Evidence map›Paper›PMID 24933439›Full record

ReviewCytokine & growth factor reviews2015

Eph receptor tyrosine kinases in cancer stem cells.

Jin Chen, Wenqiang Song, Katherine Amato

Open access · greenAbstract readReview
In one paragraph

Review in Cytokine & growth factor reviews, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Eph Receptors in Cancer.Biomedicines · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Antibody Targeting of Eph Receptors in Cancer.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  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

3 authors at 2 institutions in 1 country.

Jin ChenVeterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, TN 37212, United States; Division of Rheumatology and Immunology, Department of Medicine; Department of Cancer Biology; Department of Cell and Developmental Biology; Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, TN 37232, United States. Electronic address: jin.chen@vanderbilt.edu.
Wenqiang SongVeterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, TN 37212, United States; Division of Rheumatology and Immunology, Department of Medicine.
Katherine AmatoDepartment of Cancer Biology.
Center for Rheumatology · USVA Tennessee Valley Healthcare System · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
Ephrin-A1 in Tumor-Endothelial Interaction During MetastasisR01CA095004 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CHEN, JIN · 2003 to 2019
$4.6M
ephrin-A1 in lipogenesis and breast cancer metastatic progressionR01CA177681 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRANTLEY-SIEDERS, DANA M, CHEN, JIN · 2014 to 2019
$1.9M
Targeting EphA2 in Tyrosine Kinase Inhibitor Resistant Lung CancerF31CA167878 · NCI · VANDERBILT UNIVERSITY · PI HASTINGS, KATHERINE RENEE AMATO · 2012 to 2014
$77k
Targeting mTORC2 in lung squamous cancerI01BX000134 · VA · VETERANS HEALTH ADMINISTRATION · PI Jin Chen · 2009 to 2026
–
BLRD VA I01 BX000134NCI NIH HHS F-31 CA167878NCI NIH HHS F31 CA167878NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA095004NCI NIH HHS R01 CA177681NCI NIH HHS R01 CA95004NCI NIH HHS T32 CA009592
6 · The paper itself

Abstract

Eph receptor tyrosine kinases (RTKs) and their ligands, ephrins, play critical roles in development, tissue homeostasis, and cancer. Because Eph receptors are expressed in most adult stem cell niches and in many types of cancers, it has been long suspected that this family of RTKs may also regulate the function of cancer stem-like cells (CSCs). This review will focus on recent studies to elucidate the contribution of Eph/ephrin molecules in CSC self-renewal and tumorigenicity, as well as describe efforts to target these molecules in cancer. Because CSCs are often resistant to therapeutic intervention and have been shown to depend on Eph RTKs for self-renewal, targeting Eph receptors may hold promise for the treatment of drug-resistant cancers.

Indexed as

AnimalsCell DivisionEphrinsHomeostasisHumansMiceMolecular Targeted TherapyNeoplasmsNeoplastic Stem CellsReceptors, Eph FamilySignal TransductionEphrinsReceptors, Eph FamilyCancer stem cellsEphrinEph RTK

Identifiers

PMID24933439
PMCPMC4234705
OpenAlexW1997491397

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.