Anti-Tumor Effect of Cicer Arietinum against the Triple-Negative Breast Cancer Cells
Hassan, H., Sayed, A. (2019). Anti-Tumor Effect of Cicer Arietinum against the Triple-Negative Breast Cancer Cells. EKB Journal Management System, 11(2), 31-41. doi: 10.21608/eajbsz.2019.36226
Hebatallah Hassan; Amany Ahmed Sayed. "Anti-Tumor Effect of Cicer Arietinum against the Triple-Negative Breast Cancer Cells". EKB Journal Management System, 11, 2, 2019, 31-41. doi: 10.21608/eajbsz.2019.36226
Hassan, H., Sayed, A. (2019). 'Anti-Tumor Effect of Cicer Arietinum against the Triple-Negative Breast Cancer Cells', EKB Journal Management System, 11(2), pp. 31-41. doi: 10.21608/eajbsz.2019.36226
Hassan, H., Sayed, A. Anti-Tumor Effect of Cicer Arietinum against the Triple-Negative Breast Cancer Cells. EKB Journal Management System, 2019; 11(2): 31-41. doi: 10.21608/eajbsz.2019.36226

Anti-Tumor Effect of Cicer Arietinum against the Triple-Negative Breast Cancer Cells

Egyptian Academic Journal of Biological Sciences, B. Zoology
Article 3, Volume 11, Issue 2, May 2019, Page 31-41  XML PDF (1.06 MB)
Document Type: Original Article
DOI: 10.21608/eajbsz.2019.36226
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Authors
Hebatallah Hassan; Amany Ahmed Sayed
1-Department of Zoology, Faculty of Science, Cairo University, Giza, 12613, Egypt. 2- Structural Biology Laboratory, Egypt Nanotechnology Center (EGNC), Cairo University, El-Sheikh Zayed Campus, Zayed City, Giza, Egypt.
Abstract
Triple negative breast cancer (TNBC) is the most aggressive and deadly subtype of breast cancer. The only treatment option available for TNBC is conventional therapy, which associated with debilitating-side effects and drug-resistance. Therefore, using natural chemo-preventive agents to suppress cancer progression or reverse its initiation is an effective and safe way in cancer therapy. The aim of this study was to investigate the antitumor effect of Cicer arietinum (CAE) in vitro employing TNBC cell lines MDA-MB-231 and 4T1. Cell viability, Colony formation as readout for single cell ability to form a colony, gelatin-cell adhesion, and immunofluorescence staining were used to assessthat effect. Relative to control cells, our results indicate that CAE treatment significantly decreased cell viability, colony formation, and cell adhesion. Intriguingly, immunofluorescence microscopy unveiled that TNBC cells exhibited an attenuation of the constitutive and EGF-induced p44/42 MAPK signaling pathway implicated in regulating cell survival. Moreover, a morphological transition of TNBC cells from a fibroblast-like spindle-shaped into epithelial-like cells was observed. In conclusion, CAE may emerge as a promising antitumor agent against TNBC possibly via attenuation of EGF-induced p44/42 MAPK signaling.
Keywords
S Breast cancer; Cicer arietinum; p44/42MAPK
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