Evidence map›Paper›PMID 33159034›Full record

ReviewCell death & disease2020

PD-L1 degradation pathway and immunotherapy for cancer.

Qian Gou, Chen Dong, Huihui Xu, Bibimaryam Khan, Jianhua Jin, Qian Liu, Juanjuan Shi, Yongzhong Hou

Open access · goldAbstract readReview
In one paragraph

Review in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 188 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
188citing papers in PubMed, 3 pooled it
9.2field-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

188 citing papers in PubMed, 3 syntheses or guidelines pooled it, 294 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Programmed Cell Death Protein 1-Interleukin-2 Bispecific Agents for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  18. Granzyme B PET/CT predicts chemo-immunotherapy outcomes in microsatellite stable gastric cancers.European journal of nuclear medicine and molecular imaging · 2026
    Article
  19. Review
  20. Review

128 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

8 authors at 1 institution in 1 country.

Qian GouDepartment of Oncology, The Affiliated Wujin Hospital, Jiangsu University, Changzhou, Jiangsu Province, 213017, China.
Chen DongSchool of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu Province, 212013, China.
Huihui XuSchool of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu Province, 212013, China.
Bibimaryam KhanSchool of Medicine, Jiangsu University, Zhenjiang, Jiangsu Province, 212013, China.
Jianhua JinDepartment of Oncology, The Affiliated Wujin Hospital, Jiangsu University, Changzhou, Jiangsu Province, 213017, China.
Qian LiuDepartment of Oncology, The Affiliated Wujin Hospital, Jiangsu University, Changzhou, Jiangsu Province, 213017, China.
Juanjuan ShiSchool of Medicine, Jiangsu University, Zhenjiang, Jiangsu Province, 212013, China.
Yongzhong HouDepartment of Oncology, The Affiliated Wujin Hospital, Jiangsu University, Changzhou, Jiangsu Province, 213017, China. houyz@ujs.edu.cn.ORCID 0000-0003-2019-8686
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed death ligand 1 (PD-L1, CD274) is an essential immune checkpoint protein that binds to programmed death 1 (PD-1) on T-lymphocytes. T cell plays a critical role in killing cancer cells while the cancer cell exhibits immune escape by the expression of PD-L1. The binding of PD-L1 to PD-1 inhibits T cell proliferation and activity, leading to tumor immunosuppression. Increasing evidence shows that PD-L1 protein undergoes degradation in proteasomes or lysosomes by multiple pathways, leading to enhanced immunotherapy for cancer. Although some specific drugs induce PD-L1 degradation and increase antitumor activity, the combination of these drugs with PD-L1/PD-1 blockade significantly enhances cancer immunotherapy. In this review, we have discussed the interaction of PD-L1 degradation with cancer immunotherapy.

Indexed as

ProteolysisAnimalsB7-H1 AntigenHumansImmunotherapyNeoplasmsB7-H1 AntigenCD274 protein, human

Identifiers

PMID33159034
PMCPMC7648632
OpenAlexW3095431398

What OpenQuestion 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 OpenQuestion graph.