Evidence map›Paper›PMID 29922594›Full record

ReviewFrontiers in oncology2018

Cancer Stem Cell Metabolism and Potential Therapeutic Targets.

Vusala Snyder, Tamika C Reed-Newman, Levi Arnold, Sufi Mary Thomas, Shrikant Anant

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
9.1field-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

128 citing papers in PubMed, 204 citations in OpenAlex.

  1. Review
  2. Article
  3. Metabolic reprogramming and plasticity of cancer stem cells.Frontiers in cell and developmental biology · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
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  13. Review
  14. Article
  15. Article
  16. Article
  17. ExploitingInternational journal of molecular sciences · 2024
    Article
  18. Article
  19. Review
  20. Review

68 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

5 authors at 1 institution in 1 country.

Vusala SnyderDepartment of Otolaryngology, University of Kansas Medical Center, Kansas City, KS, United States.
Tamika C Reed-NewmanDepartment of General Surgery, University of Kansas Medical Center, Kansas City, KS, United States.
Levi ArnoldDepartment of Otolaryngology, University of Kansas Medical Center, Kansas City, KS, United States.
Sufi Mary ThomasDepartment of Otolaryngology, University of Kansas Medical Center, Kansas City, KS, United States.
Shrikant AnantDepartment of General Surgery, University of Kansas Medical Center, Kansas City, KS, United States.
University of Kansas Medical Center · US

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NICOLE L NOLLEN · 2012 to 2026
$40.1M
Heartland Institute for Clinical and Translational ResearchUL1TR000001 · NCATS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BAROHN, RICHARD J. · 2012 to 2015
$13.0M
HEARTLAND INSTITUTE FOR CLINICAL AND TRANSLATIONAL RESEARCHUL1RR033179 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BAROHN, RICHARD J. · 2011 to 2011
$3.2M
Bitter Melon Component and Colon Cancer PreventionR01CA190291 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ANANT, SHRIKANT, UMAR, SHAHID · 2014 to 2018
$2.7M
Dietary Prevention of CancerR01CA109269 · NCI · WASHINGTON UNIVERSITY · PI ANANT, SHRIKANT · 2005 to 2013
$2.7M
Role of autophagy in the tumor microenvironmentR01CA227838 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI THOMAS, SUFI MARY · 2019 to 2023
$1.9M
RNA Binding Proteins in CancerR01CA135559 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI ANANT, SHRIKANT · 2009 to 2013
$1.5M
NCATS NIH HHS UL1 TR000001NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA109269NCI NIH HHS R01 CA135559NCI NIH HHS R01 CA190291NCI NIH HHS R01 CA227838NCRR NIH HHS UL1 RR033179
6 · The paper itself

Abstract

Malignant tumors contain heterogeneous populations of cells in various states of proliferation and differentiation. The presence of cancer stem or initiating cells is a well-established concept wherein quiescent and poorly differentiated cells within a tumor mass contribute to drug resistance, and under permissive conditions, are responsible for tumor recurrence and metastasis. A number of studies have identified molecular markers that are characteristic of tissue-specific cancer stem cells (CSCs). Isolation of CSCs has enabled studies on the metabolic status of CSCs. As metabolic plasticity is a hallmark of cancer cell adaptation, the intricacies of CSC metabolism and their phenotypic behavior are critical areas of research. Unlike normal stem cells, which rely heavily on oxidative phosphorylation (OXPHOS) as their primary source of energy, or cancer cells, which are primarily glycolytic, CSCs demonstrate a unique metabolic flexibility. CSCs can switch between OXPHOS and glycolysis in the presence of oxygen to maintain homeostasis and, thereby, promote tumor growth. Here, we review key factors that impact CSC metabolic phenotype including heterogeneity of CSCs across different histologic tumor types, tissue-specific variations, tumor microenvironment, and CSC niche. Furthermore, we discuss how targeting key players of glycolytic and mitochondrial pathways has shown promising results in cancer eradication and attenuation of disease recurrence in preclinical models. In addition, we highlight studies on other potential therapeutic targets including complex interactions within the microenvironment and cellular communications in the CSC niche to interfere with CSC growth, resistance, and metastasis.

Indexed as

cancer stem cell markersmetabolismmicroenvironmentstem cellstargets

Identifiers

PMID29922594
PMCPMC5996058
OpenAlexW2807575739

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.