Evidence map›Paper›PMID 27516169›Full record

ReviewNature reviews. Drug discovery2016

Targeting hepatic glucose metabolism in the treatment of type 2 diabetes.

Amy K Rines, Kfir Sharabi, Clint D J Tavares, Pere Puigserver

Abstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed
15.1field-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

152 citing papers in PubMed, 373 citations in OpenAlex.

  1. Trial
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  4. Liver-Specific Suppression of PLA2G6/iPLAFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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  18. Observational
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92 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 2 institutions in 1 country.

Amy K RinesDepartment of Cancer Biology, Dana-Farber Cancer Institute, and Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Kfir SharabiDepartment of Cancer Biology, Dana-Farber Cancer Institute, and Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Clint D J TavaresDepartment of Cancer Biology, Dana-Farber Cancer Institute, and Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Pere PuigserverDepartment of Cancer Biology, Dana-Farber Cancer Institute, and Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Dana-Farber Cancer Institute · USHarvard University · US

Funding

Chemical Biology of Mitochondria and DiabetesR24DK080261 · NIDDK · DANA-FARBER CANCER INST · PI SPIEGELMAN, BRUCE M. · 2007 to 2016
$13.9M
Transcriptional Control of Mitochondrial Bioenergetic FunctionR01DK081418 · NIDDK · DANA-FARBER CANCER INST · PI PUIGSERVER, PERE · 2008 to 2021
$5.2M
Control of Nutrient Homeostasis through PGC-1alpha and SIRT1R01DK069966 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PUIGSERVER, PERE · 2005 to 2014
$4.2M
Insulin Signaling and Metabolic Effects through CLK2 KinaseR01DK089883 · NIDDK · DANA-FARBER CANCER INST · PI PUIGSERVER, PERE · 2011 to 2020
$3.8M
Mechanisms of brown and beige fat stimulation by a PGC-1a-activating compoundF32DK102293 · NIDDK · DANA-FARBER CANCER INST · PI RINES, AMY KATHERINE · 2014 to 2016
$152k
NIDDK NIH HHS F32 DK102293NIDDK NIH HHS R01 DK069966NIDDK NIH HHS R01 DK081418NIDDK NIH HHS R01 DK089883NIDDK NIH HHS R24 DK080261
6 · The paper itself

Abstract

Type 2 diabetes mellitus is characterized by the dysregulation of glucose homeostasis, resulting in hyperglycaemia. Although current diabetes treatments have exhibited some success in lowering blood glucose levels, their effect is not always sustained and their use may be associated with undesirable side effects, such as hypoglycaemia. Novel antidiabetic drugs, which may be used in combination with existing therapies, are therefore needed. The potential of specifically targeting the liver to normalize blood glucose levels has not been fully exploited. Here, we review the molecular mechanisms controlling hepatic gluconeogenesis and glycogen storage, and assess the prospect of therapeutically targeting associated pathways to treat type 2 diabetes.

Indexed as

AnimalsDiabetes Mellitus, Type 2Drug Delivery SystemsGlucoseHumansHypoglycemic AgentsLiverSignal TransductionGlucoseHypoglycemic Agents

Identifiers

PMID27516169
PMCPMC5751421
OpenAlexW2509220708

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.