Human S15a expression is upregulated by hepatitis B virus X protein

Lian Z., Liu J., Li L., Li X., Tufan N. L., Wu M., ...Daha Fazla

MOLECULAR CARCINOGENESIS, sa.1, ss.34-46, 2004 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1002/mc.20012
  • Dergi Adı: MOLECULAR CARCINOGENESIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.34-46
  • Anahtar Kelimeler: hepatocarcinogenesis, hepatitis B x antigen, rhosomal protein, translation, GROWTH-FACTOR-BETA, PROMOTES HEPATOCELLULAR GROWTH, RIBOSOMAL-PROTEIN, PROTEASOME COMPLEX, TRANSLATION INITIATION, MOLECULAR-CLONING, GENE PRODUCT(S), CELLULAR GENE, LIVER-CANCER, HBX PROTEIN
  • Ankara Üniversitesi Adresli: Hayır

Özet

The hepatitis B virus (HBV)-encoded 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 HBxAg-positive and -negative HepG2 cells were compared by PCR select cDNA subtraction. One gene overexpressed in HBxAg-positive 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 HBV-infected 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. (C) 2004 Wiley-Liss, Inc.