Evidence map›Paper›PMID 39207605›Full record

ArticleDiscover oncology2024

BCAM (basal cell adhesion molecule) protein expression in different tumor populations.

Sneha Burela, Mengni He, Ioannis P Trontzas, Niki Gavrielatou, Kurt A Schalper, Solomon Langermann, Dallas B Flies, David L Rimm, Thazin N Aung

Abstract read
In one paragraph

Article in Discover oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
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  5. 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

9 authors.

Sneha BurelaDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA.
Mengni HeDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA.
Ioannis P TrontzasDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA.
Niki GavrielatouSchool of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Kurt A SchalperDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA.
Solomon LangermannNextCure Inc, Beltsville, MD, USA.
Dallas B FliesNextCure Inc, Beltsville, MD, USA.
David L RimmDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA. david.rimm@yale.edu.
Thazin N AungDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06519, USA. thazin.aung@yale.edu.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863NextCure.Inc SRA
6 · The paper itself

Abstract

Basal Cell Adhesion Molecule (BCAM), a receptor for laminin subunit α5, plays a crucial role in the pathogenesis of various malignancies. Notably, evidence of hypermethylation at multiple immune checkpoints in patients with low BCAM expression suggests these individuals may respond favorably to immunotherapy using ICIs (immune checkpoint inhibitors). This finding lays the foundation for the hypothesis that BCAM may serve as an important biomarker in cancer patients. To investigate this potential, we evaluated BCAM expression patterns in 3114 patients from both discovery and validation cohorts, spanning seven cancer types, using quantitative immunofluorescence (QIF). We also explored the correlation between BCAM and PD-L1 expressions within these cohorts, aiming to establish its potential predictive value for immunotherapy response. Our findings indicate that BCAM was highly expressed in ovarian (79.2%) and lung (78.5%) tumors, with lower yet significant expression in breast (37.7%), head and neck (31.3%), and bladder-urothelial tumors (27.6%). Notably, high BCAM expression was associated with better OS in NSCLC. More importantly, BCAM expression did not correlate with PD-L1 protein expression in any of these tumors, highlighting its independent predictive potential. The widespread expression of BCAM across multiple tumor types, coupled with its lack of correlation with PD-L1 expression, highlights its potential as a predictive novel biomarker across various cancer types.

Indexed as

Cancer biomarkersPD-L1 expressionQuantitative immunofluorescence (QIF)The basal cell adhesion molecule (BCAM)Therapeutic target

Identifiers

PMID39207605
PMCPMC11362396

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Registered trials

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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.