Evidence map›Paper›PMID 27043282›Full record

ArticleThe Journal of clinical investigation2016

SOX9 drives WNT pathway activation in prostate cancer.

Fen Ma, Huihui Ye, Housheng Hansen He, Sean J Gerrin, Sen Chen, Benjamin A Tanenbaum, Changmeng Cai, Adam G Sowalsky, Lingfeng He, Hongyun Wang and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
19.2field-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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 184 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Integration Analysis of Single-Cell Multi-Omics Reveals Prostate Cancer Heterogeneity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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37 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 1 country.

Fen Ma
Huihui Ye
Housheng Hansen He
Sean J Gerrin
Sen Chen
Benjamin A Tanenbaum
Changmeng Cai
Adam G Sowalsky
Lingfeng He
Hongyun Wang
Steven P Balk
Xin Yuan
Beth Israel Deaconess Medical Center · USHarvard University · US

Funding

Tumor and Circulating Markers as Links Between Obesity and Lethal Prostate CanceP50CA090381 · NCI · DANA-FARBER CANCER INSTITUTE · PI LODA, MASSIMO · 2002 to 2017
$36.2M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI EVA COREY · 2013 to 2026
$25.0M
SOX9 Mediation of AR and ERG Driven Prostate CancerR01CA168393 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BALK, STEVEN P., YUAN, XIN · 2014 to 2018
$1.8M
SOX9 in prostate cancer development and progressionR01DK079962 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI YUAN, XIN · 2008 to 2012
$1.8M
Molecular basis of androgen receptor mediated gene transcriptional repressionK99CA166507 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CAI, CHANGMENG · 2012 to 2013
$270k
NCI NIH HHS K99 CA166507NCI NIH HHS P01 CA163227NCI NIH HHS P50 CA090381NCI NIH HHS R01 CA168393NIDDK NIH HHS R01 DK079962
6 · The paper itself

Abstract

The transcription factor SOX9 is critical for prostate development, and dysregulation of SOX9 is implicated in prostate cancer (PCa). However, the SOX9-dependent genes and pathways involved in both normal and neoplastic prostate epithelium are largely unknown. Here, we performed SOX9 ChIP sequencing analysis and transcriptome profiling of PCa cells and determined that SOX9 positively regulates multiple WNT pathway genes, including those encoding WNT receptors (frizzled [FZD] and lipoprotein receptor-related protein [LRP] family members) and the downstream β-catenin effector TCF4. Analyses of PCa xenografts and clinical samples both revealed an association between the expression of SOX9 and WNT pathway components in PCa. Finally, treatment of SOX9-expressing PCa cells with a WNT synthesis inhibitor (LGK974) reduced WNT pathway signaling in vitro and tumor growth in murine xenograft models. Together, our data indicate that SOX9 expression drives PCa by reactivating the WNT/β-catenin signaling that mediates ductal morphogenesis in fetal prostate and define a subgroup of patients who would benefit from WNT-targeted therapy.

Indexed as

Gene Expression Regulation, NeoplasticWnt Signaling PathwayAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCell Line, TumorHumansMaleMiceMice, NudeMice, SCIDNeoplasm ProteinsProstatic NeoplasmsPyrazinesPyridinesSOX9 Transcription FactorTranscription Factor 4Basic Helix-Loop-Helix Leucine Zipper Transcription FactorsLGK974Neoplasm ProteinsPyrazinesPyridinesSOX9 protein, humanSOX9 Transcription FactorTCF4 protein, humanTranscription Factor 4Transcription Factors

Identifiers

PMID27043282
PMCPMC4855922
OpenAlexW2314502206

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.