Evidence map›Paper›PMID 35179267›Full record

ArticleCell proliferation2022

Dynamic changes of exhaustion features in T cells during oral carcinogenesis.

Wenqiang Xie, Jie Shen, Dikan Wang, Junyi Guo, Qunxing Li, Shuqiong Wen, Wenxiao Dai, Liling Wen, Huanzi Lu, Juan Fang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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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

11 authors at 3 institutions in 1 country.

Wenqiang XieGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Jie ShenSchool of Stomatology, Zhejiang University School of Medicine, Clinical Research Center for Oral Disease of Zhejiang Province, Key Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Hangzhou, PR China.
Dikan WangGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Junyi GuoGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Qunxing LiDepartment of Stomatology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, PR China.
Shuqiong WenGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Wenxiao DaiGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Liling WenGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Huanzi LuGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Juan FangGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.
Zhi WangGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology, Stomatological Hospital, Sun Yat-Sen University, Guangzhou, PR China.ORCID https://orcid.org/0000-0002-5276-1413
Guangdong Province Stomatological Hospital · CNSun Yat-sen University · CNZhejiang University · CN

Funding

Guangdong Basic and Applied Basic Research Foundation 2020A1515110741National Natural Science Foundation of China 81772896National Natural Science Foundation of China 81972532National Natural Science Foundation of China 82101017
6 · The paper itself

Abstract

objectivesThis study aimed to clarify the dynamic changes of exhaustion features in T cells during oral carcinogenesis. MATERIALS AND

methodsMice were randomly divided into 4NQO group and control group. The exhaustion features of CD4

resultsThe proportion of naive T cells in 4NQO group was lower than those in control group, while the proportion of effector memory T cells was higher in 4NQO group. The expression of inhibitory receptors on CD4

conclusionsT-cell dysfunction was established at the early premalignant phase of oral carcinogenesis; PD-1 blockade at the early premalignant phase can effectively reverse T-cell exhaustion features and then prevent carcinogenesis progression.

Indexed as

CD8-Positive T-LymphocytesProgrammed Cell Death 1 ReceptorAnimalsCarcinogenesisMiceProgrammed Cell Death 1 Receptorcytokine secretioninhibitory receptorsoral carcinogenesisPD-1 blockaderegulatory T cell (Treg)T cell exhaustion

Identifiers

PMID35179267
PMCPMC9055910
OpenAlexW4213369432

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.