Evidence map›Paper›PMID 32940722›Full record

ReviewCellular and molecular life sciences : CMLS2021

Immune landscape and therapeutic strategies: new insights into PD-L1 in tumors.

Yuan Wei, Xiao Xiao, Xiang-Ming Lao, Limin Zheng, Dong-Ming Kuang

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2021. 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. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
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

5 authors.

Yuan WeiThe Fifth Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Xiao XiaoCancer Program, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Xiang-Ming LaoState Key Laboratory of Oncology in Southern China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University, Guangzhou, China. laoxm@sysucc.org.cn.
Limin ZhengState Key Laboratory of Oncology in Southern China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University, Guangzhou, China. zhenglm@mail.sysu.edu.cn.
Dong-Ming KuangThe Fifth Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China. kdming@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0003-3570-9717

Funding

China Postdoctoral Science Foundation 2019M653191Fundamental Research Funds for the Central Universities 19lgjc09Fundamental Research Funds for the Central Universities 19lgpy167National Key Research and Development Plan of China 2016YFA0502600National Key Research and Development Plan of China 2018ZX10302205National Natural Science Foundation of China 31830025National Natural Science Foundation of China 81901585Natural Science Foundation of Guangdong Province, China 2018B030308010Natural Science Foundation of Guangdong Province, China 2019A1515011770
6 · The paper itself

Abstract

PD-1/PD-L1 axis represents an important target for renormalizing and resetting anti-tumor immunity in cancer patients. Currently, anti-PD-1/PD-L1 therapy has been applied in a broad spectrum of tumors and has yielded durable remission in patients. However, how to further broaden the application, guide personalized therapeutic strategies, and improve clinical responses remains a vital task. At present, PD-L1 expression is an important parameter of clinical indications for immune checkpoint blockade in many types of cancers, a strategy based on the supposition that positive PD-L1 expression reflects local T cell response. Recent studies have revealed that PD-L1 expression is regulated by multiple layers of complicated factors, during which the host immune microenvironment exerts a pivotal role and determines the clinical efficacy of the therapy. In this review, we will summarize recent findings on PD-1/PD-L1 in cancer, focusing on how local immune landscape participates in the regulation of PD-L1 expression and modification. Importantly, we will also discuss these topics in the context of clinical treatment and analyze how these fundamental principles might inspire our efforts to develop more precise and effective immune therapeutics for cancer.

Indexed as

Antibodies, MonoclonalB7-H1 AntigenHumansImmune Checkpoint InhibitorsNeoplasmsProgrammed Cell Death 1 ReceptorProtein Processing, Post-TranslationalSignal TransductionT-LymphocytesTumor MicroenvironmentAntibodies, MonoclonalB7-H1 AntigenImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorCombinatorial immune checkpoint therapyEpigenetic reprogrammingExosomal PD-L1Immune microenvironmentMetabolic reprogrammingPD-L1 expression

Identifiers

PMID32940722
PMCPMC11072479

What OpenQuestion holds

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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.