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柠檬酸盐促进肿瘤细胞中脂质生物合成和衰老以用于肿瘤治疗。

Citrate Promotes Excessive Lipid Biosynthesis and Senescence in Tumor Cells for Tumor Therapy.

机构信息

Department of Immunology, Key Laboratory of Medical Science and Laboratory Medicine of Jiangsu Province, School of Medicine, Jiangsu University, Zhenjiang, 212013, P. R. China.

Division of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, 63104, USA.

出版信息

Adv Sci (Weinh). 2022 Jan;9(1):e2101553. doi: 10.1002/advs.202101553. Epub 2021 Nov 7.

DOI:10.1002/advs.202101553
PMID:34747157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8728847/
Abstract

Metabolic disorder is one of the hallmarks of cancers, and reprogramming of metabolism is becoming a novel strategy for cancer treatment. Citrate is a key metabolite and critical metabolic regulator linking glycolysis and lipid metabolism in cellular energy homeostasis. Here it is reported that citrate treatment (both sodium citrate and citric acid) significantly suppresses tumor cell proliferation and growth in various tumor types. Mechanistically, citrate promotes excessive lipid biosynthesis and induces disruption of lipid metabolism in tumor cells, resulting in tumor cell senescence and growth inhibition. Furthermore, ATM-associated DNA damage response cooperates with MAPK and mTOR signaling pathways to control citrate-induced tumor cell growth arrest and senescence. In vivo studies further demonstrate that citrate administration dramatically inhibits tumor growth and progression in a colon cancer xenograft model. Importantly, citrate administration combined with the conventional chemotherapy drugs exhibits synergistic antitumor effects in vivo in the colon cancer models. These results clearly indicate that citrate can reprogram lipid metabolism and cell fate in cancer cells, and targeting citrate can be a promising therapeutic strategy for tumor treatment.

摘要

代谢紊乱是癌症的特征之一,代谢重编程正在成为癌症治疗的新策略。柠檬酸是一种关键代谢物和关键代谢调节剂,在细胞能量平衡中连接糖酵解和脂代谢。本文报道柠檬酸处理(柠檬酸钠和柠檬酸)显著抑制各种肿瘤类型的肿瘤细胞增殖和生长。从机制上讲,柠檬酸促进脂质生物合成过度,并诱导肿瘤细胞中脂代谢紊乱,导致肿瘤细胞衰老和生长抑制。此外,ATM 相关的 DNA 损伤反应与 MAPK 和 mTOR 信号通路合作,控制柠檬酸诱导的肿瘤细胞生长停滞和衰老。体内研究进一步证明,柠檬酸给药可显著抑制结肠癌异种移植模型中的肿瘤生长和进展。重要的是,柠檬酸给药与常规化疗药物联合在结肠癌模型中具有协同的抗肿瘤作用。这些结果清楚地表明,柠檬酸可以重塑肿瘤细胞中的脂代谢和细胞命运,靶向柠檬酸可能是肿瘤治疗的一种有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/8244e4ce5eef/ADVS-9-2101553-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/2fefb6969e79/ADVS-9-2101553-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/7f3d39ee4dd1/ADVS-9-2101553-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/8244e4ce5eef/ADVS-9-2101553-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/2fefb6969e79/ADVS-9-2101553-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/7d834f87d3a1/ADVS-9-2101553-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/944fe703efc7/ADVS-9-2101553-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6d/8728847/86755660b190/ADVS-9-2101553-g004.jpg
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