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Expression of inducible nitric oxide synthase in human breast cancer depends on tumor grade

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Abstract

Expression of inducible nitric oxide synthase (iNOS) by tumor cells has been suggested to abrogate metastasis in several tumor models, whereas constitutive NOS expression correlated positively with tumor grade in human breast carcinoma. Whether or not expression of one of the various NOS isoforms could predict the prognosis of breast cancer, however, has not been established. In the present report we investigated the cellular distribution of NOS isoforms in a series of benign and malignant breast tumors and in normal breast tissue. Immunohistochemistry revealed that in samples of benign disease the number of iNOS + epithelial cells or total epithelial cells was 69 ± 16% (n=50). In samples of grade II invasive ductal breast carcinomas the number of iNOS+ tumor cells or total tumor cells was 62 ± 20 (n=40), compared to 12 ± 9 (n=40) in samples of grade III carcinomas (P < 0.0001). iNOS protein was also identifiable in most of the epithelial cells of normal breast tissue (n=4). In contrast, eNOS protein was restricted to vascular endothelial cells in all of the specimens studied. Since the presence of tumor cell iNOS protein is inversely related to the tumor’s metastatic potential, we conclude that endogenous tumor cell mediated iNOS expression might have an inhibitory effect on the metastatic process in breast cancer.

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References

  1. Moncada S, Palmer RMJ, Higgs EA: Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol Rev 43: 109–142, 1991

    Google Scholar 

  2. Knowles RG, Moncada S: Nitric oxide synthase in mammals. Biochem J 298: 249–258, 1994

    Google Scholar 

  3. Robbins RA, Barnes PJ, Springall DR, Warren JB, Kwon OJ, Buttery LD, Wilson AJ, Gellner DA, Polak JM: Expression of inducible nitric oxide synthase in human lung epithelial cells. Biochem Biophys Res Comm 203: 209–218, 1994

    Google Scholar 

  4. Bloom HJG, Richardson WW: Histologic grading and prognosis in breast cancer. A study of 1409 cases of which 359 have been followed for 15 years. Br J Cancer 11: 359–377, 1957

    Google Scholar 

  5. Thomsen LL, Miles DW, Happerfield L, Bobrow LG, Knowles RG, Moncada S: Nitric oxide synthase activity in human breast cancer. Br J Cancer 72: 41–44, 1995

    Google Scholar 

  6. Tschugguel W, Knogler W, Czerwenka K, Mildner M, Weninger W, Zeillinger R, Huber JC: Presence of endothelial calcium-dependent nitric oxide synthase in breast apocrine metaplasia. Br J Cancer 74: 1423–1426, 1996

    Google Scholar 

  7. Konturek SJ, Brzozowski T, Majka J, Pyto-Polonczyk J, Stachura J: Inhibition of nitric oxide synthase delays healing of chronic gastric ulcers. Eur J Pharmacol 239: 215–217, 1993

    Google Scholar 

  8. Macchiarini P, Fontanini G, Hardin MJ, Squartini F, Angeletti CA: Relation of neovascularisation to metastasis of non-small cell lung cancer. Lancet 340: 145–146, 1992

    Google Scholar 

  9. Brawer MK, Deering RE, Brown M, Preston SD, Bigler SA: Predictors of pathologic stage in prostatic carcinoma. The role of neovascularity. Cancer 73: 678–687, 1994

    Google Scholar 

  10. Jenkins DC, Charles IG. Thomsen LL, Moss DW, Holmes LS, Baylis SA, Rhodes P, Westmore K, Emson PC, Moncada S: Roles of nitric oxide in tumour growth. Proc Natl Acad Sci USA 92: 4392–4396, 1995

    Google Scholar 

  11. Xie K, Huang S, Dong Z, Juang SH, Gutman M, Xie Q, Nathan C, Fiedler IJ: Transfection with the inducible nitric oxide synthase gene suppresses tumorigenicity and abrogates metastasis by K-1735 murine melanoma cells. J ExpMed 181: 1333–1343, 1995

    Google Scholar 

  12. Xie K, Huang S, Dong Z, Gutman M, Fidler IJ: Direct correlation between expression of endogenous inducible nitric oxide synthase and regression of M5076 reticulum cell sarcoma hepatic metastases in mice treated with liposomes containing lipopeptide CGP 31362. Cancer Res 55: 3123–3131, 1995

    Google Scholar 

  13. Thomsen LL, Scott JMJ, Topley P, Knowles RG, Keerie AJ, Frend AJ: Selective inhibition of inducible nitric oxide synthase inhibits tumor growth in vivo: studies with 1400W, a novel inhibitor. Cancer Res 57: 3300–3304, 1997

    Google Scholar 

  14. Hermanek P, Scheibe O, Spiessl B, Wagner G: UICC International Union Against Cancer: TNM Klassifikation maligner Tumoren. Springer-Verlag, Berlin, Heidelberg, New York, London, Paris, Tokyo, 1987, pp 100–106

    Google Scholar 

  15. Tschugguel W, Schneeberger C, Unfried G, Czerwenka K, Weninger W, Mildner M, Bishop JR, Huber JC: Induction of inducible nitric oxide synthase expression in human secretory endometrium. Hum Reprod 13: 436–444, 1998

    Google Scholar 

  16. Godfroid B, Geuskens M, Dupressoir T, Parent I, Szpirer C: Cytokeratins are exposed to the outer surface of established human mammary carcinoma cells. J Cell Sci 99: 595–607, 1991

    Google Scholar 

  17. Hembrough TA, Vasudevan J, Allietta MM, Glass WF2nd, Gonias SL: A cytokeratin 8-like protein with plasminogenbinding activity is present on the external surface of hepatocytes, HepG2 cells and breast carcinoma cell lines. J Cell Sci 108: 1071–1082, 1995

    Google Scholar 

  18. Horak ER, Leek R, Klenk N, Lejeune S, Smith K, Stuart N, Greenall M, Stepniewska K, Harris AL: Angiogenesis, assessed by platelet/endothelial cell adhesion molecule antibodies, as indicator of node metastasis and survival in breast cancer. Lancet 340: 1120–1124, 1992

    Google Scholar 

  19. Zeillinger R, Tantscher E, Schneeberger C, Tschugguel W, Eder S, Sliutz G, Huber JC: Simultaneous expression of nitric oxide synthase and estrogen receptor in human breast cancer cell lines. Breast Cancer Res Treat 40: 205–207, 1996

    Google Scholar 

  20. Stuehr DJ, Nathan CF: Nitric oxide: a macrophage product responsible for cytostasis and respiratory inhibition in tumor target cells. J Exp Med 169: 1543–1555, 1989

    Google Scholar 

  21. Cui S, Reichner JS, Mateo RB, Albina JE: Activated murine macrophages induce apoptosis in tumor cells through nitric oxide-dependent or-independent mechanisms. Cancer Res 54: 2462–2467, 1994

    Google Scholar 

  22. Farais-Eisner R, Sherman MP, Aeberhard E, Chaudhuri G: Nitric oxide is an important mediator for tumoricidal activity in vivo. Proc Natl Acad Sci USA 91: 9407–9411, 1994

    Google Scholar 

  23. Thomsen LL, Lawton FG, Knowles RG, Beesley JE, RiverosMoreno V, Moncada S: Nitric oxide synthase activity in human gynecological cancer. Cancer Res 54: 1352–1354, 1994

    Google Scholar 

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Tschugguel, W., Schneeberger, C., Unfried, G. et al. Expression of inducible nitric oxide synthase in human breast cancer depends on tumor grade. Breast Cancer Res Treat 56, 143–149 (1999). https://doi.org/10.1023/A:1006288526311

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