Evidence map›Paper›PMID 42113690›Full record

ReviewChannels (Austin, Tex.)2026

Transient receptor potential canonical (TRPC) channels in diabetes and associated complications.

Yi Wu, Shengming Chen, Xiaolu Xia

Abstract readReview
In one paragraph

Review in Channels (Austin, Tex.), 2026. 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

3 authors.

Yi WuCollaborative Innovation Center for Biomedicine, Shanghai University of Medicine and Health Sciences, Shanghai, China.ORCID 0000-0002-3138-2844
Shengming ChenSchool of Pharmacy, Shanghai University of Medicine and Health Sciences, Shanghai, China.
Xiaolu XiaSchool of Pharmacy, Shanghai University of Medicine and Health Sciences, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TRPC channels are widely expressed in various tissues and cell types, and accumulating evidence indicates that they play critical roles in pancreatic β cell function, including the regulation of insulin secretion. Moreover, TRPC channels have been implicated in the pathogenesis of type 2 diabetes mellitus (T2DM) and its associated complications, underscoring their potential as therapeutic targets. Despite this, there remains a lack of comprehensive, up-to-date reviews summarizing the distribution and functional roles of TRPC channels in diabetes and its complications. In addition, the expression patterns and physiological significance of certain TRPC subtypes remain controversial. This review, therefore, aims to provide a thorough overview of current research, starting with general aspects of TRPC channel structure and function, and progressing to their physiological and pathological roles, with particular emphasis on their involvement in insulin secretion, insulin resistance, diabetes, and diabetic complications.

Indexed as

Diabetes ComplicationsDiabetes Mellitus, Type 2TRPC Cation ChannelsAnimalsHumansInsulinInsulin ResistanceInsulin-Secreting CellsInsulin SecretionInsulinTRPC Cation Channelsdiabetesdiabetic complicationsinsulin resistanceinsulin secretionTRPC channels

Identifiers

PMID42113690
PMCPMC13166186

What OpenQuestion holds

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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.