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Article type: Research Article
Authors: Yu, Yong Minga; * | Hu, Yangb
Affiliations: [a] Department of Gastroenterology, Jiangxi Province Hospital of Integrated Chinese and Western Medicine, Nanchang, Jiangxi, China | [b] Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China
Correspondence: [*] Corresponding author: Yong Ming Yu, Department of Gastroenterology, Jiangxi Province Hospital of Integrated Chinese and Western Medicine, No. 90 Bayi Road, Xihu District, Nanchang, Jiangxi 330003, China. E-mail: yuyongmingyy@163.com.
Abstract: BACKGROUND: As a critical m6A RNA methylation regulator, HNRNPC has been revealed to serve as potential biomarkers in various human cancers. The specific expression and significance of HNRNPC in colorectal cancer remain unknown. OBJECTIVE: This study aimed to confirm HNRNPC expression level and evaluate its function in colorectal cancer progression. METHODS: 101 paired tissue samples were collected from colorectal cancer patients. HNRNPC levels in colorectal cancer were detected using PCR. CCK8 and transwell assays were conducted to estimate the effect of HNRNPC on cell growth and metastasis with the regulation of HNRNPC by cell transfection. RESULTS: Upregulated HNRNPC was observed in colorectal cancer compared with normal tissues and cells. The higher HNRNPC levels in tumor tissues were associated with the advanced TNM stage and positive lymph node metastasis. Meanwhile, HNRNPC upregulation could indicate adverse outcomes of colorectal cancer patients. In vitro, the knockdown of HNRNPC significantly suppressed the proliferation, migration, and invasion of colorectal cancer cells. CONCLUSIONS: Upregulated HNRNPC served as a biomarker for the prognosis and development of colorectal cancer, which provides a novel therapeutic target for colorectal cancer.
Keywords: N6-methyladenosine (m6A), HNRNPC, colorectal cancer, prognosis, progression
DOI: 10.3233/THC-230429
Journal: Technology and Health Care, vol. 32, no. 3, pp. 1445-1453, 2024
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