Evidence map›Paper›PMID 24280133›Full record

ArticleEndocrine-related cancer2014

SOCS2 correlates with malignancy and exerts growth-promoting effects in prostate cancer.

Julia Hoefer, Johann Kern, Philipp Ofer, Iris E Eder, Georg Schäfer, Dimo Dietrich, Glen Kristiansen, Stephan Geley, Johannes Rainer, Eberhard Gunsilius and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Endocrine-related cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Overexpression of SOCS2 Inhibits EMT and M2 Macrophage Polarization in Cervical CancerCombinatorial chemistry & high throughput screening · 2024
    Article
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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

13 authors at 1 institution in 2 countries.

Julia HoeferExperimental Urology, Department of Urology, Innsbruck Medical University, Anichstrasse 35, A-6020 Innsbruck, Austria Oncotyrol Laboratory for Tumor Biology and Angiogenesis, Innsbruck, Austria Institute of Pathology, University Hospital Bonn, Bonn, Germany Division of Molecular Pathophysiology, Innsbruck Biocenter, Medical University Innsbruck, Innsbruck, Austria.
Johann Kern
Philipp Ofer
Iris E Eder
Georg Schäfer
Dimo Dietrich
Glen Kristiansen
Stephan Geley
Johannes Rainer
Eberhard Gunsilius
Helmut Klocker
Zoran Culig
Martin Puhr
Innsbruck Medical University · AT

Funding

Austrian Science Fund FWF P 25639Austrian Science Fund FWF W 1101
6 · The paper itself

Abstract

Deregulation of cytokine and growth factor signaling due to an altered expression of endogenous regulators is well recognized in prostate cancer (PCa) and other cancers. Suppressor of cytokine signaling 2 (SOCS2) is a key regulator of the GH, IGF, and prolactin signaling pathways that have been implicated in carcinogenesis. In this study, we evaluated the expression patterns and functional significance of SOCS2 in PCa. Protein expression analysis employing tissue microarrays from two independent patient cohorts revealed a significantly enhanced expression in tumor tissue compared with benign tissue as well as association with Gleason score and disease progression. In vitro and in vivo assays uncovered the involvement of SOCS2 in the regulation of cell growth and apoptosis. Functionally, SOCS2 knockdown inhibited PCa cell proliferation and xenograft growth in a CAM assay. Decreased cell growth after SOCS2 downregulation was associated with cell-cycle arrest and apoptosis. In addition, we proved that SOCS2 expression is significantly elevated upon androgenic stimulation in androgen receptor (AR)-positive cell lines, providing a possible mechanistic explanation for high SOCS2 levels in PCa tissue. Consequently, SOCS2 expression correlated with AR expression in the malignant tissue of patients. On the whole, our study linked increased SOCS2 expression in PCa with a pro-proliferative role in vitro and in vivo.

Indexed as

ApoptosisCell CycleCell Line, TumorCell ProliferationHumansMaleProstateProstatic NeoplasmsReceptors, AndrogenSuppressor of Cytokine Signaling ProteinsTissue Array AnalysisTumor BurdenAR protein, humanReceptors, AndrogenSOCS2 protein, humanSuppressor of Cytokine Signaling Proteinsandrogenproliferationprostate cancerSOCS2survival

Identifiers

PMID24280133
PMCPMC3907181
OpenAlexW2098029653

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.