Evidence map›Paper›PMID 40991529›Full record

ArticlePloS one2025

Antiproliferative activity of Grewia villosa ethyl acetate extract on cervical cancer HeLa cell line: Mechanistic insights through network pharmacology and functional assays approach.

Sally Wambui Kamau, Mercy Jepkorir, Gilbert Kipkoech, Inyani John Lino Lagu, Wesley Kanda, Susan Kibunja, Rakita Letoluo, Shadrack Barmasai, Alice Wanyoko, Vincent Ruttoh and 4 more

Abstract read
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Article in PloS one, 2025. 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

What it found

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2 · The registry

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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

14 authors.

Sally Wambui KamauDepartment of Biochemistry, Microbiology and Biotechnology, Kenyatta University, Nairobi, Kenya.
Mercy JepkorirCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Gilbert KipkoechDepartment of Biochemistry, Microbiology and Biotechnology, Kenyatta University, Nairobi, Kenya.
Inyani John Lino LaguPan African Union Institute for Basic Science and Technology (PAUSTI), Nairobi, Kenya.
Wesley KandaCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Susan KibunjaDepartment of Biochemistry, Microbiology and Biotechnology, Kenyatta University, Nairobi, Kenya.
Rakita LetoluoCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Shadrack BarmasaiCentre for Virus Research (CVR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Alice WanyokoCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Vincent RuttohCentre for Virus Research (CVR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
James KuriaCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Peter Githaiga MwitariCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Mathew Piero NgugiDepartment of Biochemistry, Microbiology and Biotechnology, Kenyatta University, Nairobi, Kenya.
Sospeter Ngoci NjeruCentre for Traditional Medicine and Drug Research (CTMDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.ORCID 0000-0003-1154-0777

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Grewia villosa is a plant native to Kenya, with a traditional history among Ambeere people for treating and managing prostate and breast cancers. Previous scientific studies have demonstrated its anti-inflammatory and antioxidant properties. However, a scientific gap exists on the bioactivity of G. villosa against cervical cancer, particularly on in vitro HeLa cell line model. Additionally, the specific molecular targets and mode of antiproliferative action have not been well elucidated. Therefore, this study sought to investigate the antiproliferative activity, putative targets and mode of action of G. villosa using in vitro cell culture, molecular biology and in silico-based approaches. Antiproliferative analyses were evaluated through MTT assay, cell migration inhibition through in vitro scratch assay, and phytochemical profiling through Gas chromatography-mass spectrometry (GC-MS) analysis. Further, putative targets were identified through network pharmacology approach, computationally validated by molecular docking, and functionally through the real-time quantitative polymerase chain reaction (RT-qPCR) method. The G. villosa ethyl acetate (GVEA) extract fraction was the most active extract fraction, with IC50 of 100.7 µg/mL and a selectivity index of 2.38. Dodecan-2-ylbenzene and 2,6,10-trimethyltetradecane compounds were some notable compounds that can partly be associated with reported antiproliferative activity as they demonstrated strong binding affinity to identified putative targets, including EGFR and AKT1. RT-qPCR analysis functionally confirmed the downregulation of EGFR and AKT1, and the upregulation of tumor protein 53 and Caspase 3 molecular targets, suggesting that GVEA extract indeed perturbs the predicted molecular targets. This study therefore reports the selective antiproliferative properties of the G. villosa ethyl acetate extract fraction in a cervical cancer model (HeLa) cell line while at the same time providing putative targets, which is important in shedding light on potential mechanistic basis of its demonstrated antiproliferative activity. This highlights the plant's potential in discovering products and compounds for further investigation on possible application in cervical cancer management and/or treatment.

Indexed as

Antineoplastic Agents, PhytogenicCell ProliferationPlant ExtractsUterine Cervical NeoplasmsAcetatesApoptosisCell MovementFemaleHeLa CellsHumansMolecular Docking SimulationNetwork PharmacologyProto-Oncogene Proteins c-aktAcetatesAntineoplastic Agents, Phytogenicethyl acetatePlant ExtractsProto-Oncogene Proteins c-akt

Identifiers

PMID40991529
PMCPMC12459836

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.