Long Noncoding RNAs MALAT1 and HOTTIP Act as Serum Biomarkers for Hepatocellular Carcinoma

• Published in: Cancer control 2024-01, Vol.31, p.10732748241284821
• Main Authors: Bao, Han, Jiang, Yutian, Wang, Ning, Su, Hongying, Han, Xiangjun
• Format: Article
• Language: English
• Subjects: Adult; alpha-Fetoproteins - analysis; alpha-Fetoproteins - metabolism; Biomarkers, Tumor - blood; Biomarkers, Tumor - genetics; Carcinoma, Hepatocellular - blood; Carcinoma, Hepatocellular - diagnosis; Carcinoma, Hepatocellular - genetics; Case-Control Studies; Female; Gene Expression Regulation, Neoplastic; Humans; Liver Neoplasms - blood; Liver Neoplasms - diagnosis; Liver Neoplasms - genetics; Male; Middle Aged; Prognosis; Prospective Studies; RNA, Long Noncoding - blood; RNA, Long Noncoding - genetics; ROC Curve
• ISSN: 1073-2748; 1526-2359; 1526-2359
• DOI: 10.1177/10732748241284821

Circulating tumor markers with satisfactory sensitivity and specificity play crucial roles in cancer diagnosis and therapy. This prospective study aimed to evaluate the potential of circulating lncRNAs as biomarkers for hepatocellular carcinoma (HCC). A total of 74 patients with HCC and 94 healthy controls were enrolled. The expression levels of candidate genes in serum were detected by qRT-PCR. Receiver operating characteristic (ROC) curve analysis and logistic regression were employed to investigate the diagnostic capacity of lncRNAs. The analysis of 3-year overall survival (OS) was conducted using the Kaplan-Meier method and log-rank test. Of the 9 candidate genes, 6 lncRNAs could be stably detected in serum. The expression levels of circulating MALAT1 and HOTTIP in HCC patients were significantly higher than those in controls ( < 0.001). ROC analysis showed that MALAT1 and HOTTIP were more effective than alpha-fetoprotein (AFP) ( < 0.010) in the diagnosis of HCC, with AUCs of 0.896 and 0.899, respectively. Additionally, a panel consisting of MALAT1, HOTTIP, and AFP was constructed to obtain an AUC of 0.968 with a sensitivity of 87.8% and specificity of 94.7% in HCC diagnosis. Moreover, the upregulation of MALAT1 was not only related to multiple tumor lesions, HCV infection, AST level, and AFP level, but also suggested shorter OS. A high expression level of HOTTIP was associated with metastasis. Serum MALAT1 and HOTTIP play indicative roles as non-invasive biomarkers for HCC.