Evidence map›Paper›PMID 24871471›Full record

ReviewThe American journal of clinical nutrition2014

Genistein inhibits human prostate cancer cell detachment, invasion, and metastasis.

Janet M Pavese, Sankar N Krishna, Raymond C Bergan

Open access · bronzeAbstract readReview
In one paragraph

Review in The American journal of clinical nutrition, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
6.1field-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

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 101 citations in OpenAlex.

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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

3 authors at 1 institution.

Janet M PaveseFrom the Department of Medicine (JMP, SNK, and RCB), the Robert H Lurie Cancer Center (RCB), and the Center for Molecular Innovation and Drug Discovery (RCB), Northwestern University, Chicago, IL.
Sankar N KrishnaFrom the Department of Medicine (JMP, SNK, and RCB), the Robert H Lurie Cancer Center (RCB), and the Center for Molecular Innovation and Drug Discovery (RCB), Northwestern University, Chicago, IL.
Raymond C BerganFrom the Department of Medicine (JMP, SNK, and RCB), the Robert H Lurie Cancer Center (RCB), and the Center for Molecular Innovation and Drug Discovery (RCB), Northwestern University, Chicago, IL.
Robert H. Lurie Comprehensive Cancer Center of Northwestern University

Funding

SUPPRESSIVE ROLE OF ANDROGEN RESPONSE GENE CALRETICULIN IN PROSTATE CANCERP50CA090386 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CRAWFORD, SUSAN · 2001 to 2013
$25.1M
DRUG DISCOVERY TRAINING IN AGE-RELATED DISORDERST32AG000260 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WATTERSON, DANIEL MARTIN · 1998 to 2010
$2.7M
Genistein-mediated Regulation of Prostate Cancer Cell MotilityR01CA122985 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BERGAN, RAYMOND C. · 2008 to 2012
$1.6M
NCI NIH HHS CA122985NCI NIH HHS CA90386NIA NIH HHS T32 AG000260
6 · The paper itself

Abstract

Prostate cancer (PCa) is the most commonly diagnosed cancer in men in the United States and the second leading cause of cancer death. Death is not caused by the primary tumor but rather by the formation of distinct metastatic tumors. Therefore, prevention of metastasis is of utmost importance. The natural product genistein, found in high amounts in soy products, has been implicated in preventing PCa formation and metastasis in men who consume high amounts of soy. In vitro studies and in vivo rodent models that used human PCa cells, as well as prospective human clinical trials, provide a mechanistic explanation directly supporting genistein as an antimetastatic agent. Specifically, our group showed that genistein inhibits cell detachment, protease production, cell invasion, and human PCa metastasis at concentrations achieved in humans with dietary intake. Finally, phase I and phase II clinical trials conducted by us and others showed that concentrations of genistein associated with antimetastatic efficacy in preclinical models are achievable in humans, and treatment with genistein inhibits pathways that regulate metastatic transformation in human prostate tissue.

Indexed as

AnimalsAnticarcinogenic AgentsAntineoplastic Agents, PhytogenicGenisteinGlycine maxHumansMaleNeoplasm InvasivenessProstatic NeoplasmsAnticarcinogenic AgentsAntineoplastic Agents, PhytogenicGenistein

Identifiers

PMID24871471
PMCPMC4144112
OpenAlexW2141773739

What OpenQuestion holds

Textmetadata
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.