Upregulation of mortalin/mthsp70/Grp75 contributes to human carcinogenesis.

Abstract

Mortalin, also known as mthsp70/GRP75/PBP74, interacts with the tumor suppressor protein p53 and inactivates its transcriptional activation and apoptotic functions. Here, we examined the level of mortalin expression in a large variety of tumor tissues, tumor-derived and in vitro immortalized human cells. It was elevated in many human tumors, and in all of the tumor-derived and in vitro immortalized cells. In human embryonic fibroblasts immortalized with an expression plasmid for hTERT, the telomerase catalytic subunit, with or without human papillomavirus E6 and E7 genes, we found that subclones with spontaneously increased mortalin expression levels became anchorage-independent and acquired the ability to form tumors in nude mice. Furthermore, overexpression of mortalin was sufficient to increase the malignancy of breast carcinoma cells. The study demonstrates that upregulation of mortalin contributes significantly to tumorigenesis, and thus is a good candidate target for cancer therapy.

• Authors: Renu Wadhwa, Syuichi Takano, Kamaljit Kaur, Custer C Deocaris, Olivia M Pereira-Smith, Roger R Reddel, Sunil C Kaul
• Journal: International journal of cancer (Int J Cancer) Vol. 118 Issue 12 Pg. 2973-80 (Jun 15 2006) ISSN: 0020-7136 [Print] United States
• PMID: 16425258 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2006 Wiley-Liss, Inc.

Chemical References

• DNA-Binding Proteins
• HSP70 Heat-Shock Proteins
• Tumor Suppressor Protein p53
• mortalin
• Telomerase

Topics

• Animals
• Apoptosis
• Blotting, Northern
• Blotting, Western
• Breast Neoplasms (metabolism, pathology)
• Cell Line, Tumor
• Cell Transformation, Neoplastic (metabolism, pathology)
• Chemotaxis
• DNA Fingerprinting
• DNA-Binding Proteins (metabolism)
• Female
• Gene Expression Regulation, Neoplastic
• HSP70 Heat-Shock Proteins (biosynthesis, metabolism)
• Human papillomavirus 6
• Humans
• Mice
• Mice, Inbred BALB C
• Mice, Nude
• Neoplasms (metabolism, pathology)
• Telomerase (metabolism)
• Transcription, Genetic
• Tumor Suppressor Protein p53 (metabolism)
• Up-Regulation