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甘油磷脂驱动的脂质代谢重编程作为人类原发性肝细胞癌和胆管癌进展中的共同关键机制。

Glycerophospholipid-driven lipid metabolic reprogramming as a common key mechanism in the progression of human primary hepatocellular carcinoma and cholangiocarcinoma.

作者信息

Bi Yanran, Ying Xihui, Chen Wanbin, Wu Jiahao, Kong Chunli, Hu Weiming, Fang Shiji, Yu Junchao, Zhai Mengqian, Jiang Chengli, Chen Minjiang, Shen Lin, Ji Jiansong, Tu Jianfei

机构信息

Key Laboratory of Imaging Diagnosis and Minimally Invasive Intervention Research, Imaging Diagnostic and Interventional Minimally Invasive Institute, The Fifth Affiliated Hospital of Wenzhou Medical University, No 289, Kuocang Road, Lishui, 323000, China.

Clinical College of The Affiliated Central Hospital, School of Medcine, Lishui University, Lishui, 323000, China.

出版信息

Lipids Health Dis. 2024 Oct 1;23(1):326. doi: 10.1186/s12944-024-02298-4.

DOI:10.1186/s12944-024-02298-4
PMID:39354487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11443871/
Abstract

Metabolic reprogramming, a key mechanism regulating the growth and recurrence of hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA), still lacks effective clinical strategies for its integration into the precise screening of primary liver cancer. This study utilized ultra-high-performance liquid chromatography with quadrupole time-of-flight mass spectrometry to conduct a comprehensive, non-targeted metabolomics analysis, revealing significant upregulation of lipid metabolites such as phosphatidylcholine and lysophosphatidylcholine in patients with HCC and CCA, particularly within the glycerophospholipid metabolic pathway. Hematoxylin and eosin and immunohistochemical staining demonstrated marked upregulation of phospholipase A in tumor tissues, further emphasizing the potential of lipid metabolism as a therapeutic target and its important part in the course of cancer. This work provides a new viewpoint for addressing the clinical challenges associated with HCC and CCA, laying the groundwork for the broad application of early diagnosis and personalized treatment strategies, and ultimately aiming to provide tailored and precise therapeutic options for patients.

摘要

代谢重编程是调节肝细胞癌(HCC)和胆管癌(CCA)生长和复发的关键机制,但在将其整合到原发性肝癌的精确筛查中仍缺乏有效的临床策略。本研究利用超高效液相色谱与四极杆飞行时间质谱联用技术进行全面的非靶向代谢组学分析,发现HCC和CCA患者中磷脂酰胆碱和溶血磷脂酰胆碱等脂质代谢物显著上调,尤其是在甘油磷脂代谢途径中。苏木精和伊红染色及免疫组化染色显示肿瘤组织中磷脂酶A明显上调,进一步强调了脂质代谢作为治疗靶点的潜力及其在癌症进程中的重要作用。这项工作为应对与HCC和CCA相关的临床挑战提供了新的视角,为早期诊断和个性化治疗策略的广泛应用奠定了基础,最终旨在为患者提供量身定制的精准治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/305d3d926a8e/12944_2024_2298_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/d080a637c4fd/12944_2024_2298_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/aa5352a7330c/12944_2024_2298_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/b449a93305b2/12944_2024_2298_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/1f2ab5108d87/12944_2024_2298_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/305d3d926a8e/12944_2024_2298_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/d080a637c4fd/12944_2024_2298_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/aa5352a7330c/12944_2024_2298_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/b449a93305b2/12944_2024_2298_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/1f2ab5108d87/12944_2024_2298_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092a/11443871/305d3d926a8e/12944_2024_2298_Fig4_HTML.jpg

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