Evidence map›Paper›PMID 30463302›Full record

ArticleNutrients2018

In Vitro Anticancer Properties of Table Grape Powder Extract (GPE) in Prostate Cancer.

Avinash Kumar, Melinee D'silva, Kshiti Dholakia, Anait S Levenson

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Grapevine as a Rich Source of Polyphenolic Compounds.Molecules (Basel, Switzerland) · 2020
    Review
  7. Article
  8. Grape (Foods (Basel, Switzerland) · 2020
    Review
  9. Review
  10. Article
  11. Article
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

4 authors at 1 institution in 1 country.

Avinash KumarArnold & Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, NY 11201, USA. avinash.kumar@liu.edu.
Melinee D'silvaArnold & Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, NY 11201, USA. melinee.dsilva@my.liu.edu.
Kshiti DholakiaArnold & Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, NY 11201, USA. kshiti.dholakia@my.liu.edu.
Anait S LevensonCollege of Veterinary Medicine, Long Island University, Brookville, NY 11548, USA. anait.levenson@liu.edu.
Long Island University · US

Funding

MTA1- targeted strategies for prostate cancer managementR15CA216070 · NCI · LONG ISLAND UNIVERSITY BROOKLYN CAMPUS · PI LEVENSON, ANAIT S · 2018 to 2020
$459k
California Table Grape Commission and NIH N/A and R15CA216070NCI NIH HHS R15 CA216070
6 · The paper itself

Abstract

Although the link between diet and cancer is complex, epidemiological data confirm that diet is a risk factor for prostate cancer and indicate a reduced prostate cancer incidence associated with a diet rich in vegetables and fruits. Because of the known protective effect of grape seed extract (GSE) against prostate cancer, we evaluated the effects of grape powder extract (GPE) on cell viability, proliferation, and metastatic capability. Importantly, we explored the possible novel mechanism of GPE through metastasis-associated protein 1 (MTA1) downregulation in prostate cancer, since our previous studies indicated resveratrol (Res)- and pterostilbene (Pter)-induced MTA1-mediated anticancer activities in prostate cancer. We found that GPE inhibited the cell viability and growth of prostate cancer cells only at high 100 μg/mL concentrations. However, at low 1.5⁻15 μg/mL concentrations, GPE significantly reduced the colony formation and wound healing capabilities of both DU145 and PC3M cells. Moreover, we found that GPE inhibited MTA1 in a dose-dependent manner in these cells, albeit with considerably less potency than Res and Pter. These results indicate that stilbenes such as Res and Pter specifically and potently inhibit MTA1 and MTA1-associated proteins compared to GPE, which contains low concentrations of Res and mainly consists of other flavonoids and anthocyanidins. Our findings support continued interest in GPE as a chemopreventive and anti-cancer agent against prostate cancer but also emphasize the unique and specific properties of stilbenes on MTA1-mediated anticancer effects on prostate cancer.

Indexed as

Antineoplastic Agents, PhytogenicCell Line, TumorCell ProliferationCell SurvivalChemopreventionColony-Forming Units AssayFlavonoidsHistone DeacetylasesHumansMalePlant ExtractsPowdersProstatic NeoplasmsRepressor ProteinsResveratrolStilbenesAntineoplastic Agents, PhytogenicFlavonoidsHistone DeacetylasesMTA1 protein, humanPlant ExtractsPowderspterostilbeneRepressor ProteinsResveratrolStilbenesTrans-Activatorsgrape powder extractMTA1prostate cancer

Identifiers

PMID30463302
PMCPMC6265725
OpenAlexW2901017409

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.