Bovine papillomavirus type-2 DNA and expression of E5 and E7 oncoproteins in vascular tumours of the urinary bladder in cattle

Cancer Letters

Volumn 250, Issue 1, 2007, Pages 82-91

  Borzacchiello, Giuseppe ^a   Russo, Valeria ^a   Spoleto, Claudia ^a   Roperto, Sante ^a   Balcos, Liviu ^c   Rizzo, Consuelo ^b   Venuti, Aldo ^b   Roperto, Franco ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b REGINA ELENA NATIONAL CANCER INSTITUTE   (Italy)

^c UNIVERSITY OF AGRICULTURAL SCIENCES AND VETERINARY MEDICINE   (Romania)

Author keywords

Bovine papillomavirus type 2; Bracken fern; E5; E7; Mesenchymal tumours

Indexed keywords

DNA; PLATELET DERIVED GROWTH FACTOR BETA RECEPTOR; PROTEIN E5; PROTEIN E7; UNCLASSIFIED DRUG; VIRUS PROTEIN;

ANIMAL TISSUE; ARTICLE; BLADDER TUMOR; BLOOD VESSEL; CATTLE; CONTROLLED STUDY; ENDOTHELIUM CELL; IMMUNOFLUORESCENCE; NONHUMAN; PAPILLOMA VIRUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; TUMOR CELL; VASCULAR TUMOR;

ANIMALS; BOVINE PAPILLOMAVIRUS 1; CATTLE; CATTLE DISEASES; DNA, VIRAL; ONCOGENE PROTEINS; ONCOGENE PROTEINS, VIRAL; RECEPTOR, PLATELET-DERIVED GROWTH FACTOR BETA; URINARY BLADDER NEOPLASMS; VASCULAR NEOPLASMS;

BOS; BOVINE PAPILLOMAVIRUS TYPE 2; PTERIDIUM AQUILINUM;

EID: 33947604804     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2006.09.022     Document Type: Article

References (40)

1. Pamukcu A.M., Price J.M., and Bryan G.T. Naturally occurring and bracken fern-induced bovine urinary bladder tumors. Clinical and morphological characteristics. Vet. Pathol. 13 (1976) 110-122
2. Pamukcu A.M. Tumours of the urinary bladder. Bull. World Health Organ. 50 (1974) 43-52
3. Smith B.L. The toxicity of bracken fern (genus Pteridium) to animals and its relevance to man. In: Felix D'Mello J.P. (Ed). Handbook of Plant and Fungal Toxicants (1997), CRC Press, Boca Raton, FL, USA
4. Borzacchiello G., Ambrosio V., Galati P., Perillo A., and Roperto F. Cyclooxygenase-1 and -2 expression in urothelial carcinomas of the urinary bladder in cows. Vet. Pathol. 40 (2003) 455-459
5. Campo M.S., Jarrett W.F., Barron R., O'Neil B.W., and Smith K.T. Association of bovine papillomavirus type 2 and bracken fern with bladder cancer in cattle. Cancer Res. 52 (1992) 6898-6904
6. IARC Monographs on the Evaluation of Carcinogenic Risks to Human (1995), vol. 64, Human Papillomavirus. IARC, Lyon, France.
7. Sundberg J.P. Papillomavirus infections in animals. In: Syrjanen K., Gissmann L., and Koss L. (Eds). Papillomaviruses and Human Disease (1987), Springer-Verlag, Heidelberg, Germany 40-103
8. Sundberg J.P., VanRanst M., Burk R.D., and Jenson A.B. The nonhuman (animal) papillomaviruses: host range, epitope conservation, and molecular diversity. In: Gross G., and vonKrogh G. (Eds). Human Papillomavirus Infections in Dermatology and Venereology (1996), CRC Press, Boca Raton, FL, USA 47-68
9. de Villiers E.M., Fauquet C., Broker T.R., Bernard H.U., and zur Hausen H. Classification of papillomaviruses. Virology 324 (2004) 17-27
10. Borzacchiello G., Iovane G., Marcante M.L., Poggiali F., Roperto F., Roperto S., and Venuti A. Presence of bovine papillomavirus type 2 DNA and expression of the viral oncoprotein E5 in naturally occurring urinary bladder tumours in cows. J. Gen. Virol. 84 (2003) 2921-2926
11. Schiller J.T., Vass W.C., Vousdn K.H., and Lowy D.R. E5 open reading frame of bovine papillomavirus type 1 encodes a transforming gene. J. Virol. 57 (1986) 1-6
12. Schlegel R., Wade-Glass M., Rabson M.S., and Yang Y.C. The E5 transforming gene of bovine papillomavirus encodes a small, hydrophobic polypeptide. Science 233 (1986) 464-467
13. Burnett S., Jareborg N., and DiMaio D. Localization of bovine papillomavirus type 1 E5 protein to transformed basal keratinocytes and permissive differentiated cells in fibropapilloma tissue. Proc. Natl. Acad. Sci. USA 89 (1992) 5665-5669
14. Anderson R.A., Scobie L., O'Neil B.W., Grindlay G.J., and Campo M.S. Viral proteins of bovine papillomavirus type 4 during the development of alimentary canal tumours. Vet. J. 154 (1997) 69-78
15. Venuti A., and Campo M.S. The E5 protein of papillomavirus. In: McCance D. (Ed). Human Papillomavirus - Perspectives in Medical Virology vol. 8 (2002), Elsevier Science B.V., Amsterdam 143-164
16. Burkhardt A., Willingham M., Gay C., Jeang K.T., and Schlegel R. The E5 oncoprotein of bovine papillomavirus is oriented asymmetrically in Golgi and plasma membranes. Virology 170 (1989) 334-339
17. Pennie W.D., Grindlay G.J., Cairney M., and Campo M.S. Analysis of the transforming functions of bovine papillomavirus type 4. Virology 193 (1993) 614-620
18. Araibi E.H., Marchetti B., Ashrafi G.H., and Campo M.S. Downregulation of major histocompatibility complex class I in bovine papillomas. J. Gen. Virol. 85 (2004) 2809-2814
19. Bohl J., Hull B., and Vande Pol S.B. Cooperative transformation and coexpression of bovine papillomavirus type 1 E5 and E7 proteins. J. Virol. 75 (2001) 513-521
20. Finbow M.E., Pitts J.D., Goldstein D.J., Schlegel R., and Findlay J.B. The E5 oncoprotein target: a 16-kDa channel-forming protein with diverse functions. Mol. Carcinog. 4 (1991) 441-444
21. Goldstein D.J., Finbow M.E., Andresson T., McLean P., Smith K., Bubb V., and Schlegel R. Bovine papillomavirus E5 oncoprotein binds to the 16K component of vacuolar H(+)-ATPases. Nature 352 (1991) 347-349
22. Conrad M., Bubb V.J., and Schlegel R. The human papillomavirus type 6 and 16 E5 proteins are membrane-associated proteins which associate with the 16-kilodalton pore-forming protein. J. Virol. 67 (1993) 6170-6178
23. Faccini A.M., Cairney M., Ashrafi G.H., Finbow M.E., Campo M.S., and Pitts J.D. The bovine papillomavirus type 4 E8 protein binds to ductin and causes loss of gap junctional intercellular communication in primary fibroblasts. J. Virol. 70 (1996) 9041-9045
24. Ashrafi G.H., Tsirimonaki E., Marchetti B., O'Brien P.M., Sibbet G.J., Andrew L., and Campo M.S. Down-regulation of MHC class I by bovine papillomavirus E5 oncoproteins. Oncogene 10 21 2 (2002) 248-259
25. Marchetti B., Ashrafi G., Tsirimonaki E., O'Brien P.M., and Campo M.S. The bovine papillomavirus oncoprotein E5 retains MHC class I molecules in the Golgi apparatus and prevents their transport to the cell surface. Oncogene 21 (2002) 7808-7816
26. Petti L., Nilson L.A., and DiMaio D. Activation of the platelet-derived growth factor receptor by the bovine papillomavirus E5 transforming protein. EMBO J. 10 (1991) 845-855
27. DiMaio D., and Mattoon D. Mechanisms of cell transformation by papillomavirus E5 proteins. Oncogene 20 (2001) 7866-7873
28. DeMasi J., Huh K.W., Nakatani Y., Munger K., and Howley P.M. Bovine papillomavirus E7 transformation function correlates with cellular p600 protein binding. Proc. Natl. Acad. Sci. USA 102 (2005) 11486-11491
29. Huh K.W., DeMasi J., Ogawa H., Nakatani Y., Howley P.M., and Munger K. Association of the human papillomavirus type 16 E7 oncoprotein with the 600-kDa retinoblastoma protein-associated factor, p600. Proc. Natl. Acad. Sci. USA 102 (2005) 11492-11497
30. Borzacchiello G., Russo V., Gentile F., Roperto F., Venuti A., Nitsch L., Campo M.S., and Roperto S. Bovine papillomavirus E5 oncoprotein binds to the activated form of the platelet-derived growth factor β receptor in naturally occurring bovine urinary bladder tumours. Oncogene 25 (2006) 1251-1260
31. Carvalho T., Pinto C., and Peleteiro M. Urinary bladder lesions in bovine enzootic haematuria. J. Comp. Pathol. 134 (2006) 336-346
32. Borzacchiello G., Ambrosio V., Galati P., Poggiali F., Venuti A., and Roperto F. The pagetoid variant of urothelial carcinoma in situ of urinary bladder in a cow. Vet. Pathol. 38 (2001) 113-116
33. Colitti M., Wilde C.J., and Stefanon B. Functional expression of bcl-2 protein family and AIF in bovine mammary tissue in early lactation. J. Dairy Res. 71 (2004) 20-27
34. Jarrett W.F.H. The natural history of bovine papillomavirus infection. In: Klein G. (Ed). Advances in Viral Oncology vol. 5 (1985), Raven Press, NewYork 83-101
35. Jelinek F., and Tachezy R. Cutaneous papillomatosis in cattle. J. Comp. Pathol. 132 (2005) 70-81
36. Campo M.S., Jarrett W.F., O'Neil V., and Barron R.J. Latent papillomavirus infection in cattle. Res. Vet. Sci. 56 (1994) 151-157
37. Chambers G., Ellsmore V.A., O'Brien P.M., Reid S.W.J., Love S., Campo M.S., and Nasir L. Association of bovine papillomavirus with the equine sarcoid. J. Gen. Virol. 84 (2003) 1055-1062
38. Alles J., and Bosslet K. Immunocytochemistry of angiosarcomas: a study of 19 cases with special emphasis on the applicability of endothelial cell specific markers to routinely prepared tissue. Am. J. Clin. Pathol. 89 (1988) 463-471
39. Füle T., Màthè M., Suba S., Csapò Z., Szarva T., Tàtrai P., Paku S., and Kovalszky I. The presence of human papillomavirus 16 in neural structures and vascular endothelial cells. Virology 348 (2006) 289-296
40. Leptak C., Ramon y Cajal S., Kulke R., Horwitz B.H., Riese D.J., Dotto G.P., and DiMaio D. Tumorigenic transformation of mouse keratinocytes by the E5 genes of human papillomavirus type 16 and bovine papillomavirus type 1. J. Virol. 65 (1991) 7078-7083