scholarly journals Dynamics of Cancer-Related Proteins in Patients with Bladder Cancer

10.5772/62525 ◽  
2016 ◽  
Author(s):  
Kazumasa Matsumoto ◽  
Morihiro Nishi ◽  
Hideyasu Tsumura ◽  
Ken-ichi Tabata ◽  
Tetsuo Fujita ◽  
...  
2017 ◽  
Vol 95 (5) ◽  
pp. 571-577 ◽  
Author(s):  
Lei Yan ◽  
Yan Wang ◽  
Jun Liang ◽  
Zhixin Liu ◽  
Xiaodong Sun ◽  
...  

We investigated the role of miR-301b in the modulation of the proliferation, migration, and invasion of bladder cancer (BLCA) cells. The expression of miR-301b and EGR1 (early growth response gene 1) mRNA were analyzed by quantitative real-time polymerase chain reaction (qRT-PCR). A dual-luciferase reporter gene system was used to identify the target relationship between miR-301b and EGR1. Cell proliferation, cell cycle, and apoptosis were analyzed by MTT assay, colony-forming assay, and flow cytometry, respectively. Cell motility and invasiveness were assessed by wound healing and Transwell assays. The expression of proteins involved in epithelial-to-mesenchymal transition (EMT) and EGR1 were determined by Western blot. Our results showed that miR-301b was up-regulated while EGR1 was down-regulated in BLCA tissues compared with adjacent normal tissues. The proliferation, migration, and invasiveness of T24 cells (a kind of human BLCA cell) were suppressed by decreasing miR-301b expression or increasing EGR1 expression. In addition, miR-301b promoted EMT signaling by influencing the expression of related proteins. In conclusion, miR-301b promotes the proliferation, migration, and aggressiveness of human BLCA cells by inhibiting the expression of EGR1.


2007 ◽  
Vol 6 (2) ◽  
pp. 120
Author(s):  
M. Kramer ◽  
A.S. Merseburger ◽  
J. Hennenlotter ◽  
A. Stenzl ◽  
M.A. Kuczyk

2006 ◽  
Vol 77 (3) ◽  
pp. 255-263 ◽  
Author(s):  
E. Ioachim ◽  
M. Michael ◽  
M. Salmas ◽  
M.M. Michael ◽  
N.E. Stavropoulos ◽  
...  

Tumor Biology ◽  
2017 ◽  
Vol 39 (3) ◽  
pp. 101042831769118 ◽  
Author(s):  
Hongshuo Zhang ◽  
Yue Fan ◽  
Lingling Xia ◽  
Chunhui Gao ◽  
Xin Tong ◽  
...  

Bladder cancer is the most common cancer of the urinary tract and can be avoided through proper surveillance and monitoring. Several genetic factors are known to contribute to the progression of bladder cancer, many of which produce molecules that serve as cancer biomarkers. Blood, urine, and tissue are commonly analyzed for the presence of biomarkers, which can be derived from either the nucleus or the mitochondria. Recent advances in proteomics have facilitated the high-throughput profiling of data generated from bladder cancer–related proteins or peptides in parallel with high sensitivity and specificity, providing a wealth of information for biomarker discovery and validation. However, the transmission of screening results from one laboratory to another remains the main disadvantage of these methods, a fact that emphasizes the need for consistent and standardized procedures as suggested by the Human Proteome Organization. This review summarizes the latest discoveries and progress of biomarker identification for the early diagnosis, projected prognosis, and therapeutic response of bladder cancer, informs the readers of the current status of proteomic-based biomarker findings, and suggests avenues for future work.


2016 ◽  
Vol 195 (4S) ◽  
Author(s):  
Albert Frances ◽  
Nuria Juanpere ◽  
Judith Penafiel ◽  
Gloria Nohales ◽  
Cristina Camara ◽  
...  

1997 ◽  
Vol 23 (3) ◽  
pp. 141-149 ◽  
Author(s):  
D. S. Tews ◽  
H. H. Goebel ◽  
I. Schneider ◽  
A. Gunkel ◽  
E. Stennert ◽  
...  

Author(s):  
Jessica Marinaro ◽  
Alexander Zeymo ◽  
Jillian Egan ◽  
Filipe Carvalho ◽  
Ross Krasnow ◽  
...  

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