Evidence map›Paper›PMID 36558071›Full record

ReviewMolecules (Basel, Switzerland)2022

Comparative G-Protein-Coupled Estrogen Receptor (GPER) Systems in Diabetic and Cancer Conditions: A Review.

Aliyu Muhammad, Gilead Ebiegberi Forcados, Abdurrahman Pharmacy Yusuf, Murtala Bello Abubakar, Idris Zubairu Sadiq, Isra Elhussin, Md Abu Talha Siddique, Suleiman Aminu, Rabiatu Bako Suleiman, Yakubu Saddeeq Abubakar and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Prostate Cancer and the Mevalonate Pathway.International journal of molecular sciences · 2024
    Review
  7. Review
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

13 authors at 5 institutions in 2 countries.

Aliyu MuhammadCenter for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.ORCID 0000-0002-4167-7793
Gilead Ebiegberi ForcadosBiochemistry Division, National Veterinary Research Institute, Vom P.M.B. 01, Nigeria.
Abdurrahman Pharmacy YusufDepartment of Biochemistry, School of Life Sciences, Federal University of Technology, Minna P.M.B. 65, Nigeria.ORCID 0000-0003-0404-5233
Murtala Bello AbubakarDepartment of Physiology, Faculty of Basic Medical Sciences, College of Health Sciences, Usmanu Danfodiyo University, Sokoto P.M.B. 2254, Nigeria.ORCID 0000-0001-7666-4776
Idris Zubairu SadiqDepartment of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
Isra ElhussinCenter for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.
Md Abu Talha SiddiqueCenter for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.
Suleiman AminuDepartment of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.ORCID 0000-0002-6520-8596
Rabiatu Bako SuleimanDepartment of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
Yakubu Saddeeq AbubakarDepartment of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.ORCID 0000-0002-5228-0548
Babangida Sanusi KatsayalDepartment of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.ORCID 0000-0002-7518-281X
Clayton C YatesCenter for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.ORCID 0000-0001-5420-9852
Sunila MahavadiCenter for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.
Ahmadu Bello University · NGCenter for Cancer Research · USFederal University of Technology Minna · NGNational Veterinary Research Institute · NGUsmanu Danfodiyo University · NG

Funding

Tuskegee University Center for Biomedical Research/ Research Centers at Minority InstitutionsU54MD007585 · NIMHD · TUSKEGEE UNIVERSITY · PI Balasubramanyam Karanam · 2017 to 2026
$29.4M
Research Education CoreU54CA118623 · NCI · TUSKEGEE UNIVERSITY · PI Vivian L Carter, TIMOTHY TURNER · 2005 to 2026
$20.2M
Gender Bias in Gastrointestinal Motility in Health and DiabetesR01DK124269 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI MAHAVADI, SUNILA · 2021 to 2025
$1.9M
NCI NIH HHS U54 CA118623NIDDK NIH HHS R01 DK124269NIH HHS DK124269NIMHD NIH HHS U54 MD007585NIMHD NIH HHS U54-MD007585-26
6 · The paper itself

Abstract

For many patients, diabetes Mellitus and Malignancy are frequently encountered comorbidities. Diabetes affects approximately 10.5% of the global population, while malignancy accounts for 29.4 million cases each year. These troubling statistics indicate that current treatment approaches for these diseases are insufficient. Alternative therapeutic strategies that consider unique signaling pathways in diabetic and malignancy patients could provide improved therapeutic outcomes. The G-protein-coupled estrogen receptor (GPER) is receiving attention for its role in disease pathogenesis and treatment outcomes. This review aims to critically examine GPER' s comparative role in diabetes mellitus and malignancy, identify research gaps that need to be filled, and highlight GPER's potential as a therapeutic target for diabetes and malignancy management. There is a scarcity of data on GPER expression patterns in diabetic models; however, for diabetes mellitus, altered expression of transport and signaling proteins has been linked to GPER signaling. In contrast, GPER expression in various malignancy types appears to be complex and debatable at the moment. Current data show inconclusive patterns of GPER expression in various malignancies, with some indicating upregulation and others demonstrating downregulation. Further research should be conducted to investigate GPER expression patterns and their relationship with signaling pathways in diabetes mellitus and various malignancies. We conclude that GPER has therapeutic potential for chronic diseases such as diabetes mellitus and malignancy.

Indexed as

Diabetes MellitusNeoplasmsEstrogensGTP-Binding ProteinsHumansReceptors, EstrogenReceptors, G-Protein-CoupledSignal TransductionEstrogensGTP-Binding ProteinsReceptors, EstrogenReceptors, G-Protein-Coupledbiosignalingdiabetes mellitusG-protein-coupled estrogen receptormalignancytherapeutics

Identifiers

PMID36558071
PMCPMC9786783
OpenAlexW4312211546

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.