Abstract

The progression from non-muscle-invasive bladder cancer (NMIBC) to muscle-invasive bladder cancer (MIBC) increases the risk of death. It is therefore important to find new relevant molecular models that will allow for effective prediction of the progression and prognosis of bladder cancer (BC). Using RNA-Sequence data of 49 BC patients in Shanghai tenth people’s hospital (STPH) and weighted gene co-expression network analysis methods, a co-expression network of genes was developed and three key modules associated with malignant progression were selected. Based on the genes in three key modules, an eight-gene risk signature was established using univariate Cox regression and the Least absolute shrinkage and selection operator Cox model in The Cancer Genome Atlas Program (TCGA) and validated in validation sets. Subsequently, a nomogram based on the risk signature was constructed for prognostic prediction. The mRNA and protein expression levels of eight genes in cell lines and tissues were further investigated. The novel eight-gene risk signature was closely related to the malignant clinical features of BC and could predict the prognosis of patients in the training dataset (TCGA) and four validation sets (GSE32894, GSE13507, IMvigor210 trial, and STPH). The nomogram showed good prognostic prediction and calibration. The mRNA and protein expression levels of the eight genes were differentially expressed in cell lines and tissues. In our study, we established a novel eight-gene risk signature that could predict the progression and prognoses of BC patients.

Highlights

  • Bladder cancer (BC) is ranked 4th as the most commonly diagnosed cancer in men [1]

  • A total of 49 bladder cancer (BC) patients (35 non-muscle-invasive bladder cancer (NMIBC) and 14 muscle-invasive bladder cancer (MIBC)) from Shanghai tenth people’s hospital (STPH) were enrolled for the study

  • 2,725 DEGs were identified between NMIBC and MIBC

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Summary

Introduction

Bladder cancer (BC) is ranked 4th as the most commonly diagnosed cancer in men [1]. >30% of patients with NMIBC develop recurrence and progresses to MIBC within 5 years after diagnosis [2]. Many clinical index models and non-invasive marker tests to predict the recurrence and progression of BC have been investigated extensively in recent years. Some previous risk signatures were constructed based on the gene microarray that contains limited expression levels of genes, which may limit the performance of the risk signatures. For these reasons, it is important to identify valuable models or biomarkers for evaluating the prognosis and monitor the progression of BC

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