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      Normal and prostate cancer cells display distinct molecular profiles of alpha-tubulin posttranslational modifications.

      The Prostate
      Acetylation, Androgens, physiology, Blotting, Western, Cell Line, Cell Line, Tumor, Disease Progression, Electrophoresis, Polyacrylamide Gel, Epithelium, chemistry, metabolism, pathology, Humans, Male, Microscopy, Fluorescence, Peptide Synthases, analysis, Polyglutamic Acid, Prostate, cytology, Prostatic Neoplasms, Protein Processing, Post-Translational, Receptors, Androgen, Tubulin, Tyrosine

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          Abstract

          Multiple diverse posttranslational modifications of alpha-tubulin such as detyrosination, further cleavage of the penultimate glutamate residue (Delta2-tubulin), acetylation, and polyglutamylation increase the structural and functional diversity of microtubules. Herein, we characterized the molecular profile of alpha-tubulin posttranslational modifications in normal human prostate epithelial cells (PrEC), immortalized normal prostate epithelial cells (PZ-HPV-7), androgen-dependent prostate cancer cells (LNCaP), transitional androgen-independent prostate cancer cells (LNCaP-cds and CWR22Rv1), and androgen-independent prostate cancer cells (PC3). Compared to PrEC and PZ-HPV-7 cells, all cancer cells exhibited elevated levels of detyrosinated and polyglutamylated alpha-tubulin, that was paralleled by decreased protein levels of tubulin tyrosine ligase (TTL). In contrast, PrEC and PZ-HPV-7 cells expressed markedly higher levels of Delta2-tubulin. Whereas alpha-tubulin acetylation levels were generally equivalent in all the cell lines, PC3 cells did not display detectable levels of Ac-tubulin. These data may reveal novel biomarkers of prostate cancer and new therapeutic targets. Copyright 2006 Wiley-Liss, Inc.

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