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通过SLC27A1进行的长链脂肪酸转运增强二酰甘油-3-磷酸合成并加速结直肠癌转移。

Long chain fatty acid transport via SLC27A1 enhances DAG-3-P synthesis and accelerates colorectal cancer metastasis.

作者信息

Tong Kuiyuan, Yang Chao, Cai Lizheng, Yang Wanli, Yu Ruihua, Xu Juan, Jiang Feng

机构信息

Translational Institute for Cancer Pain, Chongming Hospital Affiliated to Shanghai University of Health & Medicine Sciences (Xinhua Hospital Chongming Branch), Shanghai, 202150, China.

Songjiang Institute of Shanghai Jiao Tong University School of Medicine, Shanghai, 201602, China.

出版信息

Sci Rep. 2025 Aug 29;15(1):31937. doi: 10.1038/s41598-025-17143-6.

Abstract

Colorectal cancer (CRC) is a major global health issue. Despite advancements in treatment, CRC patients still face challenges of metastasis and variable prognosis. Circulating tumor cells (CTCs) shed from the primary tumor into the peripheral blood circulation provide new insights into the potential molecular mechanisms driving tumor progression and metastasis.In this study, we comprehensively analyzed CTC data, primary tumor tissue data, and metastatic tumor tissue data from CRC patients to identify pathways associated with CRC metastasis, with a specific focus on the transport processes of vitamins, nucleosides, and related molecules. Using machine learning techniques, we identified Solute Carrier Family 27 Member 1 (SLC27A1) as the biomarker most closely associated with CRC metastasis. SLC27A1 is responsible for transporting extracellular long-chain fatty acids (LCFAs) into cells, and the model constructed based on the expression level of this gene achieved an accuracy of over 95% in assisting the assessment of patients' metastatic risk across different datasets.Further studies revealed that the process of intracellular LCFAs being catalyzed to synthesize diacylglycerol-3-phosphate (DAG-3P) is closely related to CRC metastasis. Laboratory experiments confirmed that downregulation of SLC27A1 expression in colorectal cancer cell lines (Caco-2 and T84) significantly inhibited cell migration and invasion abilities, directly validating the functional role of this gene in promoting tumor metastasis. Additionally, statistical analysis using data from the National Health and Nutrition Examination Survey database (2017-2020) showed a slightly higher incidence of cancer in populations with high-fat intake.These findings, integrating computational predictions and experimental validation, deepen our understanding of the biological mechanisms of colorectal cancer and provide potential targets for therapeutic interventions and personalized treatment strategies.

摘要

结直肠癌(CRC)是一个重大的全球健康问题。尽管治疗方面取得了进展,但CRC患者仍面临转移和预后差异的挑战。从原发性肿瘤脱落进入外周血液循环的循环肿瘤细胞(CTC)为驱动肿瘤进展和转移的潜在分子机制提供了新的见解。在本研究中,我们全面分析了CRC患者的CTC数据、原发性肿瘤组织数据和转移性肿瘤组织数据,以确定与CRC转移相关的途径,特别关注维生素、核苷和相关分子的转运过程。使用机器学习技术,我们确定溶质载体家族27成员1(SLC27A1)是与CRC转移最密切相关的生物标志物。SLC27A1负责将细胞外长链脂肪酸(LCFA)转运到细胞内,基于该基因表达水平构建的模型在协助评估不同数据集中患者的转移风险方面达到了95%以上的准确率。进一步的研究表明,细胞内LCFA被催化合成二酰甘油-3-磷酸(DAG-3P)的过程与CRC转移密切相关。实验室实验证实,结肠癌细胞系(Caco-2和T84)中SLC27A1表达的下调显著抑制了细胞迁移和侵袭能力,直接验证了该基因在促进肿瘤转移中的功能作用。此外,使用国家健康和营养检查调查数据库(2017 - 2020)的数据进行的统计分析显示,高脂肪摄入人群的癌症发病率略高。这些发现整合了计算预测和实验验证,加深了我们对结直肠癌生物学机制的理解,并为治疗干预和个性化治疗策略提供了潜在靶点。

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