Evidence map›Paper›PMID 36411477›Full record

ArticleEuropean journal of medical research2022

Tumor microenvironment-associated lactate metabolism regulates the prognosis and precise checkpoint immunotherapy outcomes of patients with lung adenocarcinoma.

Song Qiu, Ying Wang, Hui Rao, Qiuyang Que, Yanyang Wu, Rui Zhu, Xiaofei Feng, Jun Chi, Weiling Lai, Yihang Sun and 3 more

Open access · goldAbstract read
In one paragraph

Article in European journal of medical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
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

13 authors at 3 institutions in 1 country.

Song Qiu *Department of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Ying Wang *Department of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Hui Rao *Department of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Qiuyang QueDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Yanyang WuDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Rui ZhuDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Xiaofei FengDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Jun ChiDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Weiling LaiDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China.
Yihang SunSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Qi XiaoJiangkou Town Central Health Center, Ganxian District, Ganzhou, China.
Huaqiu ShiDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China. shq3677274@163.com.
Yi XiangDepartment of Oncology, The First Affiliated Hospital, Gannan Medical University, No 23, Qingnian Road, Ganzhou, China. xiangyi_xiangyi@126.com.
First Affiliated Hospital of Gannan Medical University · CNGanzhou People's Hospital · CNSouthern Medical University · CN

Funding

Scientific Research Foundation of Gannan Medical University 2021DQ095
6 · The paper itself

Abstract

backgroundDespite the wide clinical application of checkpoint inhibitor immunotherapy in lung adenocarcinoma, its limited benefit to patients remains puzzling to researchers. One of the mechanisms of immunotherapy resistance may be the dysregulation of lactate metabolism in the immunosuppressive tumor microenvironment (TME), which can inhibit dendritic cell maturation and prevent T-cell invasion into tumors. However, the key genes related to lactate metabolism and their influence on the immunotherapeutic effects in lung adenocarcinoma have not yet been investigated in depth.

methodsIn this study, we first surveyed the dysregulated expression of genes related to lactate metabolism in lung adenocarcinoma and then characterized their biological functions. Using machine learning methods, we constructed a lactate-associated gene signature in The Cancer Genome Atlas cohort and validated its effectiveness in predicting the prognosis and immunotherapy outcomes of patients in the Gene Expression Omnibus cohorts.

resultsA 7-gene signature based on the metabolomics related to lactate metabolism was found to be associated with multiple important clinical features of cancer and was an independent prognostic factor.

conclusionsThese results suggest that rather than being simply a metabolic byproduct of glycolysis, lactate in the TME can affect immunotherapy outcomes. Therefore, the mechanism underlying this effect of lactate is worthy of further study.

Indexed as

Adenocarcinoma of LungLung NeoplasmsHumansImmunotherapyLactatesPrognosisTumor MicroenvironmentLactatesGene signatureImmunotherapy benefitLactate metabolismLung adenocarcinomaPrognosisRisk score

Identifiers

PMID36411477
PMCPMC9677690
OpenAlexW4309661150

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.