Evidence map›Paper›PMID 20187302›Full record

ArticleJournal of cellular and molecular medicine2009

Developmental tumourigenesis: NCAM as a putative marker for the malignant renal stem/progenitor cell population.

Naomi Pode-Shakked, Sally Metsuyanim, Eithan Rom-Gross, Yoram Mor, Eduard Fridman, Itamar Goldstein, Ninette Amariglio, Gideon Rechavi, Gilmor Keshet, Benjamin Dekel

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
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  14. CD90/Thy-1, a Cancer-Associated Cell Surface Signaling Molecule.Frontiers in cell and developmental biology · 2019
    Review
  15. Article
  16. Article
  17. Biomarker discovery for renal cancer stem cells.The journal of pathology. Clinical research · 2018
    Review
  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

10 authors at 3 institutions in 1 country.

Naomi Pode-ShakkedDepartment of Pediatrics and Pediatric Stem Cell Research Institute, Sheba Medical Center, Israel.
Sally MetsuyanimDepartment of Pediatrics and Pediatric Stem Cell Research Institute, Sheba Medical Center, Israel.
Eithan Rom-GrossDepartment of Pediatric Surgery, Hadassah Medical Center, Hebrew University, Israel.
Yoram MorDepartment of Urology, Sheba Medical Center, Israel.
Eduard FridmanDepartment of Pathology, Sheba Medical Center, Israel.
Itamar GoldsteinDepartment of Pediatric Hemato-Oncology and Sheba Cancer Research Center, Sheba Medical Center, Israel.
Ninette AmariglioDepartment of Pediatric Hemato-Oncology and Sheba Cancer Research Center, Sheba Medical Center, Israel.
Gideon RechaviDepartment of Pediatric Hemato-Oncology and Sheba Cancer Research Center, Sheba Medical Center, Israel.
Gilmor KeshetDepartment of Pediatric Hemato-Oncology and Sheba Cancer Research Center, Sheba Medical Center, Israel.
Benjamin DekelDepartment of Pediatrics and Pediatric Stem Cell Research Institute, Sheba Medical Center, Israel.
Tel Aviv University · ILSheba Medical Center · ILHadassah Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During development, renal stem cells reside in the nephrogenic blastema. Wilms' tumour (WT), a common childhood malignancy, is suggested to arise from the nephrogenic blastema that undergoes partial differentiation and as such is an attractive model to study renal stem cells leading to cancer initiation and maintenance. Previously we have made use of blastema-enriched WT stem-like xenografts propagated in vivo to define a 'WT-stem' signature set, which includes cell surface markers convenient for cell isolation (frizzled homolog 2 [Drosophila] - FZD2, FZD7, G-protein coupled receptor 39, activin receptor type 2B, neural cell adhesion molecule - NCAM). We show by fluorescenceactivated cell sorting analysis of sphere-forming heterogeneous primary WT cultures that most of these markers and other stem cell surface antigens (haematopoietic, CD133, CD34, c-Kit; mesenchymal, CD105, CD90, CD44; cancer, CD133, MDR1; hESC, CD24 and putative renal, cadherin 11), are expressed in WT cell sub-populations in varying levels. Of all markers, NCAM, CD133 and FZD7 were constantly detected in low-to-moderate portions likely to contain the stem cell fraction. Sorting according to FZD7 resulted in extensive cell death, while sorted NCAM and CD133 cell fractions were subjected to clonogenicity assays and quantitative RT-PCR analysis, exclusively demonstrating the NCAM fraction as highly clonogenic, overexpressing the WT 'stemness' genes and topoisomerase2A (TOP2A), a bad prognostic marker for WT. Moreover, treatment of WT cells with the topoisomerase inhibitors, Etoposide and Irinotecan resulted in down-regulation of TOP2A along with NCAM and WT1. Thus, we suggest NCAM as a marker for the WT progenitor cell population. These findings provide novel insights into the cellular hierarchy of WT, having possible implications for future therapeutic options.

Indexed as

Antineoplastic AgentsBiomarkers, TumorChildChild, PreschoolFemaleFlow CytometryGene ExpressionHumansImmunohistochemistryInfantKidney NeoplasmsMaleNeoplastic Stem CellsNeural Cell Adhesion MoleculesReverse Transcriptase Polymerase Chain ReactionWilms TumorAntineoplastic AgentsBiomarkers, TumorNeural Cell Adhesion Molecules

Identifiers

PMID20187302
PMCPMC6529968
OpenAlexW2043595329

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.