Evidence map›Paper›PMID 40873284›Full record

ArticleCurrent medicinal chemistry2026

Expression of TCEAL2 is a Novel Prognostic Biomarker and Potential Therapeutic Target in Cervical Squamous Cell Carcinoma and Endocervical Adenocarcinoma.

Jinyuan Li, Zhen Ye, Yuhong Gan, Dongbing Li, Yibiao Chen

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Article in Current medicinal chemistry, 2026. 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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5 · Who and what money

Authors and funding

5 authors.

Jinyuan LiPelvic Radiotherapy Department, Meizhou People's Hospital, Meizhou, 514031, Guangdong, China.ORCID 0009-0002-4341-6383
Zhen YeDepartment of Pathology, Meizhou People's Hospital, Meizhou, 514031, Guangdong, China.ORCID 0009-0004-9626-7849
Yuhong GanDepartment of Clinical Pharmacy, Meizhou People's Hospital, Meizhou, 514031, Guangdong, China.ORCID 0009-0009-0240-7983
Dongbing LiPelvic Radiotherapy Department, Meizhou People's Hospital, Meizhou, 514031, Guangdong, China.ORCID 0000-0002-5227-9643
Yibiao ChenThoracic and Abdominal Radiotherapy Department I, Meizhou People's Hospital, Meizhou, 514031, Guangdong, China.ORCID 0000-0002-9268-4950

Funding

Guangdong Medical Science and Technology Research Fund Project B2021145Meizhou People's Hospital Scientific Research and Cultivation Project PY-C2019018
6 · The paper itself

Abstract

backgroundCervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) are major gynecological malignancies, causing significant cancer-related deaths in women. Current treatments yield poor outcomes, with a 5-year survival rate of only 17%. Identifying new biomarkers and therapeutic targets is crucial for improving prognosis and guiding personalized treatments.

methodsWe analyzed TCEAL2 expression using data from The Cancer Genome Atlas (TCGA) across various cancers, including CESC. We explored its correlation with clinical features, prognosis, immune infiltration, MSI, mRNAsi, and drug sensitivity. TCEAL2 expression was validated in GSE9750 datasets and CESC cell lines using qRT-PCR.

resultsTCEAL2 expression was significantly dysregulated in CESC. Elevated TCEAL2 levels correlated with poor clinical outcomes, including advanced pathological M stage (p = 0.009), initial treatment failure (p = 0.0098), and reduced overall survival (OS) (p = 0.013). TCEAL2 was an independent predictor of unfavorable OS (p = 0.032). It was associated with key pathways such as calcium signaling, oxidative phosphorylation, and Wnt signaling. TCEAL2 also correlated with immune cell infiltration, MSI, and mRNAsi. Notably, TCEAL2 levels inversely correlated with sensitivity to several drugs, including CAY10603 and SB-223133. DISCUSSION: The results suggest that TCEAL2 plays a significant role in CESC progression and its tumor microenvironment. Its correlation with immune infiltration and drug sensitivity highlights its potential as a prognostic biomarker and therapeutic target. Future studies should focus on elucidating the molecular mechanisms and validating their clinical utility.

conclusionTCEAL2 is a potential prognostic biomarker and therapeutic target in CESC. Further research is needed to explore its role and clinical applications.

Indexed as

AdenocarcinomaBiomarkers, TumorCarcinoma, Squamous CellUterine Cervical NeoplasmsAntineoplastic AgentsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansPrognosisAntineoplastic AgentsBiomarkers, TumorCervical squamous cell carcinomadrug sensitivity.endocervical adenocarcinomaimmune infiltrationmRNAsiprognosisTCEAL2

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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.