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CXCL1通过调节miR-30b-5p/ICAM-1轴促进肝细胞癌中的细胞迁移。

CXCL1 promotes cell migration in hepatocellular carcinoma by regulating the miR-30b-5p/ICAM-1 axis.

作者信息

Chen Yi-Hsin, Chu Chih-Chun, Wei Augusta I-Chin, Liu Ju-Fang, Lai Hong-Shiee

机构信息

Division of Pediatric Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

Department of Emergency Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

出版信息

J Cancer. 2024 Jul 22;15(15):5007-5019. doi: 10.7150/jca.95816. eCollection 2024.

Abstract

Hepatocellular carcinoma (HCC) is a highly lethal cancer with a growing global incidence and is often associated with poor prognosis due to its tendency to metastasize. Intercellular adhesion molecule (ICAM) 1 is a transmembrane protein found in various cancer cells and is associated with the spread of cancer and poor prognosis. Chemokine (C-X-C motif) ligand 1 (CXCL1) is a chemokine that significantly affects the cell motility of various cancers. However, the role of CXCL1 in ICAM-1 expression and in metastasis of hepatocellular carcinoma remains unclear. We determined that CXCL1 expression is positively and significantly associated with advanced-stage tumors in the HCC tissue array. Kaplan-Meier analysis revealed worse overall survival rates in the high CXCL1 expression group, suggesting its potential as a biomarker for cancer progression and stimulating hepatocellular carcinoma cells with CXCL1 enhanced migration abilities by upregulating ICAM-1 expression. CXCL1 was shown to enhance ICAM-1-dependent cell motility by inhibiting miR-30b-5p. This study provides novel evidence that CXCL1 could serve as a therapeutic target for metastasis in hepatocellular carcinoma.

摘要

肝细胞癌(HCC)是一种致死率很高的癌症,在全球的发病率不断上升,由于其易于转移,往往预后较差。细胞间黏附分子(ICAM)1是一种存在于多种癌细胞中的跨膜蛋白,与癌症扩散和预后不良有关。趋化因子(C-X-C基序)配体1(CXCL1)是一种对多种癌症的细胞运动有显著影响的趋化因子。然而,CXCL1在ICAM-1表达及肝细胞癌转移中的作用仍不清楚。我们确定在HCC组织阵列中,CXCL1表达与晚期肿瘤呈显著正相关。Kaplan-Meier分析显示,CXCL1高表达组的总生存率较差,这表明其有可能作为癌症进展的生物标志物,并且通过上调ICAM-1表达,用CXCL1刺激肝细胞癌细胞可增强其迁移能力。研究表明,CXCL1通过抑制miR-30b-5p来增强ICAM-1依赖的细胞运动。本研究提供了新的证据,表明CXCL1可作为肝细胞癌转移的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6495/11310878/536c286b5e54/jcav15p5007g001.jpg

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