Serum lncRNAs, NBAT-1, and FOXCUT signature in hepatocellular carcinoma developed on top of chronic hepatitis C

被引:3
作者
Ali, Marwa A. [1 ,9 ]
Shaker, Olfat G. [2 ]
Ezzat, Eman M. [3 ]
Eid, Hanaa M. [4 ]
Ali, Doaa Y. [5 ]
Hassan, Essam A. [6 ]
Elsayed, Dalia H. [7 ]
Abozaid, Eman R. [8 ]
Abdelaleem, Omayma O. [1 ]
机构
[1] Fayoum Univ, Fac Med, Dept Med Biochem & Mol Biol, Al Fayyum, Egypt
[2] Cairo Univ, Fac Med, Dept Med Biochem & Mol Biol, Cairo, Egypt
[3] Fayoum Univ, Fac Med, Dept Internal Med, Al Fayyum, Egypt
[4] Fayoum Univ, Fac Med, Dept Med Microbiol & Immunol, Al Fayyum, Egypt
[5] Fayoum Univ, Fac Med, Dept Clin & Chem Pathol, Al Fayyum, Egypt
[6] Fayoum Univ, Fac Med, Dept Trop Med, Al Fayyum, Egypt
[7] Zagazig Univ, Dept Med Oncol, Zagazig, Egypt
[8] Zagazig Univ, Dept Physiol, Zagazig, Egypt
[9] Fayoum Univ, Fac Med, Dept Med Biochem & Mol Biol, El Gamaa St, Al Fayyum 63514, Egypt
关键词
FOXCUT; HCC; HCV; NBAT-1; LONG NONCODING RNA; EXPRESSION LEVEL; CELL; PROLIFERATION; CANCER; PROGRESSION; ASSOCIATION; METASTASIS; RISK; PAIR;
D O I
10.1002/mc.23488
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundHepatocellular Carcinoma (HCC) is a universal health problem responsible for 8.2% of all cancer deaths. Numerous risk factors were documented to be contributed to HCC development with viral hepatitis C ranking as the major predisposing factor in Egypt. The presence of a detectable amount of long noncoding RNAs (lncRNAs) in the circulation is linked to the development and spread of tumors. LncRNAs NBAT-1 and FOXCUT expression levels were used as genetic markers for the detection of gastrointestinal tract cancers. We hypothesized that serum expression levels of NBAT-1 and FOXCUT are new biomarkers for HCC that are related to laboratory and pathological markers. Patients and MethodsThis study included 165 hepatitis C virus (HCV)-related HCC Egyptian patients, 180 HCV-infected noncancer patients, and 180 healthy controls, the serum expression levels of NBAT-1 and FOXCUT were measured by using quantitative real-time polymerase chain reaction. ResultsThis study's results include that medians (inter-quartile range [IQRs]) of NBAT-1 in HCC and HCV patients were (1.9 [0.87-4.94], 10.01 [7.34-13.29] respectively) which exhibited significantly higher expression than controls, while the medians (IQRs) of FOXCUT in HCC and HCV patients were (0.15 [0.04-0.52], 6.42 [2.49-10.10], respectively) that exhibited significantly lower expression than controls regarding HCC patients but significantly higher expression than controls regarding HCV patients. In comparing serum fold changes of NBAT-1 and FOXCUT between HCC patients and HCV patients; we obtained significantly higher levels of target genes in HCV patients (p < 0.001) than in HCC patients. Also, a positive correlation was detected between NBAT-1 and FOXCUT in HCC group (r = 0.262, p = 0.001) and in HCV group (r = 0.937, p < 0.001). Higher serum NBAT-1 and FOXCUT were significantly associated with better clinical and laboratory data of the disease. Multivariate regression analysis showed that FOXCUT was an independent predictor for HCC among HCV patients (p < 0.001). ConclusionOur study cited that NBAT-1 and FOXCUT could be considered new diagnostic serum biomarkers for HCC on top of HCV.
引用
收藏
页码:319 / 331
页数:13
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