Evidence map›Paper›PMID 34368899›Full record

ArticleJournal of the Egyptian National Cancer Institute2021

Chloroform extract and acetyl-11-keto-beta-boswellic acid from Boswellia dalzielii stem bark induce apoptosis and cell cycle blockage in AW8507 cells.

Akinbobola Peace Otitoju, Ishaya Yohanna Longdet, Taiwo Emmanuel Alemika, Vikram Prakash Gota

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Article in Journal of the Egyptian National Cancer Institute, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Akinbobola Peace OtitojuDepartment of Biochemistry, Faculty of Basic Medical Sciences, University of Jos, Jos, Nigeria. akinbobolapeace@gmail.com.ORCID http://orcid.org/0000-0002-3226-1534
Ishaya Yohanna LongdetDepartment of Biochemistry, Faculty of Basic Medical Sciences, University of Jos, Jos, Nigeria.
Taiwo Emmanuel AlemikaDepartment of Pharmaceutical Chemistry, Faculty of Pharmaceutical Science, University of Jos, Jos, Nigeria.
Vikram Prakash GotaAdvanced Centre for Treatment Research and Education in Cancer (ACTREC), Department of Clinical Pharmacology, Tata Memorial Centre, Kharghar, Navi, Mumbai, 410210, India.
University of Jos · NGTata Memorial Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlobally, head and neck cancer is the sixth most common cancer. Despite the advancement in treatment, drug resistance remains a major cause for setback. In an earlier work, the authors reported that Boswellia dalzielii (Hutch) stem bark exhibited dose-dependent cytotoxicity in head and neck cancer cells, AW8507. Therefore, the cell death induction effect of Boswellia dalzielii stem bark chloroform extract in head and neck cancer cell line, AW8507, and its derived constituent on cell cycle and apoptosis proteins was further investigated.

methodsThe cell death induction activity of the Boswellia dalzielii stem bark chloroform fraction (CLBD) in AW8507 was determined using Annexin V-FITC/PI staining in flow cytometry. High-performance liquid chromatography-mass spectrometry was employed for compounds analysis of the CLBD, and reverse virtual screening was used to identify the mechanism of action of the compound, acetyl-11-keto-beta-boswellic acid, that was elucidated in the Boswellia dalzielii chloroform fraction.

resultsThe data obtained showed that Boswellia dalzielii stem bark Chloroform extract increased the percentage of cells presenting for early apoptosis from 4.14 to 10.10% in AW8507 cells. High-performance liquid chromatography-mass spectrometry analysis of the chloroform fraction identified acetyl-11-keto-beta-boswellic acid. Reverse virtual screening on selected proteins showed that acetyl-11-keto-beta-boswellic acid is a multi-protein target compound. It binds preferably to phosphorylated-cyclin dependent kinase 1 (p-CDK1) (binding score =  - 9.2 kcal/mol), blocking the activation of cyclin B-CDK1 needed for cell cycle progression at G2/M phase of the cell cycle. Acetyl-11-keto-beta-boswellic acid also binds more tightly with αβ tubulin (binding score = 8.9 kcal/mol) than with the standard drug, docetaxel (binding score = 8.3 kcal/mol).

conclusionsThe results obtained confirmed the culpability of Boswellia dalzielii-derived acetyl-11-keto-beta-boswellic acid in the obstruction of the cell cycle progression in head and neck cancer cell line, AW8507; and the induction of apoptosis earlier reported for Boswellia dalzielii (Hutch) stem bark. Additional in vitro and/or in vivo studies would be required to validate in silico observations.

Indexed as

BoswelliaApoptosisCell CycleCell DivisionChloroformHumansPlant BarkPlant ExtractsTriterpenesacetyl-11-ketoboswellic acidChloroformPlant ExtractsTriterpenesAcetyl-11-keto-beta-boswellic acidBoswellia dalzielii; HPLC–MSReverse virtual screening

Identifiers

PMID34368899
PMCPMC13316886
OpenAlexW3192502657

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