Expression of heme oxygenase-1 (HSP32) in human prostate: Normal, hyperplastic, and tumor tissue distribution

Urology

Volumn 47, Issue 5, 1996, Pages 727-733

  Maines, Mahin D ^a   Abrahamsson, Per Anders ^b  

^a UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BILIVERDIN; CARBON MONOXIDE; HEAT SHOCK PROTEIN; HEME; HEME OXYGENASE; IRON; ISOENZYME; MESSENGER RNA; PROTOPORPHYRIN;

ADULT; AGED; ANIMAL TISSUE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ASSAY; GENE EXPRESSION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MICROSOME; NONHUMAN; NORTHERN BLOTTING; PRIORITY JOURNAL; PROSTATE CARCINOMA; PROSTATE HYPERTROPHY; PROSTATE TUMOR; PROSTATECTOMY; RAT; TISSUE DISTRIBUTION;

EID: 0030003896     PISSN: 00904295     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0090-4295(96)00010-6     Document Type: Article

References (48)

1. Pelham HRB: Speculations on the functions of the major heat shock and glucose-regulated proteins. Cell 46: 959-961, 1986.
2. Lindquist S, and Craig EA: The heat shock proteins. Annu Rev Genet 22: 631-677, 1988.
3. Morimoto RI, Abravaya K, Mosser D, and Williams GT: Transcription of the human HSP70 gene: cis-acting elements and trans-acting factors involved in basal, adenovirus E1A, and stress-induced expression, in Schlesinger M, Santoro M, Garaci M (Eds): Stress Proteins, Berlin, Springer-Verlag, 1990, pp 1-17.
4. Lindquist S: Autoregulation of heat-shock response, in Ilan J (Ed): Translational Regulation of Gene Expression 2. New York, Plenum Publishers, 1993, pp 279-319.
5. Zakeri ZF, and Wolgemuth DJ: Developmental-stage-specific expression of the HSP 70 gene family during differentiation of the mammalian germ line. Mol Cell Biol 7: 1791-1796, 1987.
6. Aaeri AF, Wolgemuth DJ, and Hunt CR: Identification and sequence analysis of a new member of the mouse HSP70 gene family and characterization of its unique cellular and development pattern of expression in the male germ line. Mol Cell Biol 8: 2925-2932, 1988.
7. Gruppi CM, Zakeri ZF, and Wolgemuth DJ: Stage and lineage regulated expression of two HSP90 transcripts during mouse germ cell differentiation and embryogenesis. Mol Reprod Dev 28: 209-217, 1991.
8. Pinto M, Morange M, and Bensaude O: Denaturation of proteins during heat shock. In vivo recovery of solubility and activity of reporter enzymes. J Biol Chem 266: 13941-13946, 1991.
9. Maines MD, Trakshel GM, and Kutty RK: Characterization of two constitutive forms of rat liver microsomal heme oxygenase: only one molecular species of the enzyme is inducible. J Biol Chem 261: 411-419, 1986.
10. Cruse I, and Maines MD: Evidence suggesting that the two forms of heme oxygenase are products of different genes. J Biol Chem 263: 3348-3353, 1988,
11. Smith MA, Kutty RK, Richey PL, Yan SD, Stern D, Chader GJ, Wiggert B, Petersen RB, and Perry G: Heme oxygenase-1 is associated with the neurofibrillary pathology of Alzheimer's disease. Am J Pathol 145: 42-47, 1994.
12. Mukhtar N, Lee IP, Foureman GL, and Bend JR: Epoxide metabolizing enzyme activities in rat testes: postnatal development and relative activity in interstitial and spermatogenic cell compartments. Chem Biol Interact 22: 153-165, 1978.
13. Hääparanta T, Glaumann H, and Gustafsson J: Characterization and endocrine regulation of the cytochrome P450 dependent microsomal hydroxylation of 5α-androstane-3β, 17β-diol in the rat ventral prostate. Endocrinology 114: 2293-2300, 1984.
14. Soderkvist P, Poellinger L, Toftgard R, and Gustafsson JA: Differential expression of the cytochrome P-450c and p-450d genes in the rat ventral prostate and liver. Cancer Res 48: 3045-3049, 1988.
15. Iscan M, and Maines MD: Differential regulation of heme and drug metabolism in rat testis and prostate: response to cis-platinum and human chorionic gonadotropin. J Pharmacol Exp Ther 253: 73-79, 1990.
16. Maines MD: Effect of cis-platinum on heme, drug and steroid metabolism pathways: possible involvement in infertility and nephrotoxicity. CRC Crit Rev Toxicol 21: 1-20, 1990.
17. Gemzik B, and Parkinson A: Hydroxylation of 5α-androstane-3β, 17β-diol by rat prostate microsomes: potent inhibition by imidazole-type antimycotic drugs and lack of inhibition by steroid 5α-reductase inhibitors. Arch Biochem Biophys 296: 366-373, 1992.
18. Trakshel GM, Kutty RK, and Maines MD: Purification and characterization of the major constitutive form of testicular heme oxygenase: The non-inducible isoform. J Biol Chem 261: 11131-11137, 1986.
19. Maines MD: Heme Oxygenase: Clinical Applications and Functions. Boca Raton, CRC Press, 1992, pp 1-276.
20. Maines MD, Chung A-S, and Kutty RK: Inhibition of testicular heme oxygenase activity by cadmium: a novel cellular response. J Biol Chem 257: 14116-14121, 1982,
21. Maines MD, and Jollie DR: Dissociation of heme metabolic activities from the microsomal cyt P-450 turnover in teslis of hypophysectomized rats. J Biol Chem 259: 9557-9562, 1984.
22. Stocker R, Yamamato Y, McDonagh AF, Glaser AN, and Ames BN: Bilirubin is an antioxidant of possible physiological importance. Science 235: 1043-1046, 1987.
23. Maines MD: Carbon monoxide: an emerging regulator of cGMP in the brain. Mol Cell Neurosci 4: 389-397, 1993.
24. Maines MD, Mark J, and Ewing J: Heme oxygenase, a likely regulator of cGMP production in the brain: induction in vivo of HO-1 compensates for depression in NO synthase activity. Mol Cell Neurosci 4: 398-397, 1993.
25. Ewing RJ, Raju VS, and Maines MD: Induction of heart heme oxygenase-1 (HSP32) by hyperthermia: possible role in stress-mediated elevation of cyclic 3′:5′-guanosine monophosphate. J Pharmacol Exp Ther 271: 408-414, 1994.
26. Prabhakar NR, Dinerman JL, Agani FH, and Snyder SH: Carbon monoxide: a role in carotid body chemoreception. Proc Natl Acad Sci USA 92: 1994-1997, 1995.
27. Maines MD, and Kappas A: Metals as regulators of heme metabolism: physiological and toxicological implications. Science 198: 1215-1221, 1977.
28. Harford JB, Casey JL, Koeller DM, and Klausner RD: Structure, function and regulation of the transferrin receptor: insights from molecular biology, in Steer CJ, and Hanover JA (Eds): Intracellular Trafficking of Proteins. Cambridge, Cambridge University Press, 1991, pp 302-334.
29. Vile GF, and Tyrell RM: Oxidative stress resulting from UVA irradiation of human skin fibroblasts leads to a heme oxygenase-dependent increase in ferritin. J Biol Chem 268: 14678-14681, 1993.
30. Weiss G, Werner-Felmayer G, Werner ER, Grünewald K, Wachter H, and Hentze MW: Iron regulates nitric oxide synthase activity by controlling nuclear transcription. J Exp Med 180: 969-976, 1994.
31. Rossi MC, and Zetter BR: Selective stimulation of prostatic carcinoma cell proliferation by transferrin. Proc Natl Acad Sci USA 89: 6197-6201, 1992.
32. Pollak M: Reversal by transferrin of growth-inhibitory effect of suramin on hormone-refractory human prostate cancer cells (letter). J Natl Cancer Inst 87: 608-609, 1995.
33. Sato Y, Mukai K, Watanabe S, Goto M, and Shimosato Y: The AmEX method. A simplified technique of tissue processing and paraffin embedding with improved preservation of antigens for immunostaining. Am J Pathol 125: 431-435, 1986.
34. Lowry OH, Rosebrough NJ, Farr AL, and Randall RJ: Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265-275, 1951.
35. Rotenberg MO, and Maines MD: Isolation, characterization, and expression in Escherichia coli of a cDNA encoding rat heme oxygenase-2. J Biol Chem 265: 7501-7506, 1990.
36. Shibahara S, Müller R, Taguchi H, and Yoshida T: Cloning and expression of cDNA for rat heme oxygenase. Biochem 82: 7865-7869, 1985.
37. Chirgwin JM, Przbyla AE, MacDonald RJ, and Rutter WJ: Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18: 5294-5299, 1979.
38. Sun Y, Rotenberg MO, and Maines MD: Developmental expression of heme oxygenase isozymes in rat brain: two HO-2 mRNAs are detected. J Biol Chem 265: 8212-8217, 1990.
39. Ewing JF, and Maines MD: In situ hybridization and immunohistochemical localization of heme oxygenase-2 mRNA and protein in normal rat brain: differential distribution of isozyme 1 and 2. J Neurochem 60: 1512-1519, 1993.
40. Kato S, Morita T, Takenaka T, Kato M, Hirano A, Herz F, and Ohama E: Stress-response (heat-shock) protein 90 expression in tumors of the central nervous system: an immunohistochemical study. Acta Neuropathol 89: 184-188, 1995.
41. Storm FK, Gilchrist KW, Warner TF, and Mahvi DM: Distribution of Hsp-27 and HER-2/neu in in situ and invasive ductal breast carcinomas. Ann Surg Oncol 2: 43-48, 1995.
42. Love S, and King RJ: A 27 kDa heat shock protein that has anomalous prognostic powers in early and advanced breast cancer. Br J Cancer 69: 743-748, 1994.
43. Elledge RM, Clark GM, Fuqua SA, Yu YY, and Allred DC: p53 protein accumulation detected by five different antibodies: relationship to prognosis and heat shock protein 70 in breast cancer. Cancer Res 54: 3752-3752, 1994.
44. Takahashi S, Mikami T, Watanabe Y, Okazaki M, Okazaki Y, Okazaki A, Sato T, Asaishi K, Hirata K, Narimatsu E, et al: Correlation of heat shock protein 70 expression with estrogen receptor levels in invasive human breast cancer. Am J Clin Pathol 101: 519-525, 1994.
45. Ponka P, Borova J, Neuwirt J, Fuchs O, and Necas E: A study of intracellular iron metabolism using pyridoxal isonicotinoyl hydrazone and other synthetic chelating agents. Biochim Biophys Acta 586: 278-282, 1979.
46. Landschultz W, Thesleff I, and Ekblom P: A lipophilic iron chelator can replace transferrin as a stimulator of cell proliferation and differentiation. J Cell Biol 98: 596-601, 1984.
47. Kühn LC, Schulman HM, and Ponka P: Iron-transferrin requirements and transferrin receptor expression in proliferating cells, in Ponka P, Schulman HM, and Woodworth RC (Eds): Iron Transport and Storage. Boca Raton, CRC Press, 1990, pp 149-191.
48. Huggenvik T, Sylvester SR, and Griswold MD: Control of transferrin mRNA synthesis in Sertoli cells. Ann NY Acad Sci 438: 1-7, 1984.