Evidence map›Paper›PMID 22560078›Full record

ArticleCell stem cell2012

The PSA(-/lo) prostate cancer cell population harbors self-renewing long-term tumor-propagating cells that resist castration.

Jichao Qin, Xin Liu, Brian Laffin, Xin Chen, Grace Choy, Collene R Jeter, Tammy Calhoun-Davis, Hangwen Li, Ganesh S Palapattu, Shen Pang and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 207 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
207citing papers in PubMed, 1 pooled it
26.1field-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

207 citing papers in PubMed, 1 synthesis or guideline pooled it, 319 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 9 institutions in 2 countries.

Jichao QinDepartment of Molecular Carcinogenesis, University of Texas M.D. Anderson Cancer Center, Science Park, Smithville, TX 78957, USA.
Xin Liu
Brian Laffin
Xin Chen
Grace Choy
Collene R Jeter
Tammy Calhoun-Davis
Hangwen Li
Ganesh S Palapattu
Shen Pang
Kevin Lin
Jiaoti Huang
Ivan Ivanov
Wei Li
Mahipal V Suraneni
Dean G Tang
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · USMethodist Hospital · USShanghai East Hospital · CNTexas A&M University · USThe University of Texas at Austin · USTongji Hospital · CNUCLA Medical Center · USUniversity of California, Los Angeles · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
Nucleotide Regulation of Apaf-1 Apoptosome and ApoptosisR01ES015888 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TANG, DEAN G. · 2007 to 2010
$1.3M
Genome-wide association study of cutaneous squamous cell carincomaR01CA166672 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI ASGARI, MARYAM MANDANA · 2013 to 2016
$1.3M
Regulation of PCa Stem/Progenitor Cells and Tumor Development by miR-34aR21CA150009 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TANG, DEAN G. · 2010 to 2011
$372k
NCI NIH HHS 1R21CA 150009NCI NIH HHS 5 P30 CA166672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA166672NCI NIH HHS R21 CA150009NIEHS NIH HHS ES007784NIEHS NIH HHS P30 ES007784NIEHS NIH HHS R01 ES015888NIEHS NIH HHS R01-ES015888
6 · The paper itself

Abstract

Prostate cancer (PCa) is heterogeneous and contains both differentiated and undifferentiated tumor cells, but the relative functional contribution of these two cell populations remains unclear. Here we report distinct molecular, cellular, and tumor-propagating properties of PCa cells that express high (PSA(+)) and low (PSA(-/lo)) levels of the differentiation marker PSA. PSA(-/lo) PCa cells are quiescent and refractory to stresses including androgen deprivation, exhibit high clonogenic potential, and possess long-term tumor-propagating capacity. They preferentially express stem cell genes and can undergo asymmetric cell division to generate PSA(+) cells. Importantly, PSA(-/lo) PCa cells can initiate robust tumor development and resist androgen ablation in castrated hosts, and they harbor highly tumorigenic castration-resistant PCa cells that can be prospectively enriched using ALDH(+)CD44(+)α2β1(+) phenotype. In contrast, PSA(+) PCa cells possess more limited tumor-propagating capacity, undergo symmetric division, and are sensitive to castration. Altogether, our study suggests that PSA(-/lo) cells may represent a critical source of castration-resistant PCa cells.

Indexed as

AdenocarcinomaAnimalsAntigens, DifferentiationAsymmetric Cell DivisionCastrationCell DifferentiationCell Line, TumorCell SurvivalCell Transformation, NeoplasticHumansMaleMiceMice, NudeMice, SCIDNeoplasm TransplantationNeoplastic Stem CellsAntigens, DifferentiationProstate-Specific Antigen

Identifiers

PMID22560078
PMCPMC3348510
OpenAlexW2066235353

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.