Evidence map›Paper›PMID 22179046›Full record

ArticleNature cell biology2011

Reprogramming of the tumour microenvironment by stromal PTEN-regulated miR-320.

A Bronisz, J Godlewski, J A Wallace, A S Merchant, M O Nowicki, H Mathsyaraja, R Srinivasan, A J Trimboli, C K Martin, F Li and 16 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

170 citing papers in PubMed, 267 citations in OpenAlex.

  1. The cross-talk between GSK-3β, RKIP, and PTEN as potential targets for therapeutic implications in cancer: a comprehensive insight.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
  2. Circulating microRNAs Expression as Prognosis Biomarker of Cholangiocarcinoma.Asian Pacific journal of cancer prevention : APJCP · 2026
    Article
  3. Article
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  5. Article
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  7. [Tumor-associated fibroblasts promotes proliferation and migration of prostate cancer cells by suppressing FBXL3Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
  8. Regulatory role of RNA-binding proteins in microRNA biogenesis.Frontiers in molecular biosciences · 2024
    Review
  9. Article
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  12. Article
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  15. Article
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  18. Breast Cancer CAFs: Spectrum of Phenotypes and Promising Targeting Avenues.International journal of molecular sciences · 2021
    Review
  19. Article
  20. Review

110 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 5 institutions in 2 countries.

A BroniszTumor Microenvironment Program, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio 43210, USA.
J Godlewski
J A Wallace
A S Merchant
M O Nowicki
H Mathsyaraja
R Srinivasan
A J Trimboli
C K Martin
F Li
L Yu
S A Fernandez
T Pécot
T J Rosol
S Cory
M Hallett
M Park
M G Piper
C B Marsh
L D Yee
R E Jimenez
G Nuovo
S E Lawler
E A Chiocca
G Leone
M C Ostrowski
The Ohio State University · USMcGill University · CAThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USThe Ohio State University Wexner Medical Center · USMayo Clinic · US

Funding

Suppression of Mammary Tumorigenesis by Stromal p53P01CA097189 · NCI · OHIO STATE UNIVERSITY · PI FERNANDEZ, SOLEDAD A · 2004 to 2016
$16.1M
RAS ONCOGENE-ACTIVATED GENE EXPRESSIONR01CA053271 · NCI · OHIO STATE UNIVERSITY · PI OSTROWSKI, MICHAEL C. · 1991 to 2011
$2.9M
E2F3 and embryonic developmentR01HD047470 · NICHD · OHIO STATE UNIVERSITY · PI LEONE, GUSTAVO WALTER · 2004 to 2008
$1.6M
E2F3 GENE LOCUS IN THE CONTROL OF CELL PROLIFERATIONR01CA085619 · NCI · OHIO STATE UNIVERSITY · PI LEONE, GUSTAVO WALTER · 2001 to 2005
$1.4M
NCI NIH HHS P01 CA097189NCI NIH HHS P01CA097189NCI NIH HHS R01 CA053271NCI NIH HHS R01CA053271NCI NIH HHS R01 CA085619NCI NIH HHS R01CA85619NICHD NIH HHS R01 HD047470NICHD NIH HHS R01HD47470
6 · The paper itself

Abstract

PTEN (Phosphatase and tensin homolog deleted on chromosome 10) expression in stromal fibroblasts suppresses epithelial mammary tumours, but the underlying molecular mechanisms remain unknown. Using proteomic and expression profiling, we show that Pten loss from mammary stromal fibroblasts activates an oncogenic secretome that orchestrates the transcriptional reprogramming of other cell types in the microenvironment. Downregulation of miR-320 and upregulation of one of its direct targets, ETS2 (v-ets erythroblastosis virus E26 oncogene homolog 2) are critical events in Pten-deleted stromal fibroblasts responsible for inducing this oncogenic secretome, which in turn promotes tumour angiogenesis and tumour-cell invasion. Expression of the Pten-miR-320-Ets2-regulated secretome distinguished human normal breast stroma from tumour stroma and robustly correlated with recurrence in breast cancer patients. This work reveals miR-320 as a critical component of the Pten tumour-suppressor axis that acts in stromal fibroblasts to reprogramme the tumour microenvironment and curtail tumour progression.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticAnimalsBlotting, WesternBreast NeoplasmsCell Line, TumorChlorocebus aethiopsCOS CellsFemaleFibroblastsHumansKaplan-Meier EstimateMammary Neoplasms, ExperimentalMiceMice, KnockoutMicroRNAsEts2 protein, mouseMicroRNAsMirn320 microRNA, mouseProto-Oncogene Protein c-ets-2PTEN Phosphohydrolase

Identifiers

PMID22179046
PMCPMC3271169
OpenAlexW2028718288

What OpenQuestion holds

Textmetadata
LicenceTDM
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.