PITPNC1调控肿瘤细胞脂质代谢与铁死亡的研究进展
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1.中南大学 湘雅医学院,湖南 长沙 410013;2.中南大学湘雅医院 医学科学研究中心,湖南 长沙 410008

作者简介:

张皓翔,中南大学湘雅医学院硕士研究生,主要从事消化道肿瘤基础方面的研究。

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Research progress of PITPNC1 in regulating Lipid metabolism and ferroptosis in cancer cells
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1.Xiangya School of Medicine, Central South University, Changsha 410013, China;2.Institute of Medical Sciences, Xiangya Hospital, Central South University, Changsha 410008, China

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    摘要:

    脂质代谢介导铁死亡在肿瘤发生发展过程中起至关重要的作用,已成为当前肿瘤研究领域热点和难点。目前肿瘤相关调控脂质代谢和铁死亡的关键调节分子仍然不是十分清楚。研究表明,磷脂酰肌醇转移蛋白(PITP)家族的成员磷脂酰肌醇转运蛋白细胞质1(PITPNC1)特异性结合并转移磷脂酰肌醇和磷脂酸,促进细胞膜脂质转运,介导脂质代谢。新近发现,PITPNC1是一种脂质代谢相关促癌基因,在乳腺癌、肝癌、胃癌、直肠癌、肺癌和胰腺癌中高表达,参与调控肿瘤细胞的生长、转移和侵袭过程。笔者就PITPNC1介导脂质代谢相关信号通路可能对肿瘤细胞铁死亡的调控机制进行综述,以期加深对肿瘤细胞铁死亡以及脂质代谢的认识,为肿瘤靶向治疗药物研发提供了新思路。

    Abstract:

    Lipid metabolism-mediated ferroptosis plays a crucial role in the initiation and progression of tumors, making it a focal point and challenge in current cancer research. The key regulatory molecules involved in controlling lipid metabolism and ferroptosis in tumors remain not fully understood. Studies have indicated that phosphatidylinositol transfer protein cytoplasmic 1 (PITPNC1), a member of the phosphatidylinositol transfer protein family, specifically binds and transfers phosphatidylinositol and phosphatidic acid, facilitating the transfer of lipids across cell membranes and mediating lipid metabolism. Recently, it has been found that PITPNC1 is a lipid metabolism-related oncogene, highly expressed in various cancers such as breast, liver, gastric, colorectal, lung, and pancreatic cancers, and participates in regulating the growth, migration, and invasion processes of tumor cells. Here, the authors provide a review of the potential regulatory mechanisms of PITPNC1-mediated lipid metabolism-related signaling pathways on ferroptosis in tumor cells, so as to deepen our understanding of tumor cell ferroptosis and lipid metabolism, offers new perspectives for the development of targeted therapies in cancer treatment.

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张皓翔,张赛. PITPNC1调控肿瘤细胞脂质代谢与铁死亡的研究进展[J].中国普通外科杂志,2024,33(1):131-137.
DOI:10.7659/j. issn.1005-6947.2024.01.015

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  • 收稿日期:2023-10-19
  • 最后修改日期:2023-12-27
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  • 在线发布日期: 2024-02-05