本文对此作一综述,旨在为肝癌分子靶向治疗提供新的思路与方向.
Research progress of SLC7A11 in liver cancer
The prognosis of patients with primary liver cancer is poor due to its easy metastasis,high recurrence,and drug resistance,so it is cru-cial to find specific molecular targets for the treatment of liver cancer.SLC7A11 is a key inhibitor of ferroptosis,promoting glutathione synthesis by mediating cystine uptake and protecting cells from oxidative stress damage.Recently,the biological effects of SLC7A11 on the occurrence and de-velopment of liver cancer,interventional embolization therapy,immunotherapy,radiation therapy,and targeted drug resistance have been reported.This paper gives a summary of this problem,aiming to provide new ideas and directions for molecular targeted therapy of liver cancer.

SLC7A11Liver cancerFerroptosisResearch progress

郝定盈、朱山飞、毛本亮、苑伟、吴帆、王百林

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贵州医科大学临床医学院,贵州贵阳 550004

暨南大学附属广州红十字会医院普外科,广东广州 510220

SLC7A11 肝癌 铁死亡 研究进展

国家自然科学基金广东省自然科学基金面上项目

819744422020A1515010799

2024

中国医药导报
中国医学科学院

中国医药导报

CSTPCD
影响因子:1.759
ISSN:1673-7210
年,卷(期):2024.21(13)
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