Cathelicidin Antimicrobial Peptide Acts as a Tumor Suppressor in Hepatocellular Carcinoma

• Published in: International journal of molecular sciences Vol. 24; no. 21; p. 15652
• Main Authors: Huang, Lien-Hung, Rau, Cheng-Shyuan, Liu, Yueh-Wei, Lin, Hui-Ping, Wu, Yi-Chan, Tsai, Chia-Wen, Chien, Peng-Chen, Wu, Chia-Jung, Huang, Chun-Ying, Hsieh, Ting-Min, Hsieh, Ching-Hua
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2023
• Subjects: Cancer; Cell cycle; Cell growth; Drug resistance; Enzymes; Health aspects; Hepatoma; Insulin-like growth factors; Liver cancer; Liver diseases; Medical prognosis; Oncology, Experimental; Peptides; Proteins; Proteomics; Scientific equipment and supplies industry; Von Willebrand factor; United States; Taiwan
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms242115652

Hepatocellular carcinoma (HCC) is associated with high rates of metastasis and recurrence, and is one of the most common causes of cancer-associated death worldwide. This study examined the protein changes within circulating exosomes in patients with HCC against those in healthy people using isobaric tags for a relative or absolute quantitation (iTRAQ)-based quantitative proteomics analysis. The protein levels of von Willebrand factor (VWF), cathelicidin antimicrobial peptide (CAMP), and proteasome subunit beta type-2 (PSMB2) were altered in HCC. The increased levels of VWF and PSMB2 but decreased CAMP levels in the serum of patients with HCC were validated by enzyme-linked immunosorbent assays. The level of CAMP (the only cathelicidin found in humans) also decreased in the circulating exosomes and buffy coat of the HCC patients. The serum with reduced levels of CAMP protein in the HCC patients increased the cell proliferation of Huh-7 cells; this effect was reduced following the addition of CAMP protein. The depletion of CAMP proteins in the serum of healthy people enhances the cell proliferation of Huh-7 cells. In addition, supplementation with synthetic CAMP reduces cell proliferation in a dose-dependent manner and significantly delays G1-S transition in Huh-7 cells. This implies that CAMP may act as a tumor suppressor in HCC.