BCL-2 Gene Expression Effect on Haematological Profiles among CML Patients in Ile –Ife. Osun State. Nigeria
DOI:
https://doi.org/10.47743/jemb-2026-253Keywords:
B-Cell Lymphoma 2 gene, chronic myelogenous leukemic, leucocytosis, anaemia, neutrophiliaAbstract
BCL-2 was the first anti-death gene. A key for oncogenic mechanism in several haematological malignancies, has been attributed to the upregulation of BCL-2 which is caused by numerous mechanisms. The aim of the study is to evaluate the BCL-2 gene mutation by its expression level and the resultant effect on haematological profiles among Chronic Myelogenous Leukemic (CML) patients in Ile Ife. This study was cross-sectional and a total of 100 consenting participants were recruited: 50 known CML patients and 50 control subjects. Obafemi Awolowo University Teaching Hospital Complex, Ile-Ife, a Referral Centre for haematologic malignancies, and Seventh Day Adventist Hospital, Ile-Ife, were used as the study centers. Full blood count was done using 3-part haematology auto analyzer (Mindray), while RNA extraction and qPCR Bcl-2 quantification were done using real time PCR equipment. The results obtained from the study shows that there are higher expression levels of the Bcl-2 gene in CML samples compared with control samples, attaining significant p<0.05. Bcl-2 overexpression, suggests that dysregulated Bcl-2 is potentially involved in the pathogenesis of CML. The haematology parameters also shows significant effect of Bcl-2 mutation (p<0.05) as follows: 30% leukocytosis was observed in CML with gene expression compared to normal leukocyte count observed among 43(86%) control and 29(58%) CML with no gene expression. It was noted that more than halve i.e 24% CML with overexpression have anaemia while more than halve i.e.44%CML with no expression and 70%control has normal PCV. The 14% thrombocytosis among the CML with gene expression compared to 2% among the non-expressed CML and 4% among the control is prognostic. The overexpression observed in this study is suggestive of a level that is characteristic of CML patients, and its association with anaemia, leukocytosis and neutrophilia and can be used in the evaluation of the disease and aid in the BCL-2 therapy.
References
Jannah Patty, D. N. ., Ayu Safitri, T. and Saraswati, H. (2020): Specific Primer for Human Bcl-2-Protein Expression Analysis”, KnE Life Sciences, 5(2). doi: 10.18502/kls.v5i2.6438.
Reed John, C. (2008). Bcl-2–family proteins and hematologic malignancies: history and future prospects. Blood. ; 111:3322-3330.
Vaux, D.L., Cory, S., Adams, J.M. (1988). Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells. Nature. 335(6189):440–2.
Cory, S. and Adams, J.M. (2002).The BCL2 family: regulators of the cellular life-or-death switch. Nat Rev Cancer; 2(9):647-656.
Tsujimoto, Y., Gorham, J., Cossman, J., Jaffe, E. and Croce CM. (1985). The t(14;18) chromosome translocations involved in B-cell neoplasms result from mistakes in VDJ joining. Science. 229(4720):1390–1393.
Moia, R., Diop, F., Favini, C., Kodipad, A.A. and Gaidano, G. (2018). Potential of BCL2 as a target for chronic lymphocytic leukemia treatment. Expert Rev Hematol; 11(5):391-402.
Huang, D. C. and Strasser, (2000). A. BH3-only proteins - Gatekeepers of apoptosis. Cell Death and Differentiation, 14(7), 1515-1523.
Huang,Y., Wu, S., Zhu, X., Wu, J. and Zhong, S. (2018). The BCL-2 family contributes to neuronal development and survival by regulating apoptotic and non-apoptotic functions. Cell Death and Differentiation, 2018; 25(1), 127-142.
Roberts, A.W. and Huang, D. (2017). Targeting BCL2 with BH3 mimetics: basic science and clinical application of Venetoclax in chronic lymphocytic leukemia and related B cell malignancies. Clinical Pharmacology Therapeutics. 101(1):89–98.
Fresa, A., Innocenti, I., Tomasso, A., Stirparo, L., Mosca, A., Iadevaia, F., Autore, F., Ghia, P. and Laurenti, L. (2024). Treatment Sequencing in Chronic Lymphocytic Leukemia in 2024: Where We Are and Where We Are Headed. Cancers, 16(11), 2011. https://doi.org/10.3390/cancers16112011
Perini, G. F., Ribeiro, G. N., Pinto Neto, J. V., Campos, L. T. and Hamerschlak, N. (2018). BCL-2 as a therapeutic target for hematological malignancies. Journal of Hematology & Oncology, 11(1), 65. https://doi.org/10.1186/s13045-018-0615-4
Xu, J., Zhai, L., Liu, Y., Zhou, Z. and Li, C. (2022). Bcl-2 family proteins; Guardians of cardiomyocyte survival in physiological and pathological conditions: Frontiers in cell and Development Biology, 10, 820205.
Miettinen, J. J., Pulkki, K., Mustonen, J., Kokko, A. and Elenius, K. (2021). BCL-2 protein expression in acute myeloid leukemia with t(8;21) translocation and its prognostic significance. Leukemia Research, 108, 104595.
Ross, A.M., Leahy, C.I., Neylon, F., Steigerova, J., Flodr, P., Navratilova, M., …Murray, P.G. (2023). Epstein-Barr Virus and the Pathogenesis of Diffusse Large B-Cell Lymphoma. Life, 13(2), 521. https://doi.org/10.3390/life13020521
Zhang, W., Du, F., Wang, L., Bai, T., Zhou, X. and Mei, H. (2023). Hepatitis Virus-associated Non-Hodgkin Lymphoma: Pathogenesis and Treatment Strategies. Journal of Clinical and Translational Hepatology, 11(5), 1256-1266. https://doi.org/10.14218/JCTH.2022.000795
Obazelu, P.A. and Anyafulu, F.C. (2025). Expression of BCL-2 and BAD Genes in Benzene-induced Haematotoxicity Bearing Wistar Rats Treated with Bi-Herbal Formular of Picralima Nitida and Cymbopogon Citratus Extract. African Journal of Laboratory Haematology and Transfusion Science, 4(2), 172-186. Retrieved from htpps://www.ajol.info/index.php/ajlhts/article/view/300333
Liu, Y., Zou, Z., Ou, Q., Sun, L., Liu, J., Sun, Y. and Wang, Y. (2018). FoxO3a controls erythrocyte differentiation and iron metabolism through FBXW7-mediated degradation of Bach1. Nature Communications; 9(1), 1-13.
Ku, C. H., Liu, Y., Cheng, Y. H., Chen, S. W. and Chen, K. Y. (2018). Bcl-2 overexpression extends erythrocyte lifespan but reduces deformability in mice. Blood Cells, Molecules, and Diseases,; 71(1), 74-80.
Yip, K. W., Wong, K. S. and Au, F. T. K. (2020). Bcl-2 family proteins in chronic lymphocytic leukemia: Therapeutic targets. Blood; 136(1), 49-60.
Melo, J.V., Rocha, V., Martins, L.R., Jerónimo, C., Lobo, C., Gärtner, F. and Medeiros, R. (2010). Bcl-2 overexpression in chronic myeloid leukemia: A survival mechanism. Leukemia Research; 34(5): 607-613.
Hu, Y., Liu, Y., Zhuang, L., Xu, Y., Guo, Y., Li, Q. and Zhao, K. (2012). BCR-ABL1 upregulates Bcl-2 expression through JAK2/STAT3 and PI3K/Akt pathways in human chronic myeloid leukemia cells. Biochemical and Biophysical Research Communications, 429(1-2), 120-125.
Wang, C., Li, M., Li, S., Liu, X. and Peng, Y. (2017). The role of Bcl-2 family proteins in chronic myeloid leukemia. Oncotarget, 8(10), 16224-16234.
Sina Ojuade (1992). The issue of “Oduduwa” in Yoruba Genesis: The Myths and Realities,” in TransAfrican Journal of History, Vol. 21, p 143
Huang, D., Wang, X., Li, L., Zhang, Y., Zhang, H., Li, Z. and Li, J. (2019). Bcl-2 deficiency impairs megakaryocyte maturation and platelet production through BIM activation. Cell Death & Differentiation; 26(11), 2576-2590.
Adebola, F.B., Sanusi, A.R. and Adegoke, N.A. (2015). Consequences of road Traffic accident in Nigeria: Time series approach dept of statistics, FUTA Akure. International journal of computer applications Technology and Research; 4:262-273.
Out, T.I. and Ejike, U.G. (2021). The frequency and Pattern of Haematological Malignancies in A Tertiary Hospital in Abuja, Federal Capital Territory, North Central Nigeria: A sixteen Year Review. IOSR journal of Dental and Medical Sciences (IOSR-Jdms); 20(5 Ser.11), 38-44.
Liu, X., Zou, H., Liu, Y. and Zhu, Y. (2019). Regulation of Bcl-2 family proteins in aging. Aging (Albany NY), 11(12), 4005-4022.
Giona, F. and Bianchi, S. (2022). Update in Childhood Chronic Myeloid Leukemia. Hematology, 3(4), 718-730. https://doi.org./10.3390/hemato.3040048
Lee, J. H., Cho, Y. H., Kim, H. J., Kim, S. J., Kim, D. W. and Jang, S. Y. (2021). Gene expression profiling of chronic myeloid leukemia patients and healthy controls. Genes & Genomics, 43(10), 707-715.
Czeten, M. and Fulda, S. (2020). BCL-2 family wrestling: crosstalk at the crossroads of life and death. Cell Death & Differentiation, 27(10), 2609-2622.
Zhang, W., Hu, X., Chen, S., Sun, Y. and Liu, Z. (2023). BCL-2 family proteins and drug resistance in leukemia. Journal of Experimental & Clinical Cancer Research, 42(1), 7.
Downloads
Published
How to Cite
License
Copyright (c) 2026 Samson Elujoba

This work is licensed under a Creative Commons Attribution 4.0 International License.
This journal provides immediate open access to its content on the principle that making research freely available to the public supports a greater global exchange of knowledge. The journal allows readers to read, download, copy, distribute, print, search, link to the full texts or use the articles for any other lawful purpose.
The authors are the sole copyright owners of the published articles. The articles are distributed under the CC BY 4.0 license to the readers.
The readers are free to:
Share — copy and redistribute the material in any medium or format
Adapt — remix, transform, and build upon the material for any purpose, even commercially
Under the following terms:
Attribution — You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
No additional restrictions — you may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.






