Evidence map›Paper›PMID 23179790›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2012

Interpretation of interlocking key issues of cancer stem cells in malignant solid tumors.

Wei-Hui Liu, Nan You, Ning Zhang, Hong-Tao Yan, Tao Wang, Zhu Huang, Hong-Bao Liu, Li-Jun Tang

Abstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. The cancer genome: from structure to function.Cellular oncology (Dordrecht, Netherlands) · 2014
    Article
  5. Lung cancer stem cells: a biological and clinical perspective.Cellular oncology (Dordrecht, Netherlands) · 2013
    Review
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

8 authors.

Wei-Hui LiuPLA Center of General Surgery, General Hospital of Chengdu Army Region, Chengdu, Sichuan Province, China.
Nan You
Ning Zhang
Hong-Tao Yan
Tao Wang
Zhu Huang
Hong-Bao Liu
Li-Jun Tang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn this review, several interlinking issues related to cancer stem cells (CSCs) in malignant solid tumors are sequentially discussed.

methodsA literature search was performed using PubMed, Web of Science and the Cochrane library, combining the words CSCs, solid tumor, isolation, identification, origination, therapy, target and epithelial-mesenchymal transition.

resultsBecause a primary problem is the isolation of CSCs, we first analyzed the advantages and disadvantages of recently used methods, which were mostly based on the physical or immunochemical characteristics of CSCs. Once CSCs are isolated, they should be identified by their stem cell properties. Here, we suggest how to establish a standard identification strategy. We also focused on the origination hypotheses of CSCs. The supporting molecular mechanisms for each theory were thoroughly analyzed and integrated. Especially, epithelial- mesenchymal transition is an increasingly recognized mechanism to generate CSCs that are endowed with a more invasive and metastatic phenotype. Finally, we discuss putative strategies of eliminating CSCs as effective cancer therapies.

conclusionAfter several interlocking issues of CSCs are thoroughly clarified, these CSCs in solid malignant tumors may specifically be targeted, which raises a new hope for eliminating these tumors.

Indexed as

AnimalsCell SeparationEpithelial-Mesenchymal TransitionHumansNeoplasmsNeoplastic Stem Cells

Identifiers

PMID23179790
PMCPMC12994972

What OpenQuestion holds

Textmetadata
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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.