Evidence map›Paper›PMID 40410644›Full record

ArticleDiscover oncology2025

Analysis of immune infiltration in basal cell carcinoma based on transcriptome sequencing and experimental validation of diagnostic biomarkers.

Pengfei Fan, Yun Liu, Tengxiao Ma, Qiaoxing Wang, Lei Li

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Pengfei Fan *Department of Plastic and Cosmetic Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.
Yun Liu *Department of Plastic and Cosmetic Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.
Tengxiao MaDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.
Qiaoxing WangDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.
Lei LiDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China. ll18638583636@163.com.

Funding

Education Department of Hainan Province Hnky2025ZC-5Hainan Medical University S202411810029
6 · The paper itself

Abstract

backgroundBasal cell carcinoma (BCC) is the most common type of malignant skin tumour, and its incidence is increasing worldwide. While it grows slowly, BCC is locally invasive, causing significant tissue damage. This study investigated the role of mRNAs in BCC through bioinformatics and experimental validation to elucidate the molecular mechanisms involved.

methodsDifferentially expressed genes (DEGs) were identified from the transcriptome data of 30 BCC patients and 16 controls from the GSE7553, GSE103439, and GSE42109 datasets. Gene Ontology and KEGG analyses were performed to explore gene expression and pathways. A protein‒protein interaction (PPI) network was constructed to identify hub genes, and immune cell infiltration was analysed to study the tumour microenvironment. The diagnostic potential of target genes (LEF1, LGR5, and SOX4) was assessed using ROC curves. Gene expression was validated with qPCR and Western blotting.

resultsA total of 135 DEGs were identified, with 9 hub genes selected. LEF1, LGR5, and SOX4 showed strong diagnostic potential, with AUC values of 0.888, 0.955, and 0.996, respectively. The immune cell analysis revealed increased numbers of B cells, NK cells, and T cells in BCC, whereas the numbers of DCs, pDCs, and Treg cells were reduced. qPCR and Western blotting confirmed increased LEF1 and LGR5 expression in BCC. SOX4 expression was increased according to the qPCR results but was not significantly elevated according to the Western blot results, warranting further validation.

conclusionsLEF1, LGR5, and SOX4 may play roles in BCC pathogenesis and could serve as diagnostic biomarkers. These findings provide insights into BCC development and support future research for improved detection and treatment.

Indexed as

Basal cell carcinomaDiagnostic biomarkersImmune infiltration

Identifiers

PMID40410644
PMCPMC12102445

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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.