Evidence map›Paper›PMID 41425581›Full record

ReviewFrontiers in immunology2025

Solute carrier protein family: physiological functions, disease associations, and therapeutic potential in immune-related disorders.

Peiyan Li, Chen Liu, Yewei Niu, Peitao Wu, Lixuan Liu, Jiamin Jin, Jinfeng Yang

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Peiyan LiDepartment of Immunology, Guilin Medical University, Guilin, China.
Chen LiuDepartment of Immunology, Guilin Medical University, Guilin, China.
Yewei NiuDepartment of Immunology, Guilin Medical University, Guilin, China.
Peitao WuDepartment of Immunology, Guilin Medical University, Guilin, China.
Lixuan LiuDepartment of Immunology, Guilin Medical University, Guilin, China.
Jiamin JinDepartment of Immunology, Guilin Medical University, Guilin, China.
Jinfeng YangDepartment of Immunology, Guilin Medical University, Guilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Solute Carrier Protein Family (SLC) is responsible for the uptake and transport of a variety of substances across the cell membrane. It plays a central role in maintaining the stability of the intracellular environment through participation in metabolic processes and the transport of drugs and toxins. The highly tissue-specific expression of SLC proteins endows them with potential applications in disease treatment and drug development. Transplant immune reactions are a major challenge in the field of organ transplantation, as graft rejection is a key factor determining the success of transplantation and long-term organ survival. SLC proteins are increasingly drawing attention for their roles in modulating immune responses, influencing transplant immune tolerance, and controlling graft rejection. By regulating the metabolism and function of immune cells, SLC proteins affect the formation and tolerance of transplant immune responses. Among them, 7 SLC proteins are "validated targets" with approved or phase III drugs, 9 are "candidate targets" in active clinical trials, and 14 remain "potential targets" supported by genetic and pre-clinical evidence. This article elucidates the functions of SLC proteins in transplant immunology, inflammation and autoimmune diseases, tumor immunology, metabolic diseases, and neurological diseases, as well as the new targets and strategies for treating these diseases that SLC proteins provide.

Indexed as

Immune System DiseasesSolute Carrier ProteinsAnimalsGraft RejectionHumansNeoplasmsOrgan TransplantationTransplantation ImmunologySolute Carrier Proteinscell metabolismimmune responsesolute carriertransplantation immunitytransplant rejection

Identifiers

PMID41425581
PMCPMC12715013

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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.