Evidence map›Paper›PMID 23598979›Full record

ReviewExperimental biology and medicine (Maywood, N.J.)2013

CD44 integrates signaling in normal stem cell, cancer stem cell and (pre)metastatic niches.

Karin Williams, Karan Motiani, Premkumar Vummidi Giridhar, Susan Kasper

Open access · greenAbstract readReview
In one paragraph

Review in Experimental biology and medicine (Maywood, N.J.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 1 pooled it
13.4field-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

117 citing papers in PubMed, 1 synthesis or guideline pooled it, 217 citations in OpenAlex.

  1. Pooled it
  2. Encoding Cell-Surface Receptor Function Through Glycosylation: Lessons From CD44.Chembiochem : a European journal of chemical biology · 2026
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  14. CD44 Marks Dormant Tumor Cells After HER2 Inhibition in Breast Cancer Cells.International journal of molecular sciences · 2025
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57 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

4 authors at 2 institutions in 1 country.

Karin WilliamsDepartment of Environmental Health, College of Medicine, University of Cincinnati, OH 45267, USA.
Karan Motiani
Premkumar Vummidi Giridhar
Susan Kasper
University of Cincinnati · USCincinnati Children's Hospital Medical Center · US

Funding

Developmental Biology of the Normal Mouse ProstateR01DK059142 · NIDDK · VANDERBILT UNIVERSITY · PI KASPER, SUSAN · 2002 to 2006
$1.5M
Development of Androgen Independent Prostate CancerR01DK060957 · NIDDK · VANDERBILT UNIVERSITY · PI KASPER, SUSAN · 2003 to 2007
$1.4M
NIDDK NIH HHS R01 DK059142NIDDK NIH HHS R01 DK060957NIDDK NIH HHS R01 DK60957
6 · The paper itself

Abstract

The stem cell niche provides a regulatory microenvironment for cells as diverse as totipotent embryonic stem cells to cancer stem cells (CSCs) which exhibit stem cell-like characteristics and have the capability of regenerating the bulk of tumor cells while maintaining self-renewal potential. The transmembrane glycoprotein CD44 is a common component of the stem cell niche and exists as a standard isoform (CD44s) and a range of variant isoforms (CD44v) generated though alternative splicing. CD44 modulates signal transduction through post-translational modifications as well as interactions with hyaluronan, extracellular matrix molecules and growth factors and their cognate receptor tyrosine kinases. While the function of CD44 in hematopoietic stem cells has been studied in considerable detail, our knowledge of CD44 function in tissue-derived stem cell niches remains limited. Here we review CD44s and CD44v in both hematopoietic and tissue-derived stem cell niches, focusing on their roles in regulating stem cell behavior including self-renewal and differentiation in addition to cell-matrix interactions and signal transduction during cell migration and tumor progression. Determining the role of CD44 and CD44v in normal stem cell, CSC and (pre)metastatic niches and elucidating their unique functions could provide tools and therapeutic strategies for treating diseases as diverse as fibrosis during injury repair to cancer progression.

Indexed as

Stem Cell NicheAmino Acid SequenceCell AdhesionCell DifferentiationCell MovementEpigenesis, GeneticHyaluronan ReceptorsMicroRNAsMolecular Sequence DataNeoplastic Stem CellsOxidative StressProtein Structure, TertiarySequence Analysis, ProteinSignal TransductionStem CellsTumor MicroenvironmentHyaluronan ReceptorsMicroRNAs

Identifiers

PMID23598979
PMCPMC11037417
OpenAlexW2051453787

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.