Literature DB >> 22740853

NY-ESO-1 expression in hepatocellular carcinoma: A potential new marker for early recurrence after surgery.

Heng Xu1, Na Gu, Zhao-Bo Liu, Min Zheng, Fang Xiong, Si-Ying Wang, Ning Li, Jun Lu.   

Abstract

NY-ESO-1 belongs to the cancer testis antigens (CTA) family, and is identified in a variety of tumors. Certain studies have demonstrated that NY-ESO-1 predicts tumor recurrence and treatment response. No reports are currently available regarding the correlation between NY-ESO-1 and the recurrence of hepatocellular carcinoma (HCC) following surgery. The purpose of the present study was to evaluate the association between NY-ESO-1 and relapse of HCC and to explore the possible mechanisms for this correlation. A total of 120 HCC patients were analyzed for the expression of NY-ESO-1 by immunohistochemistry (IHC). A stable NY-ESO-1 over-expressed HepG2 cell line (ESO-HepG2) was established to determine the biological effects of NY-ESO-1 on cell proliferation, cell cycle and migration by using the xCELLigence DP system, flow cytometry and xCELLigence SP system. NY-ESO-1 was positive in 28 of 120 (23.3%) HCC tumor tissues. NY-ESO-1 was not detectable in adjacent normal liver tissues. A close correlation was found between NY-ESO-1 expression and the recurrence of HCC following surgery (P=0.007). Kaplan-Meier analysis showed a shorter recurrence-free survival (RFS) for patients positive for NY-ESO-1 (log-rank test, P=0.003). The Cox regression model demonstrated that NY-ESO-1 expression was a significant independent predictor for the recurrence of HCC following curative surgery (P=0.022). Compared with HepG2 cells, ESO-HepG2 cells have increased migration but not proliferation ability. In conclusion, NY-ESO-1 expression is associated with worse HCC outcome following surgery, and the mechanism for this finding may be that NY-ESO-1 increases tumor cell migration.

Entities:  

Year:  2011        PMID: 22740853      PMCID: PMC3362570          DOI: 10.3892/ol.2011.441

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  21 in total

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  13 in total

Review 1.  Current status and perspectives of immune-based therapies for hepatocellular carcinoma.

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Journal:  J Immunother       Date:  2014-04       Impact factor: 4.456

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Journal:  Cancer Immunol Immunother       Date:  2016-02-03       Impact factor: 6.968

Review 5.  The immune system in hepatocellular carcinoma and potential new immunotherapeutic strategies.

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6.  Induction of HCA587-specific antitumor immunity with HCA587 protein formulated with CpG and ISCOM in mice.

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7.  Expression pattern of tumour-associated antigens in hepatocellular carcinoma: association with immune infiltration and disease progression.

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Review 8.  Adaptive immunity in the liver.

Authors:  Zongwen Shuai; Miranda Wy Leung; Xiaosong He; Weici Zhang; Guoxiang Yang; Patrick Sc Leung; M Eric Gershwin
Journal:  Cell Mol Immunol       Date:  2016-03-21       Impact factor: 11.530

9.  Comment on 'Tumour antigen expression in hepatocellular carcinoma in a low-endemic western area'.

Authors:  F Grizzi; D Qehajaj; M Chiriva-Internati; S Stifter
Journal:  Br J Cancer       Date:  2016-04-14       Impact factor: 7.640

10.  Transcriptomic characterization of cancer-testis antigens identifies MAGEA3 as a driver of tumor progression in hepatocellular carcinoma.

Authors:  Amanda J Craig; Teresa Garcia-Lezana; Marina Ruiz de Galarreta; Carlos Villacorta-Martin; Edgar G Kozlova; Sebastiao N Martins-Filho; Johann von Felden; Mehmet Eren Ahsen; Erin Bresnahan; Gabriela Hernandez-Meza; Ismail Labgaa; Delia D'Avola; Myron Schwartz; Josep M Llovet; Daniela Sia; Swan Thung; Bojan Losic; Amaia Lujambio; Augusto Villanueva
Journal:  PLoS Genet       Date:  2021-06-24       Impact factor: 5.917

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