Understanding the biology of urothelial cancer metastasis

被引:16
作者
Kobayashi, Takashi [1 ]
机构
[1] Kyoto Univ, Dept Urol, Grad Sch Med, Kyoto, Japan
基金
日本学术振兴会;
关键词
Urothelial carcinoma; Metastasis; Epithelial-mesenchymal transition; Animal models;
D O I
10.1016/j.ajur.2016.09.005
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Management of unresectable urothelial cancer (UC) has been a clinical challenge for decades. While drug resistance is a key issue, precise understanding of biology of UC metastasis is another challenge for the improvement of treatment outcome of UC patients. Introduction of the cell biology concepts including epithelial-mesenchymal transition (EMT) and cancer stemness seems to explain UC metastasis. Molecular genetics based on gene expression profiling, next generation sequencing, and explosion of non-coding RNA world has opened the door to intrinsic molecular subtyping of UC. Next steps include, based on the recently accumulated understanding, the establishment of novel disease models representing UC metastasis in various experimental platforms, particularly in vivo animal systems. Indeed, novel knowledge molecular genetics has not been fully linked to the modeling of UC metastasis. Further understanding of bladder carcinogenesis is needed particularly with regard to cell of origin related to tumor characteristics including driver gene alterations, pathological differentiations, and metastatic ability. Then we will be able to establish better disease models, which will consequently lead us to further understanding of biology and eventually the development of novel therapeutic strategies for UC metastasis. (C) 2016 Editorial Office of Asian Journal of Urology. Production and hosting by Elsevier B.V.
引用
收藏
页码:211 / 222
页数:12
相关论文
共 154 条
[1]   miR-200 Expression Regulates Epithelial-to-Mesenchymal Transition in Bladder Cancer Cells and Reverses Resistance to Epidermal Growth Factor Receptor Therapy [J].
Adam, Liana ;
Zhong, Meng ;
Choi, Woonyoung ;
Qi, Wei ;
Nicoloso, Milena ;
Arora, Ameeta ;
Calin, George ;
Wang, Hua ;
Siefker-Radtke, Arlene ;
McConkey, David ;
Bar-Eli, Menashe ;
Dinney, Colin .
CLINICAL CANCER RESEARCH, 2009, 15 (16) :5060-5072
[2]   In vitro and in vivo inhibitory effect of three Cox-2 inhibitors and epithelial-to-mesenchymal transition in human bladder cancer cell lines [J].
Adhim, Z. ;
Matsuoka, T. ;
Bito, T. ;
Shigemura, K. ;
Lee, K-M ;
Kawabata, M. ;
Fujisawa, M. ;
Nibu, K. ;
Shirakawa, T. .
BRITISH JOURNAL OF CANCER, 2011, 105 (03) :393-402
[3]   GON4L Drives Cancer Growth through a YY1-Androgen Receptor-CD24 Axis [J].
Agarwal, Neeraj ;
Dancik, Garrett M. ;
Goodspeed, Andrew ;
Costello, James C. ;
Owens, Charles ;
Duex, Jason E. ;
Theodorescu, Dan .
CANCER RESEARCH, 2016, 76 (17) :5175-5185
[4]   Frequent somatic CDH1 loss-of-function mutations in plasmacytoid variant bladder cancer [J].
Al-Ahmadie, Hikmat A. ;
Iyer, Gopa ;
Lee, Byron H. ;
Scott, Sasinya N. ;
Mehra, Rohit ;
Bagrodia, Aditya ;
Jordan, Emmet J. ;
Gao, Sizhi Paul ;
Ramirez, Ricardo ;
Cha, Eugene K. ;
Desai, Neil B. ;
Zabor, Emily C. ;
Ostrovnaya, Irina ;
Gopalan, Anuradha ;
Chen, Ying-Bei ;
Fine, Samson W. ;
Tickoo, Satish K. ;
Gandhi, Anupama ;
Hreiki, Joseph ;
Viale, Agnss ;
Arcila, Maria E. ;
Dalbagni, Guido ;
Rosenberg, Jonathan E. ;
Bochner, Bernard H. ;
Bajorin, Dean F. ;
Berger, Michael F. ;
Reuter, Victor E. ;
Taylor, Barry S. ;
Solit, David B. .
NATURE GENETICS, 2016, 48 (04) :356-+
[5]   The chemoinvasion assay: a method to assess tumor and endothelial cell invasion and its modulation [J].
Albini, Adriana ;
Benelli, Roberto .
NATURE PROTOCOLS, 2007, 2 (03) :504-511
[6]   Histological variants of urothelial carcinoma: diagnostic, therapeutic and prognostic implications [J].
Amin, Mahul B. .
MODERN PATHOLOGY, 2009, 22 :S96-S118
[7]   Role of the microtubule-targeting drug vinflunine on cell-cell adhesions in bladder epithelial tumour cells [J].
Aparicio L.A. ;
Castosa R. ;
Haz-Conde M. ;
Rodríguez M. ;
Blanco M. ;
Valladares M. ;
Figueroa A. .
BMC Cancer, 14 (1)
[8]   Cell-penetrating D-Isomer Peptides of p53 C-terminus: Long-term Inhibitory Effect on the Growth of Bladder Cancer [J].
Araki, Daiji ;
Takayama, Kentaro ;
Inoue, Miyabi ;
Watanabe, Toyohiko ;
Kumon, Hiromi ;
Futaki, Shiroh ;
Matsui, Hideki ;
Tomizawa, Kazuhito .
UROLOGY, 2010, 75 (04) :813-819
[9]   OCT-4, an embryonic stem cell marker, is highly expressed in bladder cancer [J].
Atlasi, Yaser ;
Mowla, Seyed J. ;
Ziaee, Seyed A. M. ;
Bahrami, Ahmad-Reza .
INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (07) :1598-1602
[10]   Patient-derived bladder cancer xenografts: a systematic review [J].
Bernardo, Carina ;
Costa, Ceu ;
Sousa, Nuno ;
Amado, Francisco ;
Santos, Locio .
TRANSLATIONAL RESEARCH, 2015, 166 (04) :324-331