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Clinicopathological Significance and Expression Pattern of Bcl2 in Breast Cancer: A Comprehensive in silico and in vitro Study.
Sofi, Shazia; Mehraj, Umar; Jan, Nusrat; Almilaibary, Abdullah; Ahmad, Irshad; Ahmad, Fuzail; Ahmad Mir, Manzoor.
Afiliación
  • Sofi S; Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar 190006, India.
  • Mehraj U; Department of pathology, Duke University, Durham, NC 27708, United States.
  • Jan N; Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar 190006, India.
  • Almilaibary A; Department of Family & Community Medicine, Faculty of Medicine, Al Baha University, Albaha 65511, Saudi Arabia.
  • Ahmad I; Department of Medical Rehabilitation Sciences, CAMS, King Khalid University, Abha, Saudi Arabia.
  • Ahmad F; College of Applied Sciences, Almaarefa University, Diriya, Riyadh 13713, Saudi Arabia.
  • Ahmad Mir M; Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar 190006, India.
Saudi J Biol Sci ; 31(2): 103916, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38223131
ABSTRACT
B-cell lymphoma/leukemia gene-2 (Bcl-2) is the primary proto-oncogene that has been shown to work by preventing apoptosis/programmed cell death. Bcl-2 combines a variety of cell-generated signals associated to the survival and death of cells. In glioma, lung, and breast cancer, Bcl-2 over-expression has been linked to an increase in invasion and migration. Many treatment regimens that target Bcl2 have been established and approved, and thus increasing the survival rates of the patients. The primary goal of this research was to recognize new therapeutic compounds that target Bcl2 and assess Bcl2 expression pattern in BC patients. We used various bioinformatic tools as well as several in vitro assays to look out the expression and inhibition of Bcl2 in BC. Our study depicted that Bcl2 had a strong connection with tumour stroma, notably with suppressor cells originating from myeloid tissues. Moreover, in vitro and in silico research identified Paclitaxel as a promising natural substance that targets Bcl2. Overall, this work shows that Bcl2 overexpression accelerates the development of BC, and that targeting Bcl2 in combination with other drugs will dramatically improve BC patient's response to treatment and prevent the emergence of drug resistance.
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