Evidence map›Paper›PMID 23097625›Full record

ArticleNeoplasia (New York, N.Y.)2012

Role of transcriptional corepressor CtBP1 in prostate cancer progression.

Rui Wang, Irfan A Asangani, Balabhadrapatruni V S K Chakravarthi, Bushra Ateeq, Robert J Lonigro, Qi Cao, Ram-Shankar Mani, Daniel F Camacho, Natalie McGregor, Taibriana E W Schumann and 15 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.0field-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

49 citing papers in PubMed, 114 citations in OpenAlex.

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  13. Cryo-EM structure of CtBP2 confirms tetrameric architecture.Structure (London, England : 1993) · 2021
    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

25 authors at 4 institutions in 2 countries.

Rui WangMichigan Center for Translational Pathology, Department of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109-0602, USA.
Irfan A Asangani
Balabhadrapatruni V S K Chakravarthi
Bushra Ateeq
Robert J Lonigro
Qi Cao
Ram-Shankar Mani
Daniel F Camacho
Natalie McGregor
Taibriana E W Schumann
Xiaojun Jing
Radhika Menawat
Scott A Tomlins
Heng Zheng
Arie P Otte
Rohit Mehra
Javed Siddiqui
Saravana M Dhanasekaran
Mukesh K Nyati
Kenneth J Pienta
Nallasivam Palanisamy
Lakshmi P Kunju
Mark A Rubin
Arul M Chinnaiyan
Sooryanarayana Varambally
University of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · USCornell University · USUniversity of Amsterdam · NL

Funding

VACCINIA PSA FOR ANDROGEN-MODULATED POST-SURGICAL RECURRENCE OF PROSTATE CANCERP50CA069568 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M · 1995 to 2013
$31.3M
Epitomic Biomarkers of Prostate CancerU01CA111275 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, RUBIN, MARK A. · 2004 to 2015
$6.8M
Regulation of Polycomb Repressive Complex 1 by EZH2 Regulated microRNAs in CancerR01CA157845 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VARAMBALLY, SOORYANARAYANA · 2011 to 2015
$1.6M
Role of Transcriptional Corepressor CtBP1 in Prostate Cancer ProgressionR01CA154980 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VARAMBALLY, SOORYANARAYANA · 2012 to 2016
$1.5M
Tracing the origins of chromosomal translocations in prostate cancerK99CA160640 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MANI, RAM SHANKAR · 2012 to 2013
$230k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA160640NCI NIH HHS P50 CA069568NCI NIH HHS P50CA69568NCI NIH HHS PC020322NCI NIH HHS R01 CA154980NCI NIH HHS R01CA154980NCI NIH HHS R01 CA157845NCI NIH HHS R01CA157845NCI NIH HHS U01 CA111275NCI NIH HHS UO1 CA111275
6 · The paper itself

Abstract

Transcriptional repressors and corepressors play a critical role in cellular homeostasis and are frequently altered in cancer. C-terminal binding protein 1 (CtBP1), a transcriptional corepressor that regulates the expression of tumor suppressors and genes involved in cell death, is known to play a role in multiple cancers. In this study, we observed the overexpression and mislocalization of CtBP1 in metastatic prostate cancer and demonstrated the functional significance of CtBP1 in prostate cancer progression. Transient and stable knockdown of CtBP1 in prostate cancer cells inhibited their proliferation and invasion. Expression profiling studies of prostate cancer cell lines revealed that multiple tumor suppressor genes are repressed by CtBP1. Furthermore, our studies indicate a role for CtBP1 in conferring radiation resistance to prostate cancer cell lines. In vivo studies using chicken chorioallantoic membrane assay, xenograft studies, and murine metastasis models suggested a role for CtBP1 in prostate tumor growth and metastasis. Taken together, our studies demonstrated that dysregulated expression of CtBP1 plays an important role in prostate cancer progression and may serve as a viable therapeutic target.

Indexed as

ApoptosisCell ProliferationAlcohol OxidoreductasesAnimalsBlotting, WesternCell MovementChick EmbryoChorioallantoic MembraneChromatin ImmunoprecipitationDNA-Binding ProteinsGene Expression ProfilingGenes, Tumor SuppressorHumansImmunoenzyme TechniquesLung NeoplasmsMaleAlcohol OxidoreductasesC-terminal binding proteinDNA-Binding ProteinsRNA, Small Interfering

Identifiers

PMID23097625
PMCPMC3479836
OpenAlexW1207770767

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.