Evidence map›Paper›PMID 39095785›Full record

ArticleBMC cancer2024

Results from a real-world study: a novel glycosyltransferase risk score for prognosis, tumor microenvironment phenotypes and immunotherapy in bladder cancer.

Renyu Liu, Ting Yang, Jinyu Huang, Zicheng Xiao, Jinhui Liu, Zhenghao Li, Shiyu Tong

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Renyu LiuDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, China.
Ting YangDepartment of Surgery, Xiangya Hospital, Central South University, Changsha, China.
Jinyu HuangDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, China.
Zicheng XiaoDepartment of Urology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Jinhui LiuDepartment of Urology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Zhenghao LiDepartment of Hepatic biliary pancreatic and spleen surgery, The First Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China. oliverleeee@126.com.
Shiyu TongDepartment of Urology, Xiangya Hospital, Central South University, Changsha, 410008, China. tongshiyu@csu.edu.cn.

Funding

the National Natural Science Foundation of China 8220103844
6 · The paper itself

Abstract

backgroundAlthough immunotherapy shows tremendous potential in the treatment of bladder cancer (BLCA), the overall prognosis and response rates to immunotherapy in BLCA remain suboptimal.

methodsWe performed an extensive evaluation of glycosyltransferase expression patterns in BLCA patients by analyzing 210 glycosyltransferase-related genes. Subsequently, we established correlations between these glycosyltransferase patterns, prognosis, and tumor microenvironment (TME) phenotypes. To offer personalized patient assessments, we developed a glycosyltransferase risk score that accurately predicts prognosis, TME phenotypes, and molecular subtypes. Importantly, we developed a RNA-seq cohort, named Xiangya cohort, to validate our results.

resultsTwo distinct patterns of glycosyltransferase expression were identified, corresponding to inflamed and noninflamed TME phenotypes, and demonstrated the potential to predict prognosis. We developed and validated a comprehensive risk score that accurately predicted individual patient prognosis in the TCGA-BLCA cohort. Additionally, we constructed a nomogram that integrated the risk score with several key clinical factors. Importantly, this risk score was successfully validated in external cohorts, including the Xiangya cohort and GSE48075. Furthermore, we discovered a positive correlation between this risk score and tumor-infiltrating lymphocytes in both the TCGA-BLCA and Xiangya cohorts, suggesting that patients with a higher risk score exhibited an inflamed TME phenotype and were more responsive to immunotherapy. Finally, we observed that the high and low risk score groups were consistent with the luminal and basal subtypes of BLCA, respectively, providing further validation of the risk score's role in the TME in terms of molecular subtypes.

conclusionsGlycosyltransferase patterns exhibit distinct TME phenotypes in BLCA. Our comprehensive risk score provides a promising approach for prognostic prediction and assessment of immunotherapy efficacy, offering valuable guidance for precision medicine.

Indexed as

GlycosyltransferasesImmunotherapyNomogramsPhenotypeTumor MicroenvironmentUrinary Bladder NeoplasmsAgedBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedPrognosisRisk AssessmentBiomarkers, TumorGlycosyltransferasesBladder cancerGlycosyltransferaseImmunotherapyPrognosisTumor microenvironment

Identifiers

PMID39095785
PMCPMC11297740

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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.