scholarly journals Correction: Autophagy-related circRNA evaluation reveals hsa_circ_0001747 as a potential favorable prognostic factor for biochemical recurrence in patients with prostate cancer

2021 ◽  
Vol 12 (8) ◽  
Author(s):  
Chuanfan Zhong ◽  
Kaihui Wu ◽  
Shuo Wang ◽  
Zining Long ◽  
Taowei Yang ◽  
...  
2010 ◽  
Vol 106 (11) ◽  
pp. 1623-1627 ◽  
Author(s):  
Jorge R. Caso ◽  
Matvey Tsivian ◽  
Vladimir Mouraviev ◽  
Thomas J. Polascik ◽  
Judd W. Moul

2007 ◽  
Vol 177 (4S) ◽  
pp. 381-382
Author(s):  
Inge M. van Oort ◽  
Dieuwertje E. Kok ◽  
Lambertus A. Kiemeney ◽  
Peter F. Mulders ◽  
J. Alfred Witjes ◽  
...  

Urology ◽  
1999 ◽  
Vol 54 (3) ◽  
pp. 467-472 ◽  
Author(s):  
Jacques Irani ◽  
Jean-Michel Goujon ◽  
Evelyne Ragni ◽  
Laurence Peyrat ◽  
Jacques Hubert ◽  
...  

2021 ◽  
Vol 12 (8) ◽  
Author(s):  
Chuanfan Zhong ◽  
Kaihui Wu ◽  
Shuo Wang ◽  
Zining Long ◽  
Taowei Yang ◽  
...  

AbstractProstate cancer (PCa) is a common high-incidence malignancy in men, some of whom develop biochemical recurrence (BCR) in the advanced stage. However, there are currently no accurate prognostic indicators of BCR in PCa. The aim of our study was to identify an autophagy-related circular RNA prognostic factor of BCR for patients with PCa. In this study, immunochemistry revealed that the classic autophagy marker MAP1LC3B was positively correlated with Gleason score. Least absolute shrinkage and selector operator regression were conducted to develop a novel prognostic model with tenfold cross-validation and an L1 penalty. Five autophagy-related circRNA signatures were included in the prognostic model. Patients with PCa were ultimately divided into high- and low-risk groups, based on the median risk score. Patients with PCa, who had a high risk score, were more likely to develop BCR in a shorter period of time. Univariate and multivariate Cox regression analyses demonstrated that the risk score was an independent variable for predicting BCR in PCa. In addition, a prognostic nomogram integrated with the risk score and numerous clinicopathological parameters was developed to accurately predict 3- and 5-year BCR of patients with PCa. Finally, the hsa_circ_0001747 signature was selected for further experimental verification in vitro and in vivo, which showed that downregulated hsa_circ_0001747 might facilitate PCa via augmenting autophagy. Our findings indicate that the autophagy-related circRNA signature hsa_circ_0001747 may serve as a promising indicator for BCR prediction in patients with PCa.


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