Evidence map›Paper›PMID 25915760›Full record

ArticlePloS one2015

Aldehyde Dehydrogenase 1 (ALDH1) Is a Potential Marker for Cancer Stem Cells in Embryonal Rhabdomyosarcoma.

Kengo Nakahata, Shuichiro Uehara, Shimpei Nishikawa, Miyoko Kawatsu, Masahiro Zenitani, Takaharu Oue, Hiroomi Okuyama

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 62 citations in OpenAlex.

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  10. Review
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  12. Cancer Stem Cell Markers in Rhabdomyosarcoma in Children.Diagnostics (Basel, Switzerland) · 2022
    Article
  13. Review
  14. Article
  15. Frontiers in molecular biosciences · 2022
    Article
  16. Article
  17. Transcriptional Silencing ofCancer discovery · 2021
    Article
  18. Article
  19. Article
  20. Article
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

7 authors at 1 institution in 1 country.

Kengo NakahataDepartments of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Shuichiro UeharaDepartments of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Shimpei NishikawaFrontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Osaka, Japan.
Miyoko KawatsuDepartments of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Masahiro ZenitaniDepartments of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Takaharu OueDepartments of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Hiroomi OkuyamaDepartments of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells (CSCs) are defined as a small population of cancer cells with the properties of high self-renewal, differentiation, and tumor-initiating functions. Recent studies have demonstrated that aldehyde dehydrogenase 1 (ALDH1) is a marker for CSCs in adult cancers. Although CSCs have been identified in some different types of pediatric solid tumors, there have been no studies regarding the efficacy of ALDH1 as a marker for CSCs. Therefore, in order to elucidate whether ALDH1 can be used as a marker for CSCs of pediatric sarcoma, we examined the characteristics of a population of cells with a high ALDH1 activity (ALDH1high cells) in rhabdomyosarcoma (RMS), the most common soft tissue sarcoma in children. We used the human embryonal RMS (eRMS) cell lines RD and KYM-1, and sorted the cells into two subpopulations of ALDH1high cells and cells with a low ALDH1 activity (ALDH1low cells). Consequently, we found that the ALDH1high cells comprised 3.9% and 8.2% of the total cell population, respectively, and showed a higher capacity for self-renewal and tumor formation than the ALDH1low cells. With regard to chemoresistance, the survival rate of the ALDH1high cells was found to be higher than that of the ALDH1low cells following treatment with chemotherapeutic agents for RMS. Furthermore, the ALDH1high cells exhibited a higher degree of pluripotency and gene expression of Sox2, which is one of the stem cell markers. Taken together, the ALDH1high cells possessed characteristics of CSCs, including colony formation, chemoresistance, differentiation and tumor initiation abilities. These results suggest that ALDH1 is a potentially useful marker of CSCs in eRMS.

Indexed as

Aldehyde Dehydrogenase 1 FamilyAnimalsAntineoplastic AgentsBiomarkers, TumorCell Line, TumorCell SurvivalColony-Forming Units AssayDrug Resistance, NeoplasmFluorescent Antibody TechniqueHumansIsoenzymesMice, Inbred NODNeoplasm TransplantationNeoplastic Stem CellsReal-Time Polymerase Chain ReactionRetinal DehydrogenaseAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, humanALDH1A1 protein, mouseAntineoplastic AgentsBiomarkers, TumorIsoenzymesRetinal Dehydrogenase

Identifiers

PMID25915760
PMCPMC4411144
OpenAlexW1978051405

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Registered trials

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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.