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Article type: Research Article
Authors: Srivastava, Meera | Bubendorf, Lukas; | Nolan, Lisa | Glasman, Mirta | Leighton, Ximena | Miller, Georgina | Fehrle, Wilfred | Raffeld, Mark | Eidelman, Ofer | Kallioniemi, Olli P. | Srivastava, Shiv | Pollard, Harvey B.
Affiliations: Department of Anatomy, Physiology and Genetics, and Institute for Molecular Medicine, Uniformed Services University School of Medicine (USUHS), Bethesda, MD 20814, USA | Section on Molecular Genetics, Cancer Genetics Branch, NHGRI, National Institutes of Health, Bethesda, MD 20892, USA | Veterinary Resources Program, NCRR, National Institutes of Health, Bethesda, MD 20892, USA | Laboratory of Pathology, Hematopathology section, NCI, NIH, Bethesda, MD 20892, USA | Institute for Pathology, University of Basel, Switzerland | Center for Prostate Disease Research, and Department of Surgery, Uniformed Services University School of Medicine (USUHS), Bethesda, MD 20814, USA
Note: [] Department of Anatomy and Cell Biology, USU School of Medicine, 4301 Jones Bridge Road, Bethesda, MD 20814, USA. Tel.: +1 301 295 3204; Fax: +1 301 295 2822; E-mail: msrivastava@usuhs.mil
Abstract: The ANX7 gene codes for a Ca^{2+}-activated GTPase, which has been implicated in both exocytotic secretion in cells and control of growth. In this review, we summarize information regarding increased tumor frequency in the Anx7 knockout mice, ANX7 growth suppression of human cancer cell lines, and ANX7 expression in human tumor tissue micro-arrays. The loss of ANX7 is significant in metastatic and hormone refractory prostate cancer compared to benign prostatic hyperplasia. In addition, ANX7 expression has prognostic value for predicting survival of breast cancer patients.
Journal: Disease Markers, vol. 17, no. 2, pp. 115-120, 2001
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