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An <i>in vitro</i> investigation of the apoptosis-inducing activity of corosolic acid in breast cancer cells.

Saade Abdalkareem JasimMedical Laboratory Techniques Department, Al-Maarif University College, Al-anbar-Ramadi, IraqOmer Zedan KhalafAl-Anbar Health Directorate, IraqShadia Hamoud AlshahraniMedical Surgical Nursing Department, King Khalid University, Almahala, Abha, Saudi ArabiaKadda HachemLaboratory of Biotoxicology, Pharmacognosy and Biological Valorization of Plants (LBPVBP), Faculty of Sciences, University of Saida-Dr Moulay Tahar, 20000 Saida, AlgeriaShukhrat ZiyadullaevDepartment of Internal Diseases, Vice-rector for Scientific Affairs and Innovations, Samarkand State Medical University, Amir Temur Street 18, Samarkand, UzbekistanAbduladheem Turki JalilMedical Laboratories Techniques Department, Al-Mustaqbal University College, Babylon, Hilla, 51001, IraqChangming WangInternational College, Krirk University, Bangkok, 3 Ram Inthra Rd, Khwaeng Anusawari, Khet Bang Khen, Krung Thep Maha Nakhon, 10220, ThailandRahman S. ZabibahMedical Laboratory Technology Department, College of Medical Technology, Islamic University, Najaf, IraqYousef A. Bin JardanDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi ArabiaQutaiba A. QasimCollege of Pharmacy, Al-Ayen University, Thi-Qar, IraqMarwah Suliman MaashiMedical Laboratory Science Department, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi ArabiaYasser Fakri MustafaDepartment of Pharmaceutical Chemistry, College of Pharmacy, University of Mosul, Mosul-41001, Iraq
PubMedrepository2023en
ABI

Аннотация

Objectives: Breast cancer is the most prevalent cancer among females with different molecular subtypes. Corosolic acid is a pentacyclic triterpenoid with anti-cancer properties. Materials and Methods: The MTT assay was used to assess the cytotoxic activity of corosolic acid on MDA-MB-231 and MCF7 cell lines. To determine the apoptotic cells, the flow cytometry technique was utilized. The expression levels of apoptosis-related genes and proteins were quantified using quantitative real time-PCR (qRT-PCR) and Western blotting methods. The activity of caspase enzymes was measured by spectrophotometry. Results: Corosolic acid significantly inhibited the proliferation of both cell lines compared with controls. This agent markedly induced apoptosis in MDA-MB-231 cells but did not affect MCF7 cells compared with controls. Treating the MADA-MB-231 and MCF7 cell lines with corosolic acid showed an inducing effect on apoptosis-associated caspases, including Caspase-8, 9, and -3, in MADA-MB-231 cells with no effect on apoptotic markers in MCF7 cells. Further experiments uncovered corosolic acid-induced apoptosis in MADA-MB-231 cells by decreasing the expression of the phosphorylated form of JAK2 and STAT3 proteins. Conclusion: The present data suggested that corosolic acid is an apoptosis-inducing phytochemical in triple-negative breast cancer MADA-MB-231 cells. Also, corosolic acid triggered apoptosis in these cells by stimulating both pathways of apoptosis and inhibiting the JAK/STAT signaling. Furthermore, corosolic acid was found to inhibit MCF7 cell proliferation by a non-apoptotic mechanism.

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