Chromosome 17p13 deletion is associated with an aggressive tumor phenotype in clear cell renal cell carcinoma

被引：0
|
作者：
Till Eichenauer
Navid Shadanpour
Martina Kluth
Cosima Göbel
Sören Weidemann
Christoph Fraune
Franziska Büscheck
Claudia Hube-Magg
Christina Möller-Koop
Roland Dahlem
Margit Fisch
Michael Rink
Silke Riechardt
Eike Burandt
Christian Bernreuther
Sarah Minner
Ronald Simon
Guido Sauter
Waldemar Wilczak
Till Clauditz
机构：
[1] University Medical Center Hamburg-Eppendorf,Institute of Pathology
[2] University Medical Center Hamburg-Eppendorf,Department of Urology
来源：
World Journal of Surgical Oncology | / 18卷
关键词：
Renal cell cancer; 17p13 deletion; Fluorescence in situ hybridization; Tissue microarray; Prognosis;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [1] Chromosome 17p13 deletion is associated with an aggressive tumor phenotype in clear cell renal cell carcinoma
    Eichenauer, Till
    Shadanpour, Navid
    Kluth, Martina
    Goebel, Cosima
    Weidemann, Soeren
    Fraune, Christoph
    Buescheck, Franziska
    Hube-Magg, Claudia
    Moeller-Koop, Christina
    Dahlem, Roland
    Fisch, Margit
    Rink, Michael
    Riechardt, Silke
    Burandt, Eike
    Bernreuther, Christian
    Minner, Sarah
    Simon, Ronald
    Sauter, Guido
    Wilczak, Waldemar
    Clauditz, Till
    WORLD JOURNAL OF SURGICAL ONCOLOGY, 2020, 18 (01)
  • [2] Chromosome 9p Deletions Identify an Aggressive Phenotype of Clear Cell Renal Cell Carcinoma
    La Rochelle, Jeffrey
    Klatte, Tobias
    Dastane, Aditi
    Rao, Nagesh
    Seligson, David
    Said, Jonathan
    Shuch, Brian
    Zomorodian, Nazy
    Kabbinavar, Fairooz
    Belldegrun, Arie
    Pantuck, Allan J.
    CANCER, 2010, 116 (20) : 4696 - 4702
  • [3] CHROMOSOME 9P DELETIONS IN CLEAR CELL RENAL CELL CARCINOMA ARE ASSOCIATED WITH AGGRESSIVE DISEASE.
    La Rochelle, Jeffrey C.
    Dastane, Aditi
    Rao, Nagesh
    Klatte, Tobias
    Shuch, Brian
    de Martino, Michela
    Zomorodian, Nazy
    Kabbinavar, Fairooz
    Said, Jonathan W.
    Belldegrun, Arie S.
    Pantuck, Allan J.
    JOURNAL OF UROLOGY, 2009, 181 (04): : 112 - 112
  • [4] PROGNOSTIC ROLE OF CHROMOSOME 9P DELETION IN PATIENTS WITH CLEAR CELL RENAL CELL CARCINOMA
    Ficarra, Vincenzo
    Novara, Giacomo
    Brunelli, Matteo
    Gobbo, Stefano
    Galfano, Antonio
    Cavalleri, Stefano
    Artibani, Walter
    Martignoni, Guido
    JOURNAL OF UROLOGY, 2009, 181 (04): : 354 - 355
  • [5] Prognostic significance of chromosome 9p deletion status in clear cell Renal Cell Carcinoma
    Mokadem, I.
    Fitzpatrick, J.
    Bondad, J.
    Cunningham, J.
    Fleming, S.
    Goodman, C.
    Nabi, G.
    BJU INTERNATIONAL, 2013, 111 : 34 - 35
  • [6] ALLELIC LOSS AT CHROMOSOME-3P CHARACTERIZES CLEAR CELL PHENOTYPE OF RENAL-CELL CARCINOMA
    OGAWA, O
    KAKEHI, Y
    OGAWA, K
    KOSHIBA, M
    SUGIYAMA, T
    YOSHIDA, O
    CANCER RESEARCH, 1991, 51 (03) : 949 - 953
  • [7] NICOTINAMIDE N-METHYLTRANSFERASE OVEREXPRESSION IS ASSOCIATED WITH AN AGGRESSIVE BIOLOGIC PHENOTYPE AND CHEMORESISTANCE IN CLEAR CELL RENAL CELL CARCINOMA
    Stamatakis, Lambros
    Margulis, Vitaly
    Maity, Tapati
    Zhang, Xiu-Ying
    Cooper, Simon J.
    Copland, John A.
    Wood, Christopher G.
    JOURNAL OF UROLOGY, 2009, 181 (04): : 155 - 155
  • [8] Chromosome 9p deletion in clear cell renal cell carcinoma predicts recurrence and survival following surgery
    I El-Mokadem
    J Fitzpatrick
    J Bondad
    P Rauchhaus
    J Cunningham
    N Pratt
    S Fleming
    G Nabi
    British Journal of Cancer, 2014, 111 : 1381 - 1390
  • [9] Chromosome 9p deletion in clear cell renal cell carcinoma predicts recurrence and survival following surgery
    El-Mokadem, I.
    Fitzpatrick, J.
    Bondad, J.
    Rauchhaus, P.
    Cunningham, J.
    Pratt, N.
    Fleming, S.
    Nabi, G.
    BRITISH JOURNAL OF CANCER, 2014, 111 (07) : 1381 - 1390
  • [10] PRENATAL-DIAGNOSIS OF DELETION 17P13 ASSOCIATED WITH DIGEORGE ANOMALY
    GREENBERG, F
    COURTNEY, KB
    WESSELS, RA
    HUHTA, J
    CARPENTER, RJ
    RICH, DC
    LEDBETTER, DH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 31 (01): : 1 - 4
12345