Glyceraldehyde-3-phosphate dehydrogenase expression during apoptosis and proliferation of rat ventral prostate

Biology of Reproduction

Volumn 61, Issue 3, 1999, Pages 687-691

  Epner, Daniel E ^a   Sawa, Akira ^b   Isaacs, John T ^c  

^a MICHAEL E DEBAKEY VETERANS AFFAIRS MEDICAL CENTER   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CASTRATION; CELL PROLIFERATION; CELLULAR DISTRIBUTION; CONTROLLED STUDY; EPITHELIUM CELL; IMMUNOHISTOCHEMISTRY; MALE; NONHUMAN; PRIORITY JOURNAL; PROSTATE VENTRAL LOBE; PROTEIN EXPRESSION; RAT;

ANIMALS; APOPTOSIS; CELL DIVISION; CELL NUCLEUS; CYTOPLASM; EPITHELIAL CELLS; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASES; IMMUNOHISTOCHEMISTRY; MALE; ORCHIECTOMY; PROSTATE; RATS; RATS, SPRAGUE-DAWLEY; TESTOSTERONE;

ANIMALIA;

EID: 0032779337     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod61.3.687     Document Type: Article

References (26)

1. Epner DE, Coffey DS. There are multiple forms of glyceraldehyde-3-phosphate dehydrogenase in prostate cancer cells and normal prostate tissue. Prostate 1996; 28:372-378.
2. Sunaga K, Takahashi H, Chuang DM, Ishitani R. Glyceraldehyde-3-phosphate dehydrogenase is over-expressed during apoptotic death of neuronal cultures and is recognized by a monoclonal antibody against amyloid plaques from Alzheimer's brain. Neurosci Lett 1995; 200: 133-136.
3. Ishitani R, Sunaga K, Tanaka M, Aishita H, Chuang DM. Overexpression of glyceraldehyde-3-phosphate dehydrogenase is involved in low K+-induced apoptosis but not necrosis of cultured cerebellar granule cells. Mol Pharmacol 1997; 51:542-550.
4. Ishitani R, Kimura M, Sunaga K, Katsube N, Tanaka M, Chuang DM. An antisense oligodeoxynucleotide to glyceraldehyde-3-phosphate dehydrogenase blocks age-induced apoptosis of mature cerebrocortical neurons in culture. J Pharmacol Exp Ther 1996; 278:447-454.
5. Sawa A, Khan AA, Hester LD, Snyder SH. Glyceraldehyde-3-phosphate dehydrogenase: nuclear translocation participates in neuronal and nonneuronal cell death. Proc Natl Acad Sci USA 1997; 94: 11669-11674.
6. Ishitani R, Sunaga K, Hirano A, Saunders P, Katsube N, Chuang DM. Evidence that glyceraldehyde-3-phosphate dehydrogenase is involved in age-induced apoptosis in mature cerebellar neurons in culture. J Neurochem 1996; 66:928-935.
7. Ishitani R, Chuang DM. Glyceraldehyde-3-phosphate dehydrogenase antisense oligodeoxynucleotides protect against cytosine arabinonucleoside-induced apoptosis in cultured cerebellar neurons. Proc Natl Acad Sci USA 1996; 93:9937-9941.
8. English HF, Santen RJ, Isaacs JT. Response of glandular versus basal rat ventral prostatic epithelial cells to androgen withdrawal and replacement. Prostate 1987; 11:229-242.
9. Banerjee PP, Banerjee S, Tilly KI, Tilly JL, Brown TR, Zirkin BR. Lobe-specific apoptotic cell death in rat prostate after androgen ablation by castration. Endocrinology 1995; 136:4368-4376.
10. Colombel MC, Buttyan R. Hormonal control of apoptosis: the rat prostate gland as a model system. Methods Cell Biol 1995; 46:369-385.
11. Evans GS, Chandler JA. Cell proliferation studies in the rat prostate: II. The effects of castration and androgen-induced regeneration upon basal and secretory cell proliferation. Prostate 1987; 11:339-351.
12. Kerr JF, Searle J. Deletion of cells by apoptosis during castrationinduced involution of the rat prostate. Virchows Arch B Cell Pathol 1973; 13:87-102.
13. Culic O, Gruwel ML, Schrader J. Energy turnover of vascular endothelial cells. Am J Physiol 1997; 273:C205-C213.
14. Berges RR, Furuya Y, Remington L, English HF, Jacks T, Isaacs JT. Cell proliferation, DNA repair, and p53 function are not required for programmed death of prostatic glandular cells induced by androgen ablation. Proc Natl Acad Sci USA 1993; 90:8910-8914.
15. r 32,000 nuclear phosphoprotein is selectively expressed in cells competent for self-renewal. Cancer Res 1993; 53:4720-4726.
16. deKlerk DP, Heston WD, Coffey DS. Studies on the role of macromolecular synthesis in the growth of the prostate. In: Grayhack JT, Wilson JE, Scherbenske MJ (eds.), Benign Prostatic Hyperplasia: A Workshop Sponsored by the Kidney Disease and Urology Program of the National Institute of Arthritis, Metabolism, and Digestive Diseases. Bethesda, MD: Department of Health, Education, and Welfare publication no. (NIH) 76-1113.
17. Sirover MA. Role of the glycolytic protein, glyceraldehyde-3-phosphate dehydrogenase, in normal cell function and in cell pathology. J Cell Biochem 1997; 66:133-140.
18. Sirover MA. Minireview. Emerging new functions of the glycolytic protein, glyceraldehyde-3-phosphate dehydrogenase, in mammalian cells. Life Sci 1996; 58:2271-2277.
19. Meyer-Siegler K, Mauro DJ, Seal G, Wurzer J, DeRiel JK, Sirover MA. A human nuclear uracil DNA glycosylase is the 37-kDa subunit of glyceraldehyde-3-phosphate dehydrogenase. Proc Natl Acad Sci USA 1991; 88:8460-8464.
20. Polgar PR, Foster JM, Cooperband SR. Glycolysis as an energy source for stimulation of lymphocytes by phytohemagglutinin. Exp Cell Res 1968; 49:231-237.
21. Burger C, Wick M, Brusselbach S, Muller R. Differential induction of "metabolic genes" after mitogen stimulation and during normal cell cycle progression. J Cell Sci 1994; 107:241-252.
22. Sariban-Sohraby S, Magrath IT, Balaban RS. Comparison of energy metabolism in human normal and neoplastic (Burkitt's lymphoma) lymphoid cells. Cancer Res 1983; 43:4662-4664.
23. Marjanovic S, Skog S, Heiden T, Tribukait B, Nelson BD. Expression of glycolytic isoenzymes in activated human peripheral lymphocytes: cell cycle analysis using flow cytometry. Exp Cell Res 1991; 193:425-431.
24. Greiner EF, Guppy M, Brand K. Glucose is essential for proliferation and the glycolytic enzyme induction that provokes a transition to glycolytic energy production. J Biol Chem 1994; 269:31484-31490.
25. Wada HG, Indelicato SR, Meyer L, Kitamura T, Miyajima A, Kirk G, Muir VC, Parce JW. GM-CSF triggers a rapid, glucose dependent extracellular acidification by TF-1 cells: evidence for sodium/proton antiporter and PKC mediated activation of acid production. J Cell Physiol 1993; 154:129-138.
26. Epner DE, Partin AW, Schalken JA, Isaacs JT, Coffey DS. Association of glyceraldehyde-3-phosphate dehydrogenase expression with cell motility and metastatic potential of rat prostatic adenocarcinoma. Cancer Res 1993; 53:1995-1997.