Evidence map›Paper›PMID 35892887›Full record

ReviewCancers2022

The Contributions of Cancer-Testis and Developmental Genes to the Pathogenesis of Keratinocyte Carcinomas.

Brandon Ramchatesingh, Jennifer Gantchev, Amelia Martínez Villarreal, Raman Preet Kaur Gill, Marine Lambert, Sriraam Sivachandran, Philippe Lefrançois, Ivan V Litvinov

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Special Issue "Molecular Research and Cellular Biology of Breast Cancer".International journal of molecular sciences · 2026
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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

8 authors at 1 institution in 1 country.

Brandon RamchatesinghDivision of Experimental Medicine, McGill University, Montreal, QC H4A 3J1, Canada.
Jennifer GantchevDivision of Experimental Medicine, McGill University, Montreal, QC H4A 3J1, Canada.
Amelia Martínez VillarrealDivision of Experimental Medicine, McGill University, Montreal, QC H4A 3J1, Canada.
Raman Preet Kaur GillCancer Research Program, Research Institute of the McGill University Health Center, Montreal, QC H4A 3J1, Canada.
Marine LambertCancer Research Program, Research Institute of the McGill University Health Center, Montreal, QC H4A 3J1, Canada.
Sriraam SivachandranDivision of Experimental Medicine, McGill University, Montreal, QC H4A 3J1, Canada.
Philippe LefrançoisDivision of Dermatology, McGill University Health Center, Montreal, QC H4A 3J1, Canada.ORCID 0000-0003-2939-7956
Ivan V LitvinovDivision of Experimental Medicine, McGill University, Montreal, QC H4A 3J1, Canada.ORCID 0000-0003-0562-4675
McGill University Health Centre · CA

Funding

CIHR 426655Consejo Nacional de Ciencia y Tecnología N/AFonds de la recherche du Québec-Santé #34753, #36769 and #296643
6 · The paper itself

Abstract

Keratinocyte carcinomas are among the most prevalent malignancies worldwide. Basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (cSCC) are the two cancers recognized as keratinocyte carcinomas. The standard of care for treating these cancers includes surgery and ablative therapies. However, in recent years, targeted therapies (e.g., cetuximab for cSCC and vismodegib/sonidegib for BCC) have been used to treat advanced disease as well as immunotherapy (e.g., cemiplimab). These treatments are expensive and have significant toxicities with objective response rates approaching ~50-65%. Hence, there is a need to dissect the molecular pathogenesis of these cancers to identify novel biomarkers and therapeutic targets to improve disease management. Several cancer-testis antigens (CTA) and developmental genes (including embryonic stem cell factors and fetal genes) are ectopically expressed in BCC and cSCC. When ectopically expressed in malignant tissues, functions of these genes may be recaptured to promote tumorigenesis. CTAs and developmental genes are emerging as important players in the pathogenesis of BCC and cSCC, positioning themselves as attractive candidate biomarkers and therapeutic targets requiring rigorous testing. Herein, we review the current research and offer perspectives on the contributions of CTAs and developmental genes to the pathogenesis of keratinocyte carcinomas.

Indexed as

basal cell carcinomabiomarkerscancer/testis antigencutaneous squamous cell carcinomaembryonic stem celloncofetal antigenprecision oncology

Identifiers

PMID35892887
PMCPMC9367444
OpenAlexW4288042207

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.