Expression and clinical significance of Wee1 in colorectal cancer

被引:17
作者
Egeland, Eivind Valen [1 ]
Flatmark, Kjersti [1 ,2 ,3 ]
Nesland, Jahn M. [3 ,4 ]
Florenes, Vivi Ann [4 ]
Maelandsmo, Gunhild M. [1 ,5 ]
Boye, Kjetil [1 ,6 ]
机构
[1] Oslo Univ Hosp, Inst Canc Res, Norwegian Radium Hosp, Dept Tumor Biol, POB 4953, NO-0424 Oslo, Norway
[2] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Surg Gastroenterol, Oslo, Norway
[3] Univ Oslo, Fac Med, Oslo, Norway
[4] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Pathol, Oslo, Norway
[5] Univ Tromso, Dept Pharm, Fac Hlth Sci, Tromso, Norway
[6] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Oncol, Oslo, Norway
关键词
Wee1; S100A4; Colorectal cancer; Prognostic marker; COLON-CANCER; THYMIDYLATE SYNTHASE; MITOTIC CATASTROPHE; PROGNOSTIC MARKER; PROTEIN S100A4; NUCLEAR S100A4; CYCLIN B1; IN-VIVO; KINASE; CELLS;
D O I
10.1007/s13277-016-5081-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Wee1 is a nuclear kinase regulating cell cycle progression, and has emerged as a promising therapeutic target in cancer. Expression of Wee1 has been associated with poor outcome in certain tumor types, but the prognostic impact and clinical significance in colorectal cancer is unknown. The expression of Wee1 was examined by immunohistochemistry in primary colorectal carcinomas from a prospectively collected patient cohort, and associations with clinicopathological parameters and outcome were investigated. Cell culture experiments were performed using the cell lines RKO and SW620, and the relationship with the metastasis-promoting protein S100A4 was investigated. Nuclear expression was detected in 229 of the 258 tumors analyzed (89 %). Wee1 staining was associated with low pT stage, but no other significant associations with demographic or histopathological variables were found. Moderate Wee1 staining intensity was a predictor of favorable metastasis-free and overall survival compared to strong intensity and no or weak staining. The fraction of positive cells was not a prognostic factor in the present cohort. Inhibition of Wee1 expression using siRNA or treatment with the Wee1 inhibitor MK-1775 reduced expression of the metastasis-promoting protein S100A4, but no relationship between Wee1 and S100A4 was found in the patient samples. In conclusion, Wee1 is highly expressed in primary colorectal carcinomas, but few relevant associations with clinicopathological parameters or outcome were found. The lack of clinical significance of Wee1 expression could indicate that other tumor types might be better suited for further development of Wee1 inhibitors.
引用
收藏
页码:12133 / 12140
页数:8
相关论文
共 35 条
[1]   Forced Mitotic Entry of S-Phase Cells as a Therapeutic Strategy Induced by Inhibition of WEE1 [J].
Aarts, Marieke ;
Sharpe, Rachel ;
Garcia-Murillas, Isaac ;
Gevensleben, Heidrun ;
Hurd, Melissa S. ;
Shumway, Stuart D. ;
Toniatti, Carlo ;
Ashworth, Alan ;
Turner, Nicholas C. .
CANCER DISCOVERY, 2012, 2 (06) :524-539
[2]   Investigation of the prognostic and predictive value of thymidylate synthase, p53, and Ki-67 in patients with locally advanced colon cancer [J].
Allegra, CJ ;
Parr, AL ;
Wold, LE ;
Mahoney, MR ;
Sargent, DJ ;
Johnston, P ;
Klein, P ;
Behan, K ;
O'Connell, MJ ;
Levitt, R ;
Kugler, JW ;
Tirona, MT ;
Goldberg, RM .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (07) :1735-1743
[3]   Prognostic value of thymidylate synthase, Ki-67, and p53 in patients with Dukes' B and C colon cancer:: A national cancer institute-national surgical adjuvant breast and bowel project collaborative study [J].
Allegra, CJ ;
Paik, S ;
Colangelo, LH ;
Parr, AL ;
Kirsch, I ;
Kim, G ;
Klein, P ;
Johnston, PG ;
Wolmark, N ;
Wieand, HS .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (02) :241-250
[4]  
Backert S, 1999, INT J CANCER, V82, P868, DOI 10.1002/(SICI)1097-0215(19990909)82:6<868::AID-IJC16>3.0.CO
[5]  
2-W
[6]   Cell Cycle Proteins Predict Recurrence in Stage II and III Colon Cancer [J].
Belt, Eric J. Th ;
Brosens, Rebecca P. M. ;
Delis-van Diemen, Pien M. ;
Bril, Herman ;
Tijssen, Marianne ;
van Essen, Dirk F. ;
Heymans, Martijn W. ;
Belien, Jeroen A. M. ;
Stockmann, Hein B. A. C. ;
Meijer, Sybren ;
Meijer, Gerrit A. .
ANNALS OF SURGICAL ONCOLOGY, 2012, 19 :S682-S692
[7]   Asymmetric localization of the CDC25B phosphatase to the mother centrosome during interphase [J].
Boutros, Rose ;
Ducommun, Bernard .
CELL CYCLE, 2008, 7 (03) :401-406
[8]   EMMPRIN is associated with S100A4 and predicts patient outcome in colorectal cancer [J].
Boye, K. ;
Nesland, J. M. ;
Sandstad, B. ;
Haugen, M. Haugland ;
Mlandsmo, G. M. ;
Flatmark, K. .
BRITISH JOURNAL OF CANCER, 2012, 107 (04) :667-674
[9]   Nuclear S100A4 is a novel prognostic marker in colorectal cancer [J].
Boye, Kjetil ;
Nesland, Jahn M. ;
Sandstad, Berit ;
Moelandsmo, Gunhild M. ;
Flatmark, Kjersti .
EUROPEAN JOURNAL OF CANCER, 2010, 46 (16) :2919-2925
[10]   S100A4 and Metastasis A Small Actor Playing Many Roles [J].
Boye, Kjetil ;
Maelandsmo, Gunhild M. .
AMERICAN JOURNAL OF PATHOLOGY, 2010, 176 (02) :528-535