Evidence map›Paper›PMID 20937021›Full record

ReviewCurrent molecular medicine2010

Defining the molecular nexus of cancer, type 2 diabetes and cardiovascular disease.

S M Cabarcas, E M Hurt, W L Farrar

Abstract readReview
In one paragraph

Review in Current molecular medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Cancer, inflammation, and insights from ayurveda.Evidence-based complementary and alternative medicine : eCAM · 2012
    Article
  10. 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.

S M CabarcasCancer Stem Cell Section, Laboratory of Cancer Prevention, Center for Cancer Research, National Cancer Institute, Frederick, Maryland 21702, USA.
E M Hurt
W L Farrar

Funding

Characterization of Cancer Stem CellsZIABC010794 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FARRAR, WILLIAM · 2009 to 2012
$3.2M
Molecular Mechanisms of Growth Factor Modulated ProliferationZIABC010253 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FARRAR, WILLIAM · 2009 to 2012
$795k
Intramural NIH HHS ZIA BC010253NCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400
6 · The paper itself

Abstract

The metabolic syndrome is characterized by a state of metabolic dysfunction resulting in the development of several chronic diseases that are potentially deadly. These metabolic deregulations are complex and intertwined and it has been observed that many of the mechanisms and pathways responsible for diseases characterizing the metabolic syndrome such as type 2 diabetes and cardiovascular disease are linked with cancer development as well. Identification of molecular pathways common to these diverse diseases may prove to be a critical factor in disease prevention and development of potential targets for therapeutic treatments. This review focuses on several molecular pathways, including AMPK, PPARs and FASN that interconnect cancer development, type 2 diabetes and cardiovascular disease. AMPK, PPARs and FASN are crucial regulators involved in the maintenance of key metabolic processes necessary for proper homeostasis. It is critical to recognize and identify common pathways deregulated in interrelated diseases as it may provide further information and a much more global picture in regards to disease development and prevention. Thus, this review focuses on three key metabolic regulators, AMPK, PPARs and FASN, that may potentially serve as therapeutic targets.

Indexed as

AMP-Activated Protein Kinase KinasesAnimalsCardiovascular DiseasesDiabetes Mellitus, Type 2Fatty Acid SynthasesHumansMetabolic SyndromeNeoplasmsPeroxisome Proliferator-Activated ReceptorsProtein KinasesRisk FactorsAMP-Activated Protein Kinase KinasesFatty Acid SynthasesPeroxisome Proliferator-Activated ReceptorsProtein Kinases

Identifiers

PMID20937021
PMCPMC3448443

What OpenQuestion holds

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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.