Evidence map›Paper›PMID 42344927›Full record

ReviewFrontiers in immunology2026

Mitochondria: from powerhouses of cells to hubs in antitumor immunity.

Xiaofeng Li, Yanfeng Shi, Yan Zhao, Gengjun Zhu, Lifang Jin

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. 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

5 authors.

Xiaofeng LiDepartment of Oncology and Hematology, The Second Hospital of Jilin University, Changchun, China.
Yanfeng ShiMedical Records Department, The Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, China.
Yan ZhaoDepartment of Oncology and Hematology, The Second Hospital of Jilin University, Changchun, China.
Gengjun ZhuDepartment of Oncology and Hematology, The Second Hospital of Jilin University, Changchun, China.
Lifang JinDepartment of Oncology and Hematology, The Second Hospital of Jilin University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While immune checkpoint inhibitors and chimeric antigen receptor T-cell (CAR-T) therapies constitute the cornerstone of current immunotherapy, their efficacy is often limited by, most notably, the immunosuppressive tumor microenvironment. Recently, mitochondria are recognized as pivotal metabolic-immune hubs that critically support tumor progression, metastasis, and immune evasion. However, this insight has not yet translated into a clear understanding of the underlying mechanisms or their therapeutic potential. This review summarizes the role of mitochondria in cellular metabolic regulation, with a focus on mitochondrial-mediated metabolic reprogramming in cancer and immune cells within the tumor microenvironment. We then discuss therapeutic opportunities to potentiate antitumor immunity by targeting mitochondrial reprogramming in cancer and CAR-T cells. Finally, we offer a forward-looking perspective on emerging mitochondria-targeted strategies, such as mitochondrial vaccines, precise mtDNA editing, and engineered mitochondrial transplantation.

Indexed as

MitochondriaNeoplasmsAnimalsHumansImmunotherapy, AdoptiveMetabolic ReprogrammingReceptors, Chimeric AntigenTumor MicroenvironmentReceptors, Chimeric Antigenantitumor immunityCAR-Tmetabolic reprogrammingmitochondriatumor microenvironment

Identifiers

PMID42344927
PMCPMC13286946

What Socratic 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 Socratic graph.