Evidence map›Paper›PMID 38816578›Full record

ArticleCell death and differentiation2024

PD-L2 drives resistance to EGFR-TKIs: dynamic changes of the tumor immune environment and targeted therapy.

Simeng Wang, Dongliang Su, Han Chen, Jia-Cheng Lai, Chengfang Tang, Yu Li, Yidong Wang, Yuan Yang, Mingze Qin, Lina Jia and 4 more

Abstract read
In one paragraph

Article in Cell death and differentiation, 2024. 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
–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

6 citing papers in PubMed.

  1. Article
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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

14 authors.

Simeng WangDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Dongliang SuDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Han ChenDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Jia-Cheng LaiDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Chengfang TangDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Yu LiDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Yidong WangDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Yuan YangDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Mingze QinKey Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Lina JiaDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Wei CuiDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Jingyu YangDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China.
Lihui Wang *Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China. lhwang@syphu.edu.cn.
Chunfu Wu *Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang, 110016, PR China. wucf@syphu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a lack of effective treatments to overcome resistance to EGFR-TKIs in EGFR mutant tumors. A deeper understanding of resistance mechanisms can provide insights into reducing or eliminating resistance, and can potentially deliver targeted treatment measures to overcome resistance. Here, we identified that the dynamic changes of the tumor immune environment were important extrinsic factors driving tumor resistance to EGFR-TKIs in EGFR mutant cell lines and syngeneic tumor-bearing mice. Our results demonstrate that the acquired resistance to EGFR-TKIs is accompanied by aberrant expression of PD-L2, leading a dynamic shift from an initially favorable tumor immune environment to an immunosuppressive phenotype. PD-L2 expression significantly affected EGFR mutant cell apoptosis that depended on the proportion and function of CD8

Indexed as

Drug Resistance, NeoplasmProgrammed Cell Death 1 Ligand 2 ProteinTumor MicroenvironmentAnimalsApoptosisCD8-Positive T-LymphocytesCell Line, TumorErbB ReceptorsFemaleHumansMiceMolecular Targeted TherapyProtein Kinase InhibitorsEGFR protein, humanErbB ReceptorsPDCD1LG2 protein, humanProgrammed Cell Death 1 Ligand 2 ProteinProtein Kinase Inhibitors

Identifiers

PMID38816578
PMCPMC11369230

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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.