Evidence map›Paper›PMID 38188285›Full record

ArticleFrontiers in oncology2023

A tumor-restricted glycoform of podocalyxin is a highly selective marker of immunologically cold high-grade serous ovarian carcinoma.

Julyanne Brassard, Michael R Hughes, Pamela Dean, Diana Canals Hernaez, Shelby Thornton, Allyson C Banville, Julian Smazynski, Mary Warren, Kevin Zhang, Katy Milne and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

16 authors at 3 institutions in 1 country.

Julyanne BrassardSchool of Biomedical Engineering, University of British Columbia, Vancouver, BC, Canada.
Michael R HughesSchool of Biomedical Engineering, University of British Columbia, Vancouver, BC, Canada.
Pamela DeanDepartment of Cellular and Physiological Sciences, University of British Columbia, Vancouver, BC, Canada.
Diana Canals HernaezSchool of Biomedical Engineering, University of British Columbia, Vancouver, BC, Canada.
Shelby ThorntonMolecular and Advanced Pathology Core (MAPcore), University of British Columbia, Vancouver, BC, Canada.
Allyson C BanvilleBritish Columbia Cancer Agency, Victoria, BC, Canada.
Julian SmazynskiBritish Columbia Cancer Agency, Victoria, BC, Canada.
Mary WarrenBritish Columbia Cancer Agency, Victoria, BC, Canada.
Kevin ZhangBritish Columbia Cancer Agency, Victoria, BC, Canada.
Katy MilneBritish Columbia Cancer Agency, Victoria, BC, Canada.
C Blake GilksDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Anne-Marie Mes-MassonCentre de Recherche du Centre hospitalier de l'Université de Montréal, Montreal, QC, Canada.
David G HuntsmanMolecular and Advanced Pathology Core (MAPcore), University of British Columbia, Vancouver, BC, Canada.
Brad H NelsonBritish Columbia Cancer Agency, Victoria, BC, Canada.
Calvin D RoskelleyDepartment of Cellular and Physiological Sciences, University of British Columbia, Vancouver, BC, Canada.
Kelly M McNagnySchool of Biomedical Engineering, University of British Columbia, Vancouver, BC, Canada.
University of British Columbia · CABC Cancer Agency · CACentre Hospitalier de l’Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Targeted-immunotherapies such as antibody-drug conjugates (ADC), chimeric antigen receptor (CAR) T cells or bispecific T-cell engagers (eg, BiTE Methods: In this study we characterize these PODO447-expressing tumors as a distinct subset of HGSOC using four different patient cohorts that include pre-chemotherapy, post-neoadjuvant chemotherapy (NACT) and relapsing tumors as well as tumors from various peritoneal locations. Results: We find that the PODO447 epitope expression is similar across tumor locations and negligibly impacted by chemotherapy. Invariably, tumors with high levels of the PODO447 epitope lack infiltrating CD8 Discussion: We conclude that the PODO447 glycoepitope is an excellent biomarker of immune "cold" tumors and a candidate for the development of targeted-therapies for these hard-to-treat cancers.

Indexed as

glycoepitopehigh-grade serous ovarian carcinomaimmune coldimmunotherapypodocalyxin

Identifiers

PMID38188285
PMCPMC10771318
OpenAlexW4390057292

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.