Evidence map›Paper›PMID 25614086›Full record

ArticleInternational journal of obesity (2005)2015

Transcription factor TIP27 regulates glucose homeostasis and insulin sensitivity in a PI3-kinase/Akt-dependent manner in mice.

L Yuan, X Luo, M Zeng, Y Zhang, M Yang, L Zhang, R Liu, G Boden, H Liu, Z A Ma and 2 more

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Article in International journal of obesity (2005), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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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

12 authors at 6 institutions in 3 countries.

L YuanDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
X LuoKey Laboratory of Diagnostic Medicine (Ministry of Education) and Department of Clinical Biochemistry, College of Laboratory Medicine, Chongqing Medical University, Chongqing, China.
M ZengDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
Y ZhangDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
M Yang1] Department of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China [2] Translational Research Institute, Brisbane, QLD, Australia.
L ZhangDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
R LiuDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
G BodenThe Division of Endocrinology/Diabetes/Metabolism and the Clinical Research Center, Temple University School of Medicine, Philadelphia, PA, USA.
H LiuDepartment of Pediatrics, University of Mississippi Medical Center, Mississippi, MS, USA.
Z A MaTechnology Transfer Center, University of Michigan, Ann Arbor, MI, USA.
L LiDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
G YangDepartment of Endocrinology, Second Affiliated Hospital Chongqing Medical University, Chongqing, China.
Dalian Medical University · CNChongqing Medical University · CNUniversity of Mississippi Medical Center · USSecond Affiliated Hospital of Chongqing Medical University · CNTemple University · USUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesJuxtaposed with another zinc-finger gene 1 (TIP27 or JAZF1) is a 27-kDa transcription factor, and genome-wide association studies have recently revealed TIP27 to be associated with type 2 diabetes. However, little is known about its role in the regulation of metabolism. In this study, we investigated the effects of TIP27 overexpression on glucose homeostasis and insulin signaling in high-fat diet (HFD)-fed TIP27 transgenic (TIP27-Tg) mice and db/db mice.

methodsWe assessed the effects of TIP27 overexpression in both TIP27-Tg mice and db/db mice on glucose metabolism and changes in insulin sensitivity during glucose (GTT) and insulin (ITT) tolerance tests. A hyperinsulinemic-euglycemic clamp was performed on TIP27-Tg mice. Real-time quantitative PCR and western blotting were used to assess mRNA and protein expressions.

resultsTIP27 overexpression in TIP27-Tg mice and in db/db mice led to reduced total cholesterol and fasting plasma insulin levels, and enhanced glucose tolerance and insulin sensitivity during GTT and ITT. Hyperinsulinemic-euglycemic clamp experiments demonstrated that HFD-fed TIP27-Tg mice had lower hepatic glucose production and higher insulin sensitivity compared with nontransgenic littermates. In addition, the hepatic expressions of phosphoenolpyruate carboxykinase (PEPCK), glucose-6-phosphatase (G6Pase) mRNAs and proteins were significantly decreased, whereas the phosphorylation of insulin receptor, insulin receptor substrate-1, adenosine monophosphate-activated protein kinase and Akt kinase (Akt) in the liver was significantly increased in HFD-fed TIP27-Tg mice compared with nontransgenic littermates. Adenovirus-mediated TIP27 overexpression in db/db mice also decreased the expression of gluconeogenic genes and increased the phosphorylation of insulin signaling molecules in the liver compared with controls. Finally, LY294002, a phosphatidylinositol 3-kinase (PI3-kinase) inhibitor, abolished the suppressive effect of TIP27 overexpression on PEPCK and G6Pase expression.

conclusionsTIP27 has an important role in glucose homeostasis through the regulation of hepatic glucose metabolism and insulin sensitivity. Furthermore, this regulation requires activation of PI3-kinase.

Indexed as

Insulin ResistanceAnimalsBlood GlucoseGenome-Wide Association StudyGlucose Clamp TechniqueMaleMiceMice, Inbred C57BLMice, TransgenicNeoplasm ProteinsPhosphatidylinositol 3-KinasePhosphorylationPromoter Regions, GeneticSignal TransductionTranscription FactorsBlood GlucoseNeoplasm ProteinsPhosphatidylinositol 3-KinaseTranscription Factors

Identifiers

PMID25614086
OpenAlexW2030725376

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.