Evidence map›Paper›PMID 30680705›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2019

Nuclear localization of PD-L1: artifact or reality?

Hara Polioudaki, Amanda Chantziou, Konstantina Kalyvianaki, Panagiotis Malamos, George Notas, Dimitris Mavroudis, Marilena Kampa, Elias Castanas, Panayiotis A Theodoropoulos

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Intracellular PD-L1: Functions, Regulation, and Therapeutic Implications.International journal of biological sciences · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Prevalence of CD8Cellular oncology (Dordrecht, Netherlands) · 2020
    Article
  14. Esophageal carcinoma: Towards targeted therapies.Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  15. 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

9 authors at 1 institution in 1 country.

Hara PolioudakiDepartment of Biochemistry, School of Medicine, University of Crete, Voutes, 71013, Heraklion, Crete, Greece.
Amanda ChantziouDepartment of Biochemistry, School of Medicine, University of Crete, Voutes, 71013, Heraklion, Crete, Greece.
Konstantina KalyvianakiLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Panagiotis MalamosLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
George NotasLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Dimitris MavroudisDepartment of Medical Oncology, University General Hospital of Heraklion, Heraklion, Crete, Greece.
Marilena KampaLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Elias CastanasLaboratory of Experimental Endocrinology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Panayiotis A TheodoropoulosDepartment of Biochemistry, School of Medicine, University of Crete, Voutes, 71013, Heraklion, Crete, Greece. takis@uoc.gr.
University of Crete · GR

Funding

Special Account for Research Funds of the University of Crete KA4969
6 · The paper itself

Abstract

backgroundThe levels of expression and membrane localization of programmed cell death ligand 1 (PD-L1), an immune checkpoint type I transmembrane glycoprotein, are related to the clinical response of anti-PD-L1/PD-1 therapy. Although the biologically relevant localization of PD-L1 is on the plasma membrane of cancer cells, it has also been reported to be in the cytoplasm and sometimes in the nucleus. Furthermore, it has been claimed that chemotherapeutics can modify PD-L1 expression and/or its nuclear localization.

resultsData from our group suggest that the nuclear localization of PD-L1, and other plasma membrane proteins as well, could be an artifact resulting from inadequate experimental conditions during immunocytochemical studies. Mild detergent and rigorous fixation conditions should be used in order to preserve the membrane localization and to prevent an erroneous translocation of PD-L1 and other non-interconnected membrane proteins, such as CD24, into other cellular compartments including the nucleus, of untreated and chemotherapeutically treated breast cancer cells.

conclusionWe propose that well-specified and rigorously followed protocols should be applied to immunocytochemical diagnostic techniques, especially to those related to individualized diagnosis and treatment.

Indexed as

ArtifactsB7-H1 AntigenBreast NeoplasmsCell Line, TumorCell NucleusDoxorubicinFemaleGlycoproteinsHumansMembrane ProteinsNeoplasmsProtein TransportB7-H1 AntigenDoxorubicinGlycoproteinsMembrane ProteinsBreast cancerDoxorubicinNuclear localizationPD-L1Plasma membrane

Identifiers

PMID30680705
PMCPMC12994297
OpenAlexW2914144393

What Socratic holds

Textmetadata
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 Socratic graph.