Evidence map›Paper›PMID 21428801›Full record

ReviewFuture medicinal chemistry2010

Targeted therapies of the LKB1/AMPK pathway for the treatment of insulin resistance.

Eijiro Yamada, Ting-Wen A Lee, Jeffrey E Pessin, Claire C Bastie

Abstract readReview
In one paragraph

Review in Future medicinal chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Antidiabetic potential of fenugreek (Food science & nutrition · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
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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.

Eijiro YamadaAlbert Einstein College of Medicine and Neuroscience, Diabetes Research and Training Center, Department of Medicine, Bronx, NY 10461, USA.
Ting-Wen A Lee
Jeffrey E Pessin
Claire C Bastie
Albert Einstein College of Medicine · USChildren's Hospital at Montefiore · US

Funding

Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI FLEISCHER, NORMAN S. · 1986 to 2014
$29.8M
REGULATION OF THE INSULIN RECEPTOR KINASER01DK033823 · NIDDK · UNIVERSITY OF IOWA · PI KURLAND, IRWIN JACK, PESSIN, JEFFREY E. · 1986 to 2022
$6.7M
Reorganization of motor cortex following brain injuryR37NS030853 · NINDS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NUDO, RANDOLPH J. · 2008 to 2014
$4.6M
FYN SRC Kinase Regulation of Fatty Acid Oxidation and Insulin SensitivityR01DK081412 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BASTIE, CLAIRE C · 2010 to 2014
$1.8M
Regulation of insulin sensitivity by the Src family non-receptor tyrosine kinase,R21DK078886 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI PESSIN, JEFFREY E. · 2007 to 2008
$438k
NIDDK NIH HHS DK078886NIDDK NIH HHS P60 DK020541NIDDK NIH HHS R01 DK033823NIDDK NIH HHS R01 DK081412NIDDK NIH HHS R21 DK078886NINDS NIH HHS R37 NS030853
6 · The paper itself

Abstract

Type II diabetes is characterized by elevated serum glucose levels and altered lipid metabolism due to peripheral insulin resistance and defects of insulin secretion in the pancreatic β-cells. While some cases of obesity and Type II diabetes result from genetic dysfunction, the increased worldwide incidence of these two disorders strongly suggest that the contribution of environmental factors such as sedentary lifestyles and high-calorie intake may disrupt energy balance. AMP-activated protein kinase and its upstream kinase liver kinase B1 are conserved serine/threonine kinases regulating anabolic and catabolic metabolic processes, therefore representing attractive therapeutic targets for the treatment of obesity and Type II diabetes. In this review, we will discuss the advantages of targeting the liver kinase B1/AMP-activated protein kinase pathway for the treatment of metabolic diseases.

Indexed as

Insulin ResistanceAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesAnimalsDiabetes Mellitus, Type 2Drug DiscoveryHumansLiverMetabolic DiseasesProtein Serine-Threonine KinasesSignal TransductionAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesProtein Serine-Threonine KinasesSTK11 protein, human

Identifiers

PMID21428801
PMCPMC4122297
OpenAlexW2068872278

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.