Phytochemicals and bioactive compounds effective against acute myeloid leukemia: A systematic review.
Chukwuebuka EgbunaKingsley C Patrick-IwuanyanwuEugene N OnyeikeJohra KhanSantwana PalaiSandip B PatelVijaykumar K ParmarGarima KushwahaOmkar SinghJaison JeevanandamSuresh KumarasamyChukwuemelie Zedech UcheMathiyazhagan NarayananMithun RudrapalUchenna OdohIkenna ChikeokwuMihnea-Alexandru GămanKaliyaperumal SaravananJonathan C IfemejeShahira M EzzatMichael C OlisahChukwudi Jude ChikwenduKamoru A AdedokunSikiru O ImodoyeIbrahim O BelloHannington TwinomuhweziChinaza Godseill AwuchiPublished in: Food science & nutrition (2023)
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.
Keyphrases
- acute myeloid leukemia
- cell cycle arrest
- cell death
- dna repair
- histone deacetylase
- systematic review
- dna damage
- pi k akt
- allogeneic hematopoietic stem cell transplantation
- signaling pathway
- genome wide
- mental health
- big data
- gene expression
- single molecule
- meta analyses
- dna damage response
- bone marrow
- oxidative stress
- heat shock protein
- transcription factor
- heat shock
- endoplasmic reticulum stress
- risk assessment
- cell free
- heat stress
- randomized controlled trial
- radiation therapy
- copy number
- cell proliferation
- drug induced
- free survival
- human health
- drug delivery