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pmid:35877232

Molecular Differences between Squamous Cell Carcinoma and Adenocarcinoma Cervical Cancer Subtypes: Potential Prognostic Biomarkers.

Alma D Campos-Parra · Milagros Pérez-Quintanilla · Antonio Daniel Martínez-Gutierrez · Delia Pérez-Montiel · Jaime Coronel-Martínez · Oliver Millan-Catalan · David Cantú De León · Carlos Pérez-Plasencia

Current oncology (Toronto, Ont.) · 2022 doi:10.3390/curroncol29070372

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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title
Molecular Differences between Squamous Cell Carcinoma and Adenocarcinoma Cervical Cancer Subtypes: Potential Prognostic Biomarkers.
doi
10.3390/curroncol29070372
pmid
35877232
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[0]
Alma D Campos-Parra
[1]
Milagros Pérez-Quintanilla
[2]
Antonio Daniel Martínez-Gutierrez
[3]
Delia Pérez-Montiel
[4]
Jaime Coronel-Martínez
[5]
Oliver Millan-Catalan
[6]
David Cantú De León
[7]
Carlos Pérez-Plasencia
journal
Current oncology (Toronto, Ont.)
year
2022
abstract
The most frequently diagnosed histological types of cervical cancer (CC) are squamous cell carcinoma (SCC) and adenocarcinoma (ADC). Clinically, the prognosis of both types is controversial. A molecular profile that distinguishes each histological subtype and predicts the prognosis would be of great benefit to CC patients. METHODS: The transcriptome of CC patients from The Cancer Genome Atlas (TCGA) was analyzed using the DESeq2 package to obtain the differentially expressed genes (DEGs) between ADC and SCC. The DEGs were validated on a publicly available Mexican-Mestizo patient transcriptome dataset (GSE56303). The global biological pathways involving the DEGs were obtained using the Webgestalt platform. The associations of the DEGs with Overall Survival (OS) were assessed. Finally, three DEGs were validated by RT-qPCR in an independent cohort of Mexican patients. RESULTS: The molecular profiles of ADC and SCC of the CC patients of the TCGA database and the Mexican-Mestizo cohort (GSE56303) were determined obtaining 1768 and 88 DEGs, respectively. Strikingly, 70 genes were concordant-with similar Log2FoldChange values-in both cohorts. The 70 DEGs were involved in IL-17, JAK/STAT, and Ras signaling. Kaplan-Meier OS analysis from the Mexican-Mestizo cohort showed that higher GABRB2 and TSPAN8 and lower TMEM40 expression were associated with better OS. Similar results were found in an independent Mexican cohort. CONCLUSIONS: Molecular differences were detected between the ADC and SCC subtypes; however, further studies are required to define the appropriate prognostic biomarker for each histological type.
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Differential expression analysis was carried out using the DESeq2 package [20], where an adjusted (adj) p-value < 0.01 and a log2FoldChange >2 or <2 were considered significant.
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Differential expression analysis was carried out using the DESeq2 package [20], where an adjusted (adj) p-value < 0.01 and a log2FoldChange >2 or <2 were considered significant.
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The transcriptome of CC patients from The Cancer Genome Atlas (TCGA) was analyzed using the DESeq2 package to obtain the differentially expressed genes (DEGs) between ADC and SCC.
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The transcriptome of CC patients from The Cancer Genome Atlas (TCGA) was analyzed using the DESeq2 package to obtain the differentially expressed genes (DEGs) between ADC and SCC.
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Strikingly, 70 genes were concordant—with similar Log2FoldChange values—in both cohorts.
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The transcriptome of CC patients from The Cancer Genome Atlas (TCGA) was analyzed using the DESeq2 package to obtain the differentially expressed genes (DEGs) between ADC and SCC.
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Genome wide expression profile in cervical cancer patients (staged, locally advanced)
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35877232", "kind": "science-record", "revision": 5, "content_hash": "sha256:28958ad5d5a6cecd8957fab33b88dd19ff05b3bcaf37406e6cb9e05103ca4886", "created_at": "2026-11-01T18:14:58Z", "updated_at": "2026-11-01T22:49:38Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Molecular Differences between Squamous Cell Carcinoma and Adenocarcinoma Cervical Cancer Subtypes: Potential Prognostic Biomarkers.", "doi": "10.3390/curroncol29070372", "pmid": "35877232", "authors": ["Alma D Campos-Parra", "Milagros Pérez-Quintanilla", "Antonio Daniel Martínez-Gutierrez", "Delia Pérez-Montiel", "Jaime Coronel-Martínez", "Oliver Millan-Catalan", "David Cantú De León", "Carlos Pérez-Plasencia"], "journal": "Current oncology (Toronto, Ont.)", "year": 2022, "abstract": "The most frequently diagnosed histological types of cervical cancer (CC) are squamous cell carcinoma (SCC) and adenocarcinoma (ADC). Clinically, the prognosis of both types is controversial. A molecular profile that distinguishes each histological subtype and predicts the prognosis would be of great benefit to CC patients.\nMETHODS: The transcriptome of CC patients from The Cancer Genome Atlas (TCGA) was analyzed using the DESeq2 package to obtain the differentially expressed genes (DEGs) between ADC and SCC. The DEGs were validated on a publicly available Mexican-Mestizo patient transcriptome dataset (GSE56303). The global biological pathways involving the DEGs were obtained using the Webgestalt platform. The associations of the DEGs with Overall Survival (OS) were assessed. Finally, three DEGs were validated by RT-qPCR in an independent cohort of Mexican patients.\nRESULTS: The molecular profiles of ADC and SCC of the CC patients of the TCGA database and the Mexican-Mestizo cohort (GSE56303) were determined obtaining 1768 and 88 DEGs, respectively. Strikingly, 70 genes were concordant-with similar Log2FoldChange values-in both cohorts. The 70 DEGs were involved in IL-17, JAK/STAT, and Ras signaling. Kaplan-Meier OS analysis from the Mexican-Mestizo cohort showed that higher GABRB2 and TSPAN8 and lower TMEM40 expression were associated with better OS. Similar results were found in an independent Mexican cohort.\nCONCLUSIONS: Molecular differences were detected between the ADC and SCC subtypes; however, further studies are required to define the appropriate prognostic biomarker for each histological type.", "claims": [{"id": "claim-method", "statement": "Differential expression analysis was carried out using the DESeq2 package [20], where an adjusted (adj) p-value < 0.01 and a log2FoldChange >2 or <2 were considered significant.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35877232", "locator": "sections[3] \"2.1. 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