Evidence map›Paper›PMID 35477416›Full record

ReviewJournal of hematology & oncology2022

Targeting nucleotide metabolism: a promising approach to enhance cancer immunotherapy.

Huai-Liang Wu, Yue Gong, Peng Ji, Yi-Fan Xie, Yi-Zhou Jiang, Guang-Yu Liu

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
25.4field-weighted citation impact, top 1% 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

112 citing papers in PubMed, 180 citations in OpenAlex.

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52 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Huai-Liang Wu *Key Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery, Department of Oncology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Xuhui District, Shanghai, 200032, People's Republic of China.
Yue Gong *Key Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery, Department of Oncology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Xuhui District, Shanghai, 200032, People's Republic of China.
Peng JiKey Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery, Department of Oncology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Xuhui District, Shanghai, 200032, People's Republic of China.
Yi-Fan XieKey Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery, Department of Oncology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Xuhui District, Shanghai, 200032, People's Republic of China.
Yi-Zhou JiangKey Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery, Department of Oncology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Xuhui District, Shanghai, 200032, People's Republic of China. yizhoujiang@fudan.edu.cn.
Guang-Yu LiuKey Laboratory of Breast Cancer in Shanghai, Department of Breast Surgery, Department of Oncology, Fudan University Shanghai Cancer Center, 270 Dongan Road, Xuhui District, Shanghai, 200032, People's Republic of China. liugy688@163.com.ORCID 0000-0002-1752-026X
Fudan University Shanghai Cancer Center · CN

Funding

Shanghai Minhang Science and Technology Commission 19411966700
6 · The paper itself

Abstract

Targeting nucleotide metabolism can not only inhibit tumor initiation and progression but also exert serious side effects. With in-depth studies of nucleotide metabolism, our understanding of nucleotide metabolism in tumors has revealed their non-proliferative effects on immune escape, indicating the potential effectiveness of nucleotide antimetabolites for enhancing immunotherapy. A growing body of evidence now supports the concept that targeting nucleotide metabolism can increase the antitumor immune response by (1) activating host immune systems via maintaining the concentrations of several important metabolites, such as adenosine and ATP, (2) promoting immunogenicity caused by increased mutability and genomic instability by disrupting the purine and pyrimidine pool, and (3) releasing nucleoside analogs via microbes to regulate immunity. Therapeutic approaches targeting nucleotide metabolism combined with immunotherapy have achieved exciting success in preclinical animal models. Here, we review how dysregulated nucleotide metabolism can promote tumor growth and interact with the host immune system, and we provide future insights into targeting nucleotide metabolism for immunotherapeutic treatment of various malignancies.

Indexed as

ImmunotherapyNeoplasmsAnimalsHumansImmunologic FactorsNucleotidesImmunologic FactorsNucleotides

Identifiers

PMID35477416
PMCPMC9044757
OpenAlexW4224940474

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.