𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Oncogenic human papillomaviruses block expression of the B-cell translocation gene-2 tumor suppressor gene

✍ Scribed by Claire Cullmann; Karin Hoppe-Seyler; Susanne Dymalla; Claudia Lohrey; Martin Scheffner; Matthias Dürst; Felix Hoppe-Seyler


Publisher
John Wiley and Sons
Year
2009
Tongue
French
Weight
283 KB
Volume
125
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Human papillomavirus (HPV)‐induced carcinogenesis is critically dependent on the activities of the viral E6 and E7 oncogenes. Here, we demonstrate that expression of the putative tumor suppressor gene B‐cell translocation gene‐2 (BTG2) is reinduced in HPV16‐ and HPV18‐positive cancer cells on silencing of viral oncogene expression, indicating that BTG2 is repressed by oncogenic HPVs. Inhibition of BTG2 expression was mediated by the HPV E6 oncogene and occurred in a p53‐dependent manner. Luciferase reporter gene analyses revealed that BTG2 repression takes place at the transcriptional level and is dependent on the integrity of the major p53‐response element within the BTG2 promoter. Ectopic expression of BTG2 acted antiproliferative in cervical cancer cells. Tissue specimens commonly exhibited reduced BTG2 protein levels in HPV‐positive high‐grade lesions (CIN2/3) and cervical carcinomas, when compared with normal cervical epithelium. These findings identify the antiproliferative BTG2 gene as a novel cellular target blocked by the HPV E6 oncoprotein. © 2009 UICC


📜 SIMILAR VOLUMES


Expression of oncogenes and tumor suppre
✍ Mahmood Farshid; Dr. Edward Tabor 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 592 KB

## Abstract The expression of nine oncogenes (c‐myc, N‐myc, N‐ras, H‐ras, k‐ras, abl, fos, src, and raf) and two tumor suppressor genes (p53 and RB) were studied by northern blot hybridization in six human hepatocellular carcinoma or hepatoblastoma cell lines (PLC/PRF/5, HepSB, Hep G2, 2.2.15, HLE,

The expression of the tumor suppressor g
✍ Jadranka Loncarek; Hiroshi Yamasaki; Pierre Levillain; Serge Milinkevitch; Marc 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 439 KB

## Abstract Gap junctional intercellular communication is thought to play an important role in cell differentiation and tissue homeostasis. Gap junctional intercellular communication is mediated by intercellular channels connecting adjacent cells and composed of connexin (Cx) proteins. Until now, a

Codeletion of the JUN proto-oncogene and
✍ Jian-Nian Zhou; Sofia Ljungdahl; Dan Röhme; Göran Levan; Maria C. Shoshan; Stig 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 181 KB 👁 2 views

The cyclin kinase inhibitor p16, encoded by the CDKN2A gene, suppresses the transformation of mouse embryonic fibroblasts by oncogenic RAS. In contrast, the c-JUN transcription factor (a major component of AP-1) has been suggested to be required for RAS transformation of rodent fibroblasts. The CDKN

Selective induction of cell cycle regula
✍ Jinsong You; R. Curtis Bird 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 962 KB

Genes encoding cdkl (~34'~''), cyclin A, cyclin B, and the tumor suppressor gene Rb are fundamental regulators of cell cycle progression which associate as a complex with the transcription factor E2F. Expression of many of these proteins has previously been shown to be repressed by okadaic acid, a s