Evidence map›Paper›PMID 40046060›Full record

ReviewFrontiers in immunology2025

Na+/K+-ATPase: a multifunctional target in type 2 diabetes and pancreatic islets.

Lisha Mou, Zhenkun Fu, Tony Bowei Wang, Yuxian Chen, Ziqi Luo, Xinyu Wang, Zuhui Pu

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Lisha MouDepartment of Endocrinology, Institute of Translational Medicine, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Guangxi University of Chinese Medicine, Shenzhen, Guangdong, China.
Zhenkun FuDepartment of Endocrinology, Institute of Translational Medicine, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Guangxi University of Chinese Medicine, Shenzhen, Guangdong, China.
Tony Bowei WangBiology Department, Skidmore College, Saratoga Springs, NY, United States.
Yuxian ChenDepartment of Endocrinology, Institute of Translational Medicine, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Guangxi University of Chinese Medicine, Shenzhen, Guangdong, China.
Ziqi LuoDepartment of Endocrinology, Institute of Translational Medicine, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Guangxi University of Chinese Medicine, Shenzhen, Guangdong, China.
Xinyu WangDepartment of Endocrinology, Institute of Translational Medicine, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Guangxi University of Chinese Medicine, Shenzhen, Guangdong, China.
Zuhui PuMetaLife Lab, Shenzhen Institute of Translational Medicine, Shenzhen, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes (T2D) is a widespread metabolic disorder marked by hyperglycemia, arising from insulin resistance and relative insulin deficiency. This review investigates the critical role of Na+/K+-ATPase (NKA), a transmembrane protein essential for maintaining cellular ion gradients, in the pathophysiology of T2D. We provide an overview of NKA's biological functions, emphasizing its involvement in cellular signaling pathways, insulin secretion, and glucose homeostasis. The potential of NKA as a therapeutic target for T2D is analyzed, showcasing innovative strategies such as NKA activators, gene therapy, and stem cell therapy aimed at enhancing NKA activity to achieve better glycemic control. Additionally, NKA's multifunctional role in maintaining cell viability and modulating immune responses in islet transplantation may offer potential benefits for improving transplant outcomes. By elucidating the complex interactions between NKA and T2D, this review aims to shed light on developing novel therapeutic interventions that meet the multifaceted needs of individuals suffering from this chronic condition, ultimately improving their health outcomes.

Indexed as

Diabetes Mellitus, Type 2Islets of LangerhansSodium-Potassium-Exchanging ATPaseAnimalsHumansSignal TransductionSodium-Potassium-Exchanging ATPasediabetesgene therapyisletsodium-potassium ATPasestem cell therapytherapeutic targettype 2 diabetesβ-cells

Identifiers

PMID40046060
PMCPMC11880247

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Registered trials

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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.