Association of Hepatitis Virus on Acute and Chronic Myeloid Leukemias. A pilot Study
Abstract
Background The induction of cancers incidence by exogenous agents, such as chemical, radiation and especially research on viruses is an interested area of active basic subjects and clinical investigation. Prominent researches sounds a high prevalence of HBV marker has been found in patients with leukemia as compared to the general population.Methods: Present  study was conducted from 1996 to 2010   among patients with chronic acute myeloid leukemia and corresponding with non malignant patients. In this investigation,  Cytochemical staining, immunophenotyping, cytogenetic /molecular cytogenetics, Elisa, enzyme immunoassay and Western blot, were the main subject of laboratory manipulation.Results: Hepatitis B virus was diagnosed in one non malignant control patient (%0.004) and four infected with leukemia patients (%3). The differences of leukemic patients revealed statistical significant when compared with non malignant patients (P=0.0047).Conclusion: In this pilot study, the prevalence of HBV infection was higher in patients with leukemia than in patients as non malignant patients. Our findings are also important as they are among the first to suggest here a potentially significant influence of  HBV infection may plays a probably major role in the process of myeloid malignant development. However, the number of cases are not large enough to draw firm conclusion. Moreover, we suggest that this pilot study, issue warrants further investigation by large consortium project.Blumberg BS, Alter HJ, Visnich S. A "New" Antigen in Leukemia Sera. JAMA. 1965 Feb 15;191:541-6.
Cowan DH, Kouroupis GM, Leers WD. Occurrence of hepatitis and hepatitis B surface antigen in adult patients with acute leukemia. Can Med Assoc J. 1975 Mar 22;112(6):693-7.
Kang J, Cho JH, Suh CW, Lee DH, Oh HB, Sohn YH, et al. High prevalence of hepatitis B and hepatitis C virus infections in Korean patients with hematopoietic malignancies. Ann Hematol. 2011 Feb;90(2):159-64.
Talbot SJ, Crawford DH. Viruses and tumours--an update. Eur J Cancer. 2004 Sep;40(13):1998-2005.
Pontisso P, Vidalino L, Quarta S, Gatta A. Biological and clinical implications of HBV infection in peripheral blood mononuclear cells. Autoimmun Rev. 2008 Oct;8(1):13-7.
Galun E, Ilan Y, Livni N, Ketzinel M, Nahor O, Pizov G, et al. Hepatitis B virus infection associated with hematopoietic tumors. Am J Pathol. 1994 Nov;145(5):1001-7.
Engels EA. Infectious agents as causes of non-Hodgkin lymphoma. Cancer Epidemiol Biomarkers Prev. 2007 Mar;16(3):401-4.
Bautista AP. Neutrophilic infiltration in alcoholic hepatitis. Alcohol. 2002 May;27(1):17-21.
Anderson LA, Pfeiffer R, Warren JL, Landgren O, Gadalla S, Berndt SI, et al. Hematopoietic malignancies associated with viral and alcoholic hepatitis. Cancer Epidemiol Biomarkers Prev. 2008 Nov;17(11):3069-75.
Kiran M, Chawla YK, Kaur J. Methylation profiling of tumor suppressor genes and oncogenes in hepatitis virus-related hepatocellular carcinoma in northern India. Cancer Genet Cytogenet. 2009 Dec;195(2):112-9.
Murakami S. Hepatitis B virus X protein: a multifunctional viral regulator. J Gastroenterol. 2001 Oct;36(10):651-60.
Oishi N, Shilagardi K, Nakamoto Y, Honda M, Kaneko S, Murakami S. Hepatitis B virus X protein overcomes oncogenic RAS-induced senescence in human immortalized cells. Cancer Sci. 2007 Oct;98(10):1540-8.
Brothman AR, Persons DL, Shaffer LG. Nomenclature evolution: Changes in the ISCN from the 2005 to the 2009 edition. Cytogenet Genome Res. 2009;127(1):1-4.
Wands JR, Chura CM, Roll FJ, Maddrey WC. Serial studies of hepatitis-associated antigen and antibody in patients receiving antitumor chemotherapy for myeloproliferative and lymphoproliferative disorders. Gastroenterology. 1975 Jan;68(1):105-12.
Tabor E, Gerety RJ, Mott M, Wilbur J. Prevalence of hepatitis B in a high-risk setting: a serologic study of patients and staff in a pediatric oncology unit. Pediatrics. 1978 May;61(5):711-5.
Romet-Lemonne JL, McLane MF, Elfassi E, Haseltine WA, Azocar J, Essex M. Hepatitis B virus infection in cultured human lymphoblastoid cells. Science. 1983 Aug 12;221(4611):667-9.
Pontisso P, Locasciulli A, Schiavon E, Cattoretti G, Schiro R, Stenico D, et al. Detection of hepatitis B virus DNA sequences in bone marrow of children with leukemia. Cancer. 1987 Jan 15;59(2):292-6.
Evans AS, Mueller NE. Viruses and cancer. Causal associations. Ann Epidemiol. 1990 Oct;1(1):71-92.
Lamelin JP, Trepo C. The hepatitis B virus and the peripheral blood mononuclear cells: a brief review. J Hepatol. 1990 Jan;10(1):120-4.
Matsuo K, Kusano A, Sugumar A, Nakamura S, Tajima K, Mueller NE. Effect of hepatitis C virus infection on the risk of non-Hodgkin's lymphoma: a meta-analysis of epidemiological studies. Cancer Sci. 2004 Sep;95(9):745-52.
Park SC, Jeong SH, Kim J, Han CJ, Kim YC, Choi KS, et al. High prevalence of hepatitis B virus infection in patients with B-cell non-Hodgkin's lymphoma in Korea. J Med Virol. 2008 Jun;80(6):960-6.
Zeldis JB, Mugishima H, Steinberg HN, Nir E, Gale RP. In vitro hepatitis B virus infection of human bone marrow cells. J Clin Invest. 1986 Aug;78(2):411-7.
Sheu JC. Molecular mechanism of hepatocarcinogenesis. J Gastroenterol Hepatol. 1997 Oct;12(9-10):S309-13.
Piotrowski A, Benetkiewicz M, Menzel U, Diaz de Stahl T, Mantripragada K, Grigelionis G, et al. Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer. Genes Chromosomes Cancer. 2006 Jul;45(7):656-67.
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Issue | Vol 3 No 3&4 (2011) | |
Section | Original Articles | |
Keywords | ||
Leukemia AML CML HBV Association |
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