SPARC Overexpression Promotes Liver Cancer Cell Proliferation and Tumor Growth
Autor: | Lan Yang, Xia-nan Wu, Hui-Zhong Zhang, Ke Dong, Ting He, Zhao-wei Gao, Chong Liu |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Sorafenib
Cell growth QH301-705.5 proliferation SPARC bioinformatics Biology medicine.disease Biochemistry Genetics and Molecular Biology (miscellaneous) Biochemistry Peripheral blood mononuclear cell Extracellular matrix liver cancer tumor growth Hepatocellular carcinoma Cancer cell medicine Cancer research Immunohistochemistry Molecular Biosciences Biology (General) Liver cancer Molecular Biology medicine.drug Original Research |
Zdroj: | Frontiers in Molecular Biosciences Frontiers in Molecular Biosciences, Vol 8 (2021) |
ISSN: | 2296-889X |
Popis: | Background:Secreted protein acidic and rich in cysteine (SPARC) plays an important role in cancer development. The roles of SPARC in the liver hepatocellular carcinoma (LIHC) are unclear.Methods:GEPIA2 and UALCAN were used to analyze the SPARC mRNA expression levels in LIHC based on the TCGA database. The GEO database was used to verify the analysis results. Immunohistochemical (IHC) analysis was used to investigate the SPARC protein levels in LIHC tissues. The Kaplan–Meier (KM) plotter was used to analyze the correlation between SPARC and prognosis. The serum SPARC levels were measured by ELISA. CCK8 and murine xenograft models were used to investigate the effect of SPARC on the liver cancer growthin vitroandin vivo. SPARC-correlated genes were screened by LinkedOmics.Results:Based on the TCGA and GEO databases, the analysis showed that the SPARC mRNA expression levels were increased in tumor tissues and peripheral blood mononuclear cell (PBMC) from LIHC compared to normal controls. The IHC analysis showed an increased level of SPARC in LIHC tissues compared to adjacent non-tumor tissues. However, we found that the serum SPARC levels were lower in LIHC than those in healthy controls. The KM plotter showed that there was no significant correlation between the SPARC mRNA levels and overall survival. However, in sorafenib-treated LIHC patients, the high SPARC expression predicts favorable prognosis. Furthermore, the endogenous SPARC overexpression promotes liver cancer cell proliferationin vitroand tumor growthin vivo, while there was no significant effect of exogenous SPARC treatment on liver cancer cell proliferation. Function enrichment analysis of SPARC-correlated genes indicated a critical role of interaction with an extracellular matrix in SPARC-promoting cancer cell proliferation.Conclusion:SPARC mRNAs were increased in LIHC tumor tissues, and SPARC overexpression may promote the liver cancer growth. Further studies are needed to clarify the potential prognostic value of SPARC, both in tissues and in circulation. |
Databáze: | OpenAIRE |
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