Evidence map›Paper›PMID 33011747›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

MHC class I loss in endometrial carcinoma: a potential resistance mechanism to immune checkpoint inhibition.

Lisa A Friedman, Timothy N Bullock, Emily A Sloan, Kari L Ring, Anne M Mills

Abstract read
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-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

24 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The Impact of JAK1 Pathogenic Variants and MHC-I Expression on Response to Immune Checkpoint Inhibition in Endometrial Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  8. Review
  9. Elucidating DNA Damage-Dependent Immune System Activation.International journal of molecular sciences · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Human leukocyte antigen and tumor immunotherapy (Review).International journal of oncology · 2023
    Review
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Lisa A FriedmanDepartment of Pathology, University of Virginia, Charlottesville, VA, USA.
Timothy N BullockDepartment of Pathology, University of Virginia, Charlottesville, VA, USA.
Emily A SloanDepartment of Pathology, Georgetown University, Washington, DC, USA.
Kari L RingDepartment of Obstetrics and Gynecology, University of Virginia, Charlottesville, VA, USA.
Anne M MillsDepartment of Pathology, University of Virginia, Charlottesville, VA, USA. amm7r@virginia.edu.ORCID http://orcid.org/0000-0002-2686-4857
University of Virginia · USGeorgetown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major histocompatibility complex (MHC) class I is a membrane-bound protein complex expressed on nucleated human cells. MHC class I presents intracellular protein fragments to cytotoxic T cells and triggers an activation cascade upon neoantigen detection by these cells. MHC class I loss by tumor cells decreases tumor neoantigen presentation to the immune system and therefore represents a possible mechanism of immunotherapeutic resistance even among cancers that otherwise appear to be good candidates for checkpoint inhibition, such as mismatch repair (MMR)-deficient and PD-L1-positive malignancies. We herein assess MHC class I expression in a range of endometrial carcinomas, including MMR-deficient and PD-L1-positive cancers. Immunohistochemical staining for combined MHC class I A-, B-, and C-heavy chains was performed on 76 cases of endometrial carcinoma and was classified as present, subclonally lost, or diffusely lost. Tumoral PD-L1 expression, PD-L1 combined positive score, and CD3-positive T lymphocytes were also quantified. Forty-two percent of tumors showed loss of MHC class I expression, either in a subclonal (26%) or diffuse (16%) pattern. This included 46% of MMR-deficient and 25% of PD-L1-positive cancers. These findings suggest that tumoral MHC class I status may be an important factor to consider when selecting endometrial cancer patients for checkpoint inhibition.

Indexed as

Drug Resistance, NeoplasmB7-H1 AntigenBiomarkers, TumorCarcinomaCD3 ComplexClinical Decision-MakingDNA Mismatch RepairEndometrial NeoplasmsFemaleHistocompatibility Antigens Class IHumansImmune Checkpoint InhibitorsImmunohistochemistryLymphocytes, Tumor-InfiltratingPredictive Value of TestsTumor MicroenvironmentB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCD3 ComplexHistocompatibility Antigens Class IImmune Checkpoint Inhibitors

Identifiers

PMID33011747
OpenAlexW3091308448

What OpenQuestion 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 OpenQuestion graph.