Evidence map›Paper›PMID 22357481›Full record

ReviewCell research2012

Understanding cancer stem cell heterogeneity and plasticity.

Dean G Tang

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Cell research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03176381 (Development of Tissue Predictors of Abiraterone Benefit in Men With mCRPC), which is not on this map. Cited by 324 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
324citing papers in PubMed, 1 pooled it
20.6field-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.

NCT03176381 completednot on this mapstarted 2017, after this paper: background citation

Development of Tissue Predictors of Abiraterone Benefit in Men With mCRPC

TypeobservationalSponsorTianjin Medical University Second HospitalRan2017 to 2023Enrolled110ConditionsMetastatic Castration-resistant Prostate Cancer
3 · Its place in the literature

Who cites it

324 citing papers in PubMed, 1 synthesis or guideline pooled it, 570 citations in OpenAlex.

  1. Pooled it
  2. CD8Cell reports. Medicine · 2026
    Review
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  16. CD44British journal of cancer · 2025
    Article
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264 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

1 author at 1 institution in 1 country.

Dean G TangDepartment of Molecular Carcinogenesis, the University of Texas M.D. Anderson Cancer Center, Science Park, 1808 Park Rd. 1C, Smithville, TX 78957, USA. dtang@mdanderson.org
The University of Texas MD Anderson Cancer Center · US

Funding

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
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 R21 CA150009NIEHS NIH HHS R01 ES015888NIEHS NIH HHS R01-ES015888
6 · The paper itself

Abstract

Heterogeneity is an omnipresent feature of mammalian cells in vitro and in vivo. It has been recently realized that even mouse and human embryonic stem cells under the best culture conditions are heterogeneous containing pluripotent as well as partially committed cells. Somatic stem cells in adult organs are also heterogeneous, containing many subpopulations of self-renewing cells with distinct regenerative capacity. The differentiated progeny of adult stem cells also retain significant developmental plasticity that can be induced by a wide variety of experimental approaches. Like normal stem cells, recent data suggest that cancer stem cells (CSCs) similarly display significant phenotypic and functional heterogeneity, and that the CSC progeny can manifest diverse plasticity. Here, I discuss CSC heterogeneity and plasticity in the context of tumor development and progression, and by comparing with normal stem cell development. Appreciation of cancer cell plasticity entails a revision to the earlier concept that only the tumorigenic subset in the tumor needs to be targeted. By understanding the interrelationship between CSCs and their differentiated progeny, we can hope to develop better therapeutic regimens that can prevent the emergence of tumor cell variants that are able to found a new tumor and distant metastases.

Indexed as

AnimalsCell DifferentiationCell ProliferationHumansNeoplasmsNeoplastic Stem CellsPhenotype

Identifiers

PMID22357481
PMCPMC3292302
OpenAlexW2046558067

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.