## Abstract The hepatitis B virus X protein (HBx) plays an important role in the development of hepatocellular carcinoma (HCC). The relationship was examined between HBV antigens and IAP (inhibitor of apoptosis) family in development of HCC. The expression levels of HBV antigens (HBsAg, HBcAg, and
Human S15a expression is upregulated by hepatitis B virus X protein
โ Scribed by Zhaorui Lian; Jie Liu; Li Li; Xianxing Li; N. Lale Satiroglu Tufan; Meng-Chao Wu; Hong-Yang Wang; Patrick Arbuthnot; Michael Kew; Mark A. Feitelson
- Book ID
- 102944069
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 682 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0899-1987
- DOI
- 10.1002/mc.20012
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โฆ Synopsis
Abstract
The hepatitis B virus (HBV)โencoded X antigen (HBxAg) may contribute to the development of hepatocellular carcinoma (HCC) through the upregulated expression of selected cellular genes. To identify these genes, RNAs isolated from HBxAgโpositive and โnegative HepG2 cells were compared by PCR select cDNA subtraction. One gene overexpressed in HBxAgโpositive cells by Northern and Western blotting is the ribosomal protein S15a. The S15a mRNA is 535 base pairs, encoding a protein 130 amino acids long with a molecular weight of 14.3 kDa. S15a expression was upregulated in HBVโinfected livers, where it costained with HBxAg. Overexpression of S15a stimulated cell growth, colony formation in soft agar, and tumor formation in SCID mice. Hence, HBxAg upregulated the expression of S15a, the latter of which participates in the development of HCC, perhaps by altering the integrity of translation. ยฉ 2004 WileyโLiss, Inc.
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## Abstract The hepatitis B virus (HBV) is a major cause of human hepatocellular carcinoma (HCC) which has a very high mortality rate due to high incidence of metastasis. It is unknown whether HBV contributes to HCC metastasis. In this report, we present clinical data obtained from HCC patients ind
The X protein can act on the enhancer of hepatitis B virus in an in uitro system and elevate the transcriptional level of hepatitis B virus. However, because no relationship had been reported between X protein expression and hepatitis B virus replication in patients with chronic hepatitis B, we focu