Evidence map›Paper›PMID 17183365›Full record

ArticleThe EMBO journal2007

Control of prostate cell growth: BMP antagonizes androgen mitogenic activity with incorporation of MAPK signals in Smad1.

Tao Qiu, William E Grizzle, Denise K Oelschlager, Xing Shen, Xu Cao

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

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  17. Sustained BMP signaling in osteoblasts stimulates bone formation by promoting angiogenesis and osteoblast differentiation.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2009
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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

5 authors at 1 institution in 1 country.

Tao QiuDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
William E Grizzle
Denise K Oelschlager
Xing Shen
Xu Cao
University of Alabama at Birmingham · US

Funding

BIOMARKER VALIDATION LABORATORIESU24CA086359 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GRIZZLE, WILLIAM E. · 2000 to 2010
$5.1M
Smad6/7 as Sex Steroid Hormone Receptor CorepressorsR01DK060913 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CAO, XU · 2002 to 2005
$1.0M
NCI NIH HHS CA086359-07NCI NIH HHS U24 CA086359NIDDK NIH HHS DK60913NIDDK NIH HHS R01 DK060913
6 · The paper itself

Abstract

Alterations in the signaling pathways of bone morphogenetic proteins (BMPs) and activation of the ERK/MAP kinase (MAPK) pathway by growth factors have been implicated in the development and progression of prostate cancer. Smad1 acts as a substrate for MAPKs and also performs a central role in transmitting signals from BMPs. We found that BMPs/Smad1 signaling inhibits the growth of androgen-sensitive prostate cancer cells. Upon the incorporation of ERK/MAPK signals at its linker region, Smad1 physically interacts with androgen-activated androgen receptor (AR) and suppresses its functions. BMPs induce the function of Smad1 as an AR transcriptional corepressor. We demonstrated in vivo that Smad1 signaling is low in androgen-regulated growth of prostate cancer, is activated after castration, and also is decreased in hormone-independent tumors. The activation status of ERK/MAPK parallels Smad1 in the progression of prostate cancer; thus, our findings indicate a molecular basis for the integration of signals of MAPK and Smad1 in the progression and androgen regulation of prostate cancer.

Indexed as

Cell ProliferationAdenocarcinomaAndrogensAnimalsBone Morphogenetic ProteinsCells, CulturedHumansMaleMiceMitogen-Activated Protein KinasesModels, BiologicalProstateProstatic NeoplasmsReceptors, AndrogenSignal TransductionSmad1 ProteinAndrogensBone Morphogenetic ProteinsMitogen-Activated Protein KinasesReceptors, AndrogenSmad1 ProteinSMAD1 protein, human

Identifiers

PMID17183365
PMCPMC1783451
OpenAlexW2105151791

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.