E2F3/5/8 serve as potential prognostic biomarkers and new therapeutic direction for human bladder cancer

Author:

Gan Zhilu1,Abudurexiti Alimujiang1,Hu Xiaogang1,Chen Wenxin1,Zhang Ning1,Sang Wei23

Affiliation:

1. Surgery Department of Urology, The Third People’s Hospital of Xinjiang Uyghur Autonomous Region, Urumqi, P.R. China

2. Department of Pathology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, P.R. China

3. Department of Pathology, The First Affiliated Hospital of Xinjiang Medical University, State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Urumqi, P.R. China.

Abstract

Objects: Human bladder cancer (BC) is the most common urogenital system malignancy. E2F transcription factors (E2Fs) have been reported to be involved in the growth of various cancers. However, the expression patterns, prognostic value and immune infiltration in the tumor microenvironment of the 8 E2Fs in BC have yet fully to be explored. Methods and strategy: We investigated the differential expression of E2Fs in BC patients, the prognostic value and correlation with immune infiltration by analyzing a range of databases. Results: We found that the mRNA expression levels of E2F1/2/3/4/5/7/8 were significantly higher in BC patients than that of control tissues. And the increased mRNA expression levels of all E2Fs were associated with tumor stage of BC. The survival analysis revealed that the elevated mRNA expression levels of E2F3/5/8 were significantly correlated with the overall survival (OS) of BC patients. And the genetic changes of E2Fs in BC patients were associated with shorter overall survival (OS) and progression-free survival (PFS). In addition, we revealed that the E2F3/5/8 expressions were closely correlated with tumor-infiltrating lymphocytes (TILs). Conclusions: E2F3/5/8 might serve as promising prognostic biomarkers and new therapeutic direction for BC patients.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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