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Alterations in tumor angiogenesis associated with stable expression of the HIV tat gene
Author(s) -
Huber Brian E.,
Richards Cynthia A.,
Martin J. Louise,
Wirth Peter J.
Publication year - 1992
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.2940050410
Subject(s) - biology , microbiology and biotechnology , chloramphenicol acetyltransferase , gene , gene expression , cell culture , transfection , activator (genetics) , fusion gene , plasmid , reporter gene , genetics
Abstract Recent evidence suggests that the human immunodeficiency virus type 1 (HIV) trans ‐activator gene ( tat ) has transforming properties and may be a causative factor in the development of certain types of cancers, in particular Kaposi's sarcoma (i.e., Vogel J. et al. Nature 335:606–611, 1988). To help elucidate the potential role or roles of the HIV tat gene in neoplastic transformation, cell lines were constructed that constitutively express a functional tat gene product. HeLa cells were coelectroporated with two plasmids, one containing the HIV tat gene in an expression cassette and another containing the dominant selectable marker gene xanthine guanine phosphoribosyltransferase (XGPRT). After XGPRT selection, single‐cell clones that expressed a functional tat protein were identified by measuring chloramphenicol acetyltransferase (CAT) activity after electroporating a plasmid containing the CAT gene transcriptionally controlled by HIV trans ‐activation‐responsive region ( tar ). Phenotypic alterations resulting from the expression of tat were then determined. Control cells and tat ‐expressing cells grew at similar rates in culture. However, when grown as tumors in nude mice, tat ‐expressing cells produced a lower percentage of tumors, and the tumors that were produced either regressed, stopped growing, or grew at a very reduced rate compared with cells not expressing tat. These differences may have resulted from a tat ‐associated reduction in neovascularization in the tumors. A comparison of total cellular proteins by two‐dimensional polyacrylamide gel electrophoresis indicated only one reproducible alteration in a polypeptide of approximately 44 kDa and p1 of approximately 6.2 associated with tat expression. These cells may be very useful in future in vitro and in vivo studies designed to examine the effects of HIV tat on endothelial and vascular smooth‐muscle cells and the role of tat in the etiology of Kaposi's sarcoma. © 1992 Wiley‐Liss, Inc.