Connection of human cytomegalovirus and malignant gliomas of braine
DOI:
https://doi.org/10.25305/unj.61884Keywords:
HCMV, glioblastoma, development by stages interaction tumor, virus, organismAbstract
Elucidation of role HCMV in pathogenesis of glioblastomas is actual task.
Objective: To investigate the presence of HCMV in cells of glioblastomas and to compare with immunologic and hematologic exponents of peripheral blood and size of glioma and its clinical features.
Materials and methods: The presence of HCMV were examined in cells of 53 glioblastomas by means of indirect immunofluorescence with set “HCMV- monoscan” antibodies to protein pp 65 of HCMV (Russia). Proliferative answer was evaluated by means of the reaction blasttransformation on the different mutagens. Hematologic and clinical data were studied in cases reports.
Results: HCMV was examined in 39 (73%) biopsies of glioblastomasfrom studied 53 cases. It was noted more low proliferative activity of T lymphocytes and monocytes/macrophages by using test with indometacyne undoubtedly in patients with HCMV in tumor some more sire of tumor (gate of MRT) in comparison with the patients which HCMV was not determined suggesting the possibility that immune status depends from presence of virus and anaplasia grades O glioma. It discusses some definite successiveness influence of HCMV on immune status contained the alternation of stages the activization and the suppression of immune answer of gliomas different anaplasia grades. It was noted the primary immune suppression in cases of glioblastomas.
Conclusion: The presence HCMV in cells of glioblactomas correlates with suppression of T cells immune answer, this fact does not depends from age, sex, length of disease and peculiarity postoperative course. The size of tumor and more short period of remission correlates with the presence of virus in glioblastomas and rapid growth of tumor. Establishment of main links of the interaction HCMV, tumor and immune system gives the oppoturhute to use this data for the new approaches to antitumor therapy.
References
1. Dziurzynski K, Chang SM, Heimberger AB. Consensus on the role of human cytomegalovirus in glioblastoma. Neuro Oncol. 2012 Mar;14(3):246-55. [CrossRef] [PubMed]
2. Soroceanu L. C.S. Cobbs С.S Is HCMV a tumor promoter? Virus Res. 2011 May;157(2):193-203. [CrossRef] [PubMed]
3. Cobbs ChS. Evading evidence implicates cytomegalovirus as a promoter of malignant glioma pathogenesis. Herpesviridae. 2011 Oct 26;2(1):10. [CrossRef] [PubMed]
4. Scheurer ME, Bondy ML, Aldape KD. Detection of human cytomegalovirus in different histological types of gliomas. Acta Neuropathol. 2008 Jul;116(1):79-86. [CrossRef] [PubMed]
5. Moore PS, Chang Y. Why do viruses cause cancer? Highlights of the first century of human tumour virology. Nat Rev Cancer. 2010 Dec;10(12):878-89. [CrossRef] [PubMed]
6. Cinatl JJr, Vogel JU, Kotchetkov R. Oncomodulatory signals by regulatory proteins encoded by human cytomegalovirus: a novel role for viral infection in tumor progression. Microbiol Rev. 2004:28(1):59-77. [CrossRef] [PubMed]
7. Alibek K, Karpenova A, Baiken Y. Role of infections agents in the carcinogenesis of brain and head and neck cancers. Infect Agent Cancer. 2013 Feb 2;8(1):7. [CrossRef] [PubMed]
8. Poltermann S, Schlehofer B, Steindorf K. Lack of association of herpesviruses with brain tumors. J Neurovirol. 2006 Apr;12(2):90-9. [CrossRef] [PubMed]
9. Lau S, Chen YY, Chen WG. Lack of association of cytomegalovirus with human brain tumors. Mod Pathol. 2005 Jun;18(6):838-43. [CrossRef] [PubMed]
10. Smith W, Tomasec P, Aicheler R, Loewendorf A, Nemčovičovб I, Wang EC, Stanton RJ, Macauley M, Norris P, Willen L, Ruckova E, Nomoto A, Schneider P, Hahn G, Zajonc DM, Ware CF, Wilkinson GW, Benedict CA. Human cytomegalovirus glycoprotein UL14 targets the TRAIL death receptors to thwart host innate antiviral defenses. Cell Host Microbe. 2013 Mar 13;13(3):324-35. [CrossRef] [PubMed]
11. Wei J, Barr J, Kong LY, Glioblastoma cancer-initiating cells inhibit T-cell proliferation and effector responses by the signal transducers and activators of transcription 3 pathway. Mol Cancer Ther. 2010 Jan;9(1):67-78. [CrossRef] [PubMed]
12. Spencer JV, Lockridge KM, Barry PA, Lin G, Tsang M, Penfold ME, Schall TJ. Potent immunosuppressive activities of cytomegalovirus-encoded interleukin-10. J Virol. 2002 Feb;76(3):1285-92. [CrossRef] [PubMed]
13. Luo MH, Schwartz PH, Fortunato EA. Neonatal neural progenitor cells and their neuronal and glial cell derivatives are fully permissive for human cytomegalovirus infection. J Virol. 2008 Oct;82(20):9994-10007. [CrossRef] [PubMed]
14. Odeberg J, Wolmer N, Falci S, Westgren M, Sundtrцm E, Seiger A, Soderberg-Naucler C. Late human cytomegalovirus (HCMV) proteins inhibit differentiation of human neural precursor cells into astrocytes. J Neurosci Res. 2007 Feb 15;85(3):583-93. [CrossRef] [PubMed]
15. Soderberg-Naucler C. HCMV microinfections in inflammatory diseases and cancer. J Clin Virol. 2008 Mar;41(3):218-23. [CrossRef] [PubMed]
16. Rahbar A, Stragliotto G, Orrego A, Peredo I, Taher C, Willems J, Soderberg-Naucler C. Low levels of Human Cytomegalovirus Infection in Glioblastoma multiforme associates with patient survival — a case-control study. Herpesviridae. 2012 Mar 16;3:3. [CrossRef] [PubMed]
17. Kopelian II, Grigor’eva MP. Razrabotka mikro modifikatsii kul’tivirovaniya kletok krovi cheloveka [Development of micromodifications of methods of human blood cell culture]. Biull Eksp Biol Med. 1972 Aug;73(8):119-22. Russian. [PubMed]
18. Dziurzynski K, Wei J, Qiao W, Hatiboglu MA, Kong LY, Wu A, Wang Y, Cahill D, Levine N, Prabhu S, Rao G, Sawaya R, Heimberger AB. Glioma-associated cytomegalovirus mediates subversion of the monocyte lineage to a tumor propagating phenotype. Clin Cancer Res. 2011 Jul 15;17(14):4642-9. [CrossRef] [PubMed]
19. Hadaczek P, Ozawa T, Soroceanu L, Yoshida Y, Matlaf L, Singer E, Fiallos E, James CD, Cobbs CS. Cidofovir: a novel antitumor agent for glioblastoma. Clin Cancer Res. 2013 Dec 1;19(23):6473-83. [CrossRef] [PubMed]
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Copyright (c) 2016 Nikolay Lisianyi, Irina Gnedkova, Diana Stanetskaya, Volodymyr Rozumenko, Mykhaylo Kvasha, Lyudmila Belska, Antonina Klyuchnikova, Anna Shmeleva
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