Evidence map›Paper›PMID 29747682›Full record

ReviewJournal of hematology & oncology2018

The biology and role of CD44 in cancer progression: therapeutic implications.

Chen Chen, Shujie Zhao, Anand Karnad, James W Freeman

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 750 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
750citing papers in PubMed, 1 pooled it
48.6field-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.

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

750 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,410 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Encoding Cell-Surface Receptor Function Through Glycosylation: Lessons From CD44.Chembiochem : a European journal of chemical biology · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Head and neck squamous cell carcinoma: current and emerging therapeutic strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  8. Article
  9. Plasma proteomic profiling in dogs with pheochromocytoma.Journal of veterinary internal medicine · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
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  16. Article
  17. Article
  18. Review
  19. Modulation ofInternational journal of molecular sciences · 2026
    Article
  20. Review

690 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 1 institution in 1 country.

Chen ChenDepartment of Cell Systems & Atanomy, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Shujie ZhaoDepartment of Medicine, Division of Hematology and Oncology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Anand KarnadDepartment of Medicine, Division of Hematology and Oncology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
James W FreemanDepartment of Cell Systems & Atanomy, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA. freemanjw@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
NCI NIH HHS P30 CA054174
6 · The paper itself

Abstract

CD44, a non-kinase transmembrane glycoprotein, is overexpressed in several cell types including cancer stem cells and frequently shows alternative spliced variants that are thought to play a role in cancer development and progression. Hyaluronan, the main ligand for CD44, binds to and activates CD44 resulting in activation of cell signaling pathways that induces cell proliferation, increases cell survival, modulates cytoskeletal changes, and enhances cellular motility. The different functional roles of CD44 standard (CD44s) and specific CD44 variant (CD44v) isoforms are not fully understood. CD44v contain additional peptide motifs that can interact with and sequester growth factors and cytokines at the cell surface thereby functioning as coreceptors to facilitate cell signaling. Moreover, CD44v were expressed in metastasized tumors, whereas switching between CD44v and CD44s may play a role in regulating epithelial to mesenchymal transition (EMT) and in the adaptive plasticity of cancer cells. Here, we review current data on the structural and functional properties of CD44, the known roles for CD44 in tumorigencity, the regulation of CD44 expression, and the potential for targeting CD44 for cancer therapy.

Indexed as

Disease ProgressionEpithelial-Mesenchymal TransitionHumansHyaluronan ReceptorsSignal TransductionCD44 protein, humanHyaluronan ReceptorsCancerCancer therapyCD44Epithelial to mesenchymal transition (EMT)Signaling transductionTumorigenicity

Identifiers

PMID29747682
PMCPMC5946470
OpenAlexW2806713886

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.