Abstract

BackgroundThis study determined the regulatory effects of inducible T-cell co-stimulators (ICOS) in human hepatocellular carcinoma HepG2 cells using a RNA interference (RNAi) technique.MethodsA RNAi technique was used to knockdown the expression of ICOS. ICOS expression after knockdown was detected as mRNA and protein levels by RT-PCR and Western blot, respectively. A MTT colorimetric assay was used to detect cell proliferation, and the Transwell assay was used to detect cell invasion. Western blot was carried out to detect the level of Bcl-2, AKT, and PI3K protein expression in different groups.ResultsThe proliferation of HepG2 cells were significantly decreased after ICOS siRNA transfection (EG group). Similarly, the results of the Transwell experiment showed that invasion of HepG2 cells in the EG group was clearly reduced compared to the negative control (NC) and blank control groups (CON). Western blot analysis showed that knockdown of ICOS expression reduced the levels of Bcl-2 and AKT, and also significantly up-regulated the level of PI3K phosphorylation (P < 0.01).ConclusionDown-regulating ICOS expression in HepG2 cells suppressed cell proliferation and invasion. The underlying mechanism may be related to the expression of the downstream factor, PI3K/AKT.

Highlights

  • This study determined the regulatory effects of inducible T-cell co-stimulators (ICOS) in human hepatocellular carcinoma HepG2 cells using a RNA interference (RNAi) technique

  • The present study provides the experimental and theoretical bases for exploring the effect of the ICOS gene in liver cancer and provide a new scientific perspective to illustrate the pathogenesis of liver cancer

  • According to the data issued by the World Health Organization (WHO), the global incidence of primary hepatocellular carcinoma (HCC) is RNA interference is a gene silencing technology which can induce base sequence homology mRNA degradation with the use of double-stranded RNA to reduce the expression of the targeted gene

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Summary

Introduction

This study determined the regulatory effects of inducible T-cell co-stimulators (ICOS) in human hepatocellular carcinoma HepG2 cells using a RNA interference (RNAi) technique. Primary hepatocellular carcinoma (HCC) is a malignant tumor with a high incidence and mortality rate in China. The incidence of HCC ranks 4th among malignant tumors in China [1, 2]. In 1999, scientists found a new co-stimulatory molecule in the human immune system [inducible co-stimulators (ICOS)]. Recent studies have shown that ICOS may have certain functions involving the proliferation and invasion of tumors [7, 8]. Tumor cells can escape from immune system surveillance via several mechanisms, and further grow, divide, and proliferate. Recent studies have shown that T cell-mediated immunity is a major anti-tumor immune mechanism in humans, and the activation

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