## Abstract Spent tissue culture medium (CDM‐S) removed from a single cell line of human malignant melanoma grown in serum‐free CDM, contained tumor‐associated antigenic activity. Antibodies to CDM‐S measured by complement fixation were detected in 44% (31/70) melanoma, 55% (15/27) sarcoma, 63% (24
Detection of human polyomavirus proteins, T-antigen and agnoprotein, in human tumor tissue arrays
✍ Scribed by Luis Del Valle; Kamel Khalili
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 387 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Expression of the human polyomavirus JCV genome in several experimental animals induces a variety of neural origin tumors. The viral proteins, T‐antigen and Agnoprotein, contribute to the oncogenesis of JCV by associating with several tumor suppressor proteins and dysregulating signaling pathways, which results in uncontrolled cell proliferation. In addition, T‐antigen and Agnoprotein have been associated with DNA damage and interfering with DNA repair mechanisms. In this study, we have utilized commercially available tissue arrays of human tumors of various origins and demonstrated the expression of both T‐antigen and Agnoprotein in some, but not all, tumors of neural and non‐neural origin. Most notably, more than 40% of human glioblastomas and greater than 30% of colon adenocarcinomas express viral proteins. The detection of viral transforming proteins, T‐antigen and Agnoprotein in the absence of viral capsid proteins suggests a role for JCV in the development and/or progression of human tumors. These results invite further large‐scale investigation on the role of polyomaviruses, particularly JCV in the pathogenesis of human cancer. J. Med. Virol. 82: 806–811, 2010. © 2010 Wiley‐Liss, Inc.
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