Chukwuebuka, Egbuna and Kingsley, C. Patrick-Iwuanyanwu and Eugene, N. Onyeike and Johra, Khan and Santwana, Palai and Sandip, B. Patel and Vijaykumar, K. Parmar and Garima, Kushwaha and Omkar, Singh and Jaison, Jeevanandam and Suresh, Kumarasamy and Chukwuemelie, Zedech Uche and Mathiyazhagan, Narayanan and Mithun, Rudrapal and Uchenna, Odoh and Ikenna, Chikeokwu and Mihnea-Alexandru, Gaman and Kaliyaperumal, Saravanan and Jonathan, C. Ifemeje and Shahira, M. Ezzat and Michael, C. Olisah and Chukwudi Jude, Chikwendu and Kamoru, A. Adedokun and Sikiru, O. Imodoye and Ibrahim, O. Bello and Hannington, Twinomuhwez and Chinaza Godswill, Awuchi (2023) Phytochemicals and bioactive compounds effective against acute myeloid leukemia: A systematic review. Food Science and Nutrition. pp. 1-20. ISSN 20487177
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Abstract
This systematic review identified various bioactive compounds which have the potential to serve as novel drugs or leads against acute myeloid leukemia. Acute myeloid leukemia (AML) is a heterogeneous hematopoietic malignancy that arises from the dysregulation of cell differentiation, proliferation, and cell death. The risk factors associated with the onset of AML include long-term exposure to radiation and chemicals such as benzene, smoking, genetic disorders, blood disorders, advancement in age, and others. Although novel strategies to manage AML, including a refinement of the conventional chemotherapy regimens, hypomethylating agents, and molecular targeted drugs, have been developed in recent years, resistance and relapse remain the main clinical problems. In this study, three databases, PubMed/MEDLINE,
ScienceDirect, and Google Scholar, were systematically searched to identify various bioactive compounds with antileukemic properties. A total of 518 articles were identified, out of which 59 were viewed as eligible for the current report. From the data extracted, over 60 bioactive compounds were identified and divided into five major groups: flavonoids, alkaloids, organosulfur compounds, terpenes, and terpenoids, and other known and emerging bioactive compounds. The mechanism of actions of the analyzed individual bioactive molecules differs remarkably and includes disrupting chromatin structure, upregulating the synthesis of certain DNA repair proteins, inducing cell cycle arrest and apoptosis, and inhibiting/regulating Hsp90 activities, DNA methyltransferase 1, and histone deacetylase 1.
Item Type: | Article |
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Subjects: | AC Rearch Cluster |
Depositing User: | Unnamed user with email techsupport@mosys.org |
Date Deposited: | 12 Jul 2023 05:27 |
Last Modified: | 12 Jul 2023 05:27 |
URI: | https://ir.vignan.ac.in/id/eprint/204 |