Evidence map›Paper›PMID 36430806›Full record

ArticleInternational journal of molecular sciences2022

Polyphenon E Effects on Gene Expression in PC-3 Prostate Cancer Cells.

L Michael Carastro, Ethan J Vallebuona, Ricardo Cordova, Ashely N Gannon, Seung Joon Kim, Corrine M Costello, Ricardo A Declet-Bauzo, Nagi Kumar, Jong Y Park

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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

9 authors at 3 institutions in 2 countries.

L Michael CarastroDepartment of Chemistry, Biochemistry & Physics, College of Natural & Health Sciences, The University of Tampa, Tampa, FL 33606, USA.ORCID 0000-0003-2617-2970
Ethan J VallebuonaDepartment of Chemistry, Biochemistry & Physics, College of Natural & Health Sciences, The University of Tampa, Tampa, FL 33606, USA.ORCID 0000-0002-3153-9119
Ricardo CordovaDepartment of Chemistry, Biochemistry & Physics, College of Natural & Health Sciences, The University of Tampa, Tampa, FL 33606, USA.
Ashely N GannonDepartment of Chemistry, Biochemistry & Physics, College of Natural & Health Sciences, The University of Tampa, Tampa, FL 33606, USA.
Seung Joon KimDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Corrine M CostelloDepartment of Chemistry, Biochemistry & Physics, College of Natural & Health Sciences, The University of Tampa, Tampa, FL 33606, USA.
Ricardo A Declet-BauzoDepartment of Chemistry, Biochemistry & Physics, College of Natural & Health Sciences, The University of Tampa, Tampa, FL 33606, USA.
Nagi KumarDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL 33612, USA.
Jong Y ParkDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL 33612, USA.ORCID 0000-0002-6384-6447
University of Tampa · USMoffitt Cancer Center · USCatholic University of Korea · KR

Funding

Polyphenon Pharma. Mitsui Norin Co., Japan naThe University of Tampa Dana Grant, David Delo Research Grant, Research Innovation and Scholarly Excellence Award/David Delo Research GrantThe University of Tampa through a Dana Grant grant# GF2205The University of Tampa through a David Delo Research Grant grant# CC15201The University of Tampa through a Research and Innovation Scholarly Excellence Award/David Delo Research Grant grant# GR0028
6 · The paper itself

Abstract

Polyphenon E (Poly E) is a standardized, caffeine-free green tea extract with defined polyphenol content. Poly E is reported to confer chemoprotective activity against prostate cancer (PCa) progression in the TRAMP model of human PCa, and has shown limited activity against human PCa in human trials. The molecular mechanisms of the observed Poly E chemopreventive activity against PCa are not fully understood. We hypothesized that Poly E treatment of PCa cells induces gene expression changes, which could underpin the molecular mechanisms of the limited Poly E chemoprevention activity against PCa. PC-3 cells were cultured in complete growth media supplemented with varied Poly E concentrations for 24 h, then RNA was isolated for comparative DNA microarray (0 vs. 200 mg/L Poly E) and subsequent TaqMan qRT-PCR analyses. Microarray data for 54,613 genes were filtered for >2-fold expression level changes, with 8319 genes increased and 6176 genes decreased. Eight genes involved in key signaling or regulatory pathways were selected for qRT-PCR. Two genes increased expression significantly, MXD1 (13.98-fold; p = 0.0003) and RGS4 (21.98-fold; p = 0.0011), by qRT-PCR. MXD1 and RGS4 significantly increased gene expression in Poly E-treated PC-3 cells, and the MXD1 gene expression increases were Poly E dose-dependent.

Indexed as

CatechinProstatic NeoplasmsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsGene ExpressionHumansMalePC-3 CellsRepressor ProteinsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCatechinMXD1 protein, humanpolyphenon ERepressor ProteinsDNA microarraygene expressionMXD1polyphenon Eprostate cancerRGS4

Identifiers

PMID36430806
PMCPMC9697490
OpenAlexW4309743000

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.