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Downregulated Expression of Chromobox Homolog 7 in Hepatocellular Carcinoma.
- Source :
-
Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2019 May; Vol. 23 (5), pp. 348-352. Date of Electronic Publication: 2019 Apr 16. - Publication Year :
- 2019
-
Abstract
- Background: As an essential member of the Polycomb group (PcG) proteins, chromobox homolog 7 (CBX7) is found deregulated in some human cancers, and is thought to be a contributing factor in carcinogenesis. However, the expression and role of CBX7 in hepatocellular carcinoma (HCC) is still not well characterized. Materials and Methods: The levels of the CBX7 protein were quantified in 75 paired HCC and adjacent nontumor tissues by immunohistochemistry; comparisons were made using McNemar's chi-square test. The Kaplan-Meier estimate was used for survival analysis. Results: We found that the expression of CBX7 in HCC tissues was significantly lower than that of adjacent nontumor tissues. In addition, decreased CBX7 expression levels were correlated with liver cirrhosis in HCC patients. Furthermore, the survival times of HCC patients who were CBX7-expression-negative were shorter than HCC patients who were CBX7-expression-positive. Conclusion: Our results show that downregulation of CBX7 is related to HCC progression and a poor prognosis in HCC patients.
- Subjects :
- Adult
Aged
Asian People genetics
Carcinoma, Hepatocellular metabolism
Cell Line, Tumor
China
Disease Progression
Down-Regulation
Female
Gene Frequency
Genetic Predisposition to Disease
Genotype
Humans
Kaplan-Meier Estimate
Liver Neoplasms metabolism
Male
Middle Aged
Polymorphism, Single Nucleotide genetics
Prognosis
Carcinoma, Hepatocellular genetics
Liver Neoplasms genetics
Polycomb Repressive Complex 1 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1945-0257
- Volume :
- 23
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Genetic testing and molecular biomarkers
- Publication Type :
- Academic Journal
- Accession number :
- 30990338
- Full Text :
- https://doi.org/10.1089/gtmb.2018.0293