Evidence map›Paper›PMID 38068822›Full record

ReviewNutrients2023

The Role of Cdc42 in the Insulin and Leptin Pathways Contributing to the Development of Age-Related Obesity.

Bauyrzhan Umbayev, Timur Saliev, Yuliya Safarova Yantsen, Aislu Yermekova, Farkhad Olzhayev, Denis Bulanin, Andrey Tsoy, Sholpan Askarova

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Bauyrzhan UmbayevNational Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0000-0002-0286-7252
Timur SalievS.D. Asfendiyarov Kazakh National Medical University, Almaty 050012, Kazakhstan.ORCID 0000-0001-5696-6363
Yuliya Safarova YantsenNational Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0000-0003-0695-0413
Aislu YermekovaNational Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0009-0004-2586-9770
Farkhad OlzhayevNational Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0000-0002-1906-6654
Denis BulaninDepartment of Biomedical Sciences, School of Medicine, Nazarbayev University, Astana 010000, Kazakhstan.
Andrey TsoyNational Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0000-0003-3818-3079
Sholpan AskarovaNational Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0000-0001-6161-1671
Nazarbayev University · KZKazakh National Medical University · KZ

Funding

CSRD VA 1
6 · The paper itself

Abstract

Age-related obesity significantly increases the risk of chronic diseases such as type 2 diabetes, cardiovascular diseases, hypertension, and certain cancers. The insulin-leptin axis is crucial in understanding metabolic disturbances associated with age-related obesity. Rho GTPase Cdc42 is a member of the Rho family of GTPases that participates in many cellular processes including, but not limited to, regulation of actin cytoskeleton, vesicle trafficking, cell polarity, morphology, proliferation, motility, and migration. Cdc42 functions as an integral part of regulating insulin secretion and aging. Some novel roles for Cdc42 have also been recently identified in maintaining glucose metabolism, where Cdc42 is involved in controlling blood glucose levels in metabolically active tissues, including skeletal muscle, adipose tissue, pancreas, etc., which puts this protein in line with other critical regulators of glucose metabolism. Importantly, Cdc42 plays a vital role in cellular processes associated with the insulin and leptin signaling pathways, which are integral elements involved in obesity development if misregulated. Additionally, a change in Cdc42 activity may affect senescence, thus contributing to disorders associated with aging. This review explores the complex relationships among age-associated obesity, the insulin-leptin axis, and the Cdc42 signaling pathway. This article sheds light on the vast molecular web that supports metabolic dysregulation in aging people. In addition, it also discusses the potential therapeutic implications of the Cdc42 pathway to mitigate obesity since some new data suggest that inhibition of Cdc42 using antidiabetic drugs or antioxidants may promote weight loss in overweight or obese patients.

Indexed as

Diabetes Mellitus, Type 2InsulinGlucoseHumansLeptinObesityGlucoseInsulinLeptinage-related obesityagingCdc42insulin–leptin axisinsulin resistanceleptin resistance

Identifiers

PMID38068822
PMCPMC10707920
OpenAlexW4389131804

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.