Evidence map›Paper›PMID 37725232›Full record

ReviewFrontiers of medicine2023

Immunometabolism: a new dimension in immunotherapy resistance.

Chaoyue Xiao, Wei Xiong, Yiting Xu, Ji'an Zou, Yue Zeng, Junqi Liu, Yurong Peng, Chunhong Hu, Fang Wu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Frontiers of medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 3 institutions in 1 country.

Chaoyue XiaoDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Wei XiongNHC Key Laboratory of Carcinogenesis and Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha, 410078, China.
Yiting XuXiangya School of Medicine, Central South University, Changsha, 410013, China.
Ji'an ZouXiangya School of Medicine, Central South University, Changsha, 410013, China.
Yue ZengDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Junqi LiuDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Yurong PengDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Chunhong HuDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Fang WuDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China. wufang4461@csu.edu.cn.
Central South University · CNHunan Cancer Hospital · CNSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) have demonstrated unparalleled clinical responses and revolutionized the paradigm of tumor treatment, while substantial patients remain unresponsive or develop resistance to ICIs as a single agent, which is traceable to cellular metabolic dysfunction. Although dysregulated metabolism has long been adjudged as a hallmark of tumor, it is now increasingly accepted that metabolic reprogramming is not exclusive to tumor cells but is also characteristic of immunocytes. Correspondingly, people used to pay more attention to the effect of tumor cell metabolism on immunocytes, but in practice immunocytes interact intimately with their own metabolic function in a way that has never been realized before during their activation and differentiation, which opens up a whole new frontier called immunometabolism. The metabolic intervention for tumor-infiltrating immunocytes could offer fresh opportunities to break the resistance and ameliorate existing ICI immunotherapy, whose crux might be to ascertain synergistic combinations of metabolic intervention with ICIs to reap synergic benefits and facilitate an adjusted anti-tumor immune response. Herein, we elaborate potential mechanisms underlying immunotherapy resistance from a novel dimension of metabolic reprogramming in diverse tumor-infiltrating immunocytes, and related metabolic intervention in the hope of offering a reference for targeting metabolic vulnerabilities to circumvent immunotherapeutic resistance.

Indexed as

NeoplasmsHumansImmune Checkpoint InhibitorsImmunotherapyImmune Checkpoint Inhibitorsimmune cellimmune checkpoint inhibitorimmunometabolismimmunotherapymetabolic reprogrammingresistancetumor microenvironment

Identifiers

PMID37725232
OpenAlexW4386864831

What Socratic holds

Textmetadata
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.