Evidence map›Paper›PMID 29485619›Full record

ArticleNutrients2018

Resveratrol and Pterostilbene Exhibit Anticancer Properties Involving the Downregulation of HPV Oncoprotein E6 in Cervical Cancer Cells.

Kaushiki Chatterjee, Dina AlSharif, Christina Mazza, Palwasha Syar, Mohamed Al Sharif, Jimmie E Fata

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 74 citations in OpenAlex.

  1. O-methylation of phenolic natural products: translational insights from resveratrol.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
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  2. Article
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  5. Pterostilbene as a promising natural anticancer agent in gynecological cancers.Medical oncology (Northwood, London, England) · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Kaushiki ChatterjeeDoctoral Program in Biology, CUNY Graduate Center, New York, NY 10016, USA. kaushiki.chatterjee@csi.cuny.edu.
Dina AlSharifDepartment of Biology, College of Staten Island, New York, NY 10314, USA. dina95usa@aol.com.
Christina MazzaDepartment of Biology, College of Staten Island, New York, NY 10314, USA. Christinamazza19@gmail.com.ORCID 0000-0002-3119-1407
Palwasha SyarDepartment of Biology, College of Staten Island, New York, NY 10314, USA. palwashasyar@yahoo.com.
Mohamed Al SharifDepartment of Biology, College of Staten Island, New York, NY 10314, USA. Alsharif.mohamed@hotmail.com.
Jimmie E FataDoctoral Program in Biology, CUNY Graduate Center, New York, NY 10016, USA. jimmie.fata@csi.cuny.edu.
College of Staten Island · USThe Graduate Center, CUNY · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer is one of the most common cancers in women living in developing countries. Due to a lack of affordable effective therapy, research into alternative anticancer compounds with low toxicity such as dietary polyphenols has continued. Our aim is to determine whether two structurally similar plant polyphenols, resveratrol and pterostilbene, exhibit anticancer and anti-HPV (Human papillomavirus) activity against cervical cancer cells. To determine anticancer activity, extensive in vitro analyses were performed. Anti-HPV activity, through measuring E6 protein levels, subsequent downstream p53 effects, and caspase-3 activation, were studied to understand a possible mechanism of action. Both polyphenols are effective agents in targeting cervical cancer cells, having low IC50 values in the µM range. They decrease clonogenic survival, reduce cell migration, arrest cells at the S-phase, and reduce the number of mitotic cells. These findings were significant, with pterostilbene often being more effective than resveratrol. Resveratrol and to a greater extent pterostilbene downregulates the HPV oncoprotein E6, induces caspase-3 activation, and upregulates p53 protein levels. Results point to a mechanism that may involve the downregulation of the HPV E6 oncoprotein, activation of apoptotic pathways, and re-establishment of functional p53 protein, with pterostilbene showing greater efficacy than resveratrol.

Indexed as

Antineoplastic AgentsApoptosisCaspase 3Cell Cycle CheckpointsDNA-Binding ProteinsDown-RegulationFemaleHeLa CellsHumansInhibitory Concentration 50Oncogene Proteins, ViralPolyphenolsRepressor ProteinsResveratrolStilbenesTumor Suppressor Protein p53Antineoplastic AgentsCASP3 protein, humanCaspase 3DNA-Binding ProteinsE6 protein, Human papillomavirus type 16E6 protein, Human papillomavirus type 18Oncogene Proteins, ViralPolyphenolspterostilbeneRepressor ProteinsResveratrolStilbenesTP53 protein, humanTumor Suppressor Protein p53cell cyclecervical cancerHPV E6p53pterostilbeneresveratrol

Identifiers

PMID29485619
PMCPMC5852819
OpenAlexW2789610044

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.