Lipid reprogramming and ferroptosis crosstalk in clear cell renal cell carcinoma: metabolic vulnerabilities and therapeutic targeting

IF 33.9 1区医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY

Molecular Cancer Pub Date : 2025-10-02 DOI:10.1186/s12943-025-02457-w

Qing Deng, Yu Ji, Jian Liu, Tao Wen

引用次数: 0

Abstract

Clear cell renal cell carcinoma (ccRCC) features metabolic dysregulation, with altered lipid metabolism and ferroptosis dysregulation driving malignancy. This review examines the interplay between lipid reprogramming and ferroptosis resistance in ccRCC pathogenesis and therapy. Tumor cells exploit lipid accumulation for growth and evade ferroptosis adaptively. Preclinical studies show targeting lipid metabolism or inducing ferroptosis synergizes with anti-angiogenic/immunotherapy, improving survival. This study provides a framework for dual therapeutic strategies.

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透明细胞肾细胞癌中的脂质重编程和铁下垂串扰：代谢脆弱性和治疗靶向

透明细胞肾细胞癌（ccRCC）以代谢失调为特征，脂质代谢改变和铁下垂失调驱动恶性肿瘤。本文综述了脂质重编程与铁下沉抵抗在ccRCC发病机制和治疗中的相互作用。肿瘤细胞利用脂质积累生长并适应性地逃避铁下垂。临床前研究表明，靶向脂质代谢或诱导铁下垂与抗血管生成/免疫治疗协同作用，提高生存率。本研究为双重治疗策略提供了一个框架。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Molecular Cancer 医学-生化与分子生物学

CiteScore

54.90

自引率

2.70%

发文量

224

审稿时长

2 months

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