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CXCL1 promotes cell migration in hepatocellular carcinoma by regulating the miR-30b-5p/ICAM-1 axis.
Chen, Yi-Hsin; Chu, Chih-Chun; Wei, Augusta I-Chin; Liu, Ju-Fang; Lai, Hong-Shiee.
Affiliation
  • Chen YH; Division of Pediatric Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Chu CC; Department of Emergency Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Wei AI; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Liu JF; Division of Pediatric Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
  • Lai HS; School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, Taipei, Taiwan.
J Cancer ; 15(15): 5007-5019, 2024.
Article in En | MEDLINE | ID: mdl-39132161
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Cancer Year: 2024 Document type: Article Affiliation country: Taiwán Country of publication: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Cancer Year: 2024 Document type: Article Affiliation country: Taiwán Country of publication: Australia