Distinction immune genes of hepatitis-induced heptatocellular carcinoma

Hu, Jinyu and Gao, Zhiwei (2012) Distinction immune genes of hepatitis-induced heptatocellular carcinoma. Bioinformatics, 28 (24). pp. 3191-3194. ISSN 1367-4803

WarningThere is a more recent version of this item available.
Full text not available from this repository.
Official URL: http://dx.doi.org/10.1093/bioinformatics/bts624

Abstract

Motivation: Hepatitis B virus and hepatitis C virus are the two leading causes resulting in hepatocellular carcinoma (HCC). It is observed that hepatitis C virus (HCV) is relatively difficult to induce HCC compared with hepatitis B virus (HBV). This motivates us to reveal the reasons behind this from the viewpoint of immune genes.

Results: In order to distinguish the immune genes with low-level expression in HBV-induced HCC, but high-level expression in HCV-induced HCC, the concept of distinction immune gene is proposed. A filter is then designed to screen these genes. By using gene positive network with strong correlations between genes, the genes are further filtered to form the set of key distinction immune genes. The twenty-three key distinction immune genes are screened, which are divided into four clusters: T cells, B cells, immune signaling, and MHC. It is evident that the screened genes are important immune genes, which are activated in HCV-induced HCC, but inactivated in HBV-induced HCC. In HCV-induced HCC, the structures of HCV adaptively update so that they are difficult to be identified by antigens. Therefore, the clinic advice is either to increase the update speed of antigens or reduce the update speed of the viruses during the treatment of HCV-induced HCC. Moreover, it is also advised to add T cells or add the expression levels of T cells to strengthen the ability to kill cancer cells. In contrast, HBV updates slowly, but the immunity system in HBV-induced HCC has been damaged seriously. As a result, the clinic advice is to improve the immune ability of patients subjected to HBV-induced HCC, such as increasing immunoglobulin, T cells, and B cells etc.

Item Type: Article
Subjects: H100 General Engineering
Department: ?? 7920 ??
Depositing User: Dr Zhiwei Gao
Date Deposited: 10 Dec 2012 09:36
Last Modified: 13 Oct 2019 00:44
URI: http://nrl.northumbria.ac.uk/id/eprint/10541

Available Versions of this Item

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics