Evidence mapPaperPMID 40327181Full record

ArticleDiscover oncology2025

Lactylation-related risk model for prognostication and therapeutic responsiveness in uterine corpus endometrial carcinoma.

Yupeng Yin, Min Luo

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Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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5 · Who and what money

Authors and funding

2 authors.

Yupeng YinDepartment of Obstetrics and Gynecology, General Hospital of Southern Theatre Command, Guangzhou, 510010, China.
Min LuoDepartment of Obstetrics and Gynecology, General Hospital of Southern Theatre Command, Guangzhou, 510010, China. luomin_2021@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUterine corpus endometrial carcinoma (UCEC) is a prevalent gynecological cancer characterized by varied clinical outcomes and responses to treatment. Developing effective prognostic models is essential for guiding clinical decision-making. Recent research indicates that lactylation-a process impacting gene expression and immune responses-can affect tumor growth, metastasis, and immune evasion through histone modification. This study introduces a lactylation-related risk model aimed at predicting UCEC prognosis and providing insights into treatment efficacy.

methodsWe analyzed transcriptomic data from The Cancer Genome Atlas (TCGA) for UCEC patients and identified two distinct lactylation-related patterns using consensus clustering. A risk model developed using Cox and Lasso regression has been studied for its ability to predict prognosis, immune cell infiltration, and treatment response. Additionally, we investigated the relationship between IGSF1 gene expression and clinical features. Gene Set Enrichment Analysis (GSEA) was performed to explore the function of the IGSF1 gene.

resultsTwo distinct lactylation-related clusters were identified, along with 156 differentially expressed genes between these clusters that are associated with the prognosis of UCEC. A risk model was developed based on three genes: IGSF1, ZFHX4, and SCGB2A1. This model effectively predicts clinical characteristics of UCEC patients, including immune cell infiltration, genetic variations, drug sensitivity, and response to immunotherapy. Notably, IGSF1 is linked to poor prognosis and is associated with immune activity, tumorigenesis, and cancer metabolism.

conclusionsThis study demonstrates that the lactylation-related risk model plays a crucial role in predicting prognosis and the efficacy of immunotherapy in UCEC, offering valuable insights for personalized treatment approaches.

Indexed as

IGSF1ImmunotherapyLactylationRisk modelTherapeutic responsivenessUterine corpus endometrial carcinoma

Identifiers

PMID40327181
PMCPMC12055729

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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 Socratic graph.