The role of LIM and SH3 protein-1 in bladder cancer metastasis

被引:1
作者
Sato, Misaki [1 ]
Yoneyama, Mihoko Sutoh [1 ,2 ]
Hatakeyama, Shingo [2 ]
Funyu, Tomihisa [1 ]
Suzuki, Tadashi [1 ]
Ohyama, Chikara [2 ]
Tsuboi, Shigeru [1 ,2 ]
机构
[1] Oyokyo Kidney Res Inst, Dept Canc Immunol & Cell Biol, 90 Kozawa Yamazaki, Hirosaki, Aomori 0368243, Japan
[2] Hirosaki Univ, Grad Sch Med, Dept Urol, Hirosaki, Aomori 0368562, Japan
关键词
LIM and SH3 protein; LASP-1; bladder cancer; metastasis; invadopodia; INVADOPODIA FORMATION; CELL; LASP-1; MIGRATION; PROLIFERATION; INVASION;
D O I
10.3892/ol.2017.6802
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The LIM and SH3 protein-1 ( LASP-1) is a multi-domain protein that is involved in several malignant cancers. The role of LASP-1 in malignant phenotypes including high invasive properties and unrestricted cell proliferation, remain to be elucidated. The present study reported the association of LASP-1 expression with bladder cancer malignancy and its role in cancer cell invasion and proliferation. The immunohistochemical analysis of the expression status of LASP-1 in radical cystectomy specimens from invasive bladder cancer patients revealed that the LASP-1-positive patients demonstrated a decreased survival rate compared with the LASP-1-negative patients. The expression level of LASP-1 was increased in invasive bladder cancer cell lines compared with the non-invasive bladder cancer cell lines. Invasive cancer cells form invadopodia, the filamentous actin-based membrane protrusions that are essential in cancer cell invasion. Knockdown of LASP-1 reduced the ability to form invadopodia, resulting in decreased invasive capacity of the LASP-1 knockdown cells. In addition, knockdown of LASP-1 reduced cell proliferation. These results suggest that LASP-1 is important in invadopodia formation and cell proliferation of bladder cancer cells, promoting the malignant properties and resulting in poor-prognosis.
引用
收藏
页码:4829 / 4834
页数:6
相关论文
共 28 条
[1]   LASP-1, a Novel Urinary Marker for Detection of Bladder Cancer [J].
Ardelt, Peter ;
Gruenemay, Nadine ;
Strehl, Annette ;
Jilg, Cordula ;
Miernik, Arkadius ;
Kneitz, Burkhard ;
Butt, Elke .
UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2013, 31 (08) :1591-1598
[2]   Perioperative Chemotherapy for Muscle-Invasive Bladder Cancer [J].
Booth, Christopher M. ;
Siemens, D. Robert ;
Li, Gavin ;
Peng, Yingwei ;
Tannock, Ian F. ;
Kong, Weidong ;
Berman, David M. ;
Mackillop, William J. .
CANCER, 2014, 120 (11) :1630-1638
[3]   CELL AND MOLECULAR BIOLOGY OF INVADOPODIA [J].
Caldieri, Giusi ;
Ayala, Inmaculacla ;
Attanasio, Francesca ;
Buccione, Roberto .
INTERNATIONAL REVIEW OF CELL AND MOLECULAR BIOLOGY, VOL 275, 2009, 275 :1-34
[4]   Lasp-1 is a regulated phosphoprotein within the cAMP signaling pathway in the gastric parietal cell [J].
Chew, CS ;
Parente, JA ;
Zhou, CJ ;
Baranco, E ;
Chen, X .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 275 (01) :C56-C67
[5]   Cell migration in 3D matrix [J].
Even-Ram, S ;
Yamada, KM .
CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (05) :524-532
[6]   Overexpression of LASP-1 mediates migration and proliferation of human ovarian cancer cells and influences zyxin localisation [J].
Grunewald, T. G. P. ;
Kammerer, U. ;
Winkler, C. ;
Schindler, D. ;
Sickmann, A. ;
Honig, A. ;
Butt, E. .
BRITISH JOURNAL OF CANCER, 2007, 96 (02) :296-305
[7]   Silencing of LASP-1 influences zyxin localization, inhibits proliferation and reduces migration in breast cancer cells [J].
Grunewald, TGP ;
Kammerer, U ;
Schulze, E ;
Schindler, D ;
Honig, A ;
Zimmer, M ;
Butt, E .
EXPERIMENTAL CELL RESEARCH, 2006, 312 (07) :974-982
[8]   The LIM and SH3 domain protein family: structural proteins or signal transducers or both? [J].
Grunewald, Thomas G. P. ;
Butt, Elke .
MOLECULAR CANCER, 2008, 7 (1)
[9]  
HISAZUMI H, 1981, UROL RES, V9, P231
[10]   Invadopodia are essential in transurothelial invasion during the muscle invasion of bladder cancer cells [J].
Imanishi, Kengo ;
Yoneyama, Mihoko Sutoh ;
Hatakeyama, Shingo ;
Yamamoto, Hayato ;
Koie, Takuya ;
Saitoh, Hisao ;
Yamaya, Kanemitsu ;
Funyu, Tomihisa ;
Nakamura, Toshiya ;
Ohyama, Chikara ;
Tsuboi, Shigeru .
MOLECULAR MEDICINE REPORTS, 2014, 9 (06) :2159-2165