IGF2/IGF2R expression in urothelial bladder cancer and its implications for tumor recurrence and prognosis

被引:0
|
作者
Wu, Hanli [1 ]
Li, Yumei [1 ]
Cui, Honghong [1 ]
Wu, Wenbin [1 ]
Yang, Huanrong [1 ]
Yang, Xiaoqing [2 ]
Wang, Yueju [3 ]
Li, Peng [4 ]
机构
[1] Yidu Cent Hosp Weifang City, Dept Nephrol, Weifang, Peoples R China
[2] Shandong Univ, Qianfoshan Hosp, Dept Pathol, Jinan, Peoples R China
[3] Soochow Univ, Affiliated Hosp 1, Suzhou, Peoples R China
[4] Qingdao Univ, Affiliated Yantai Yuhuangding Hosp, Dept Med Oncol, Yantai 264000, Shandong, Peoples R China
关键词
Bladder cancer; IGF2; IGF2R; prognosis; recurrence; MANNOSE 6-PHOSPHATE RECEPTORS; CELL LUNG-CANCER; GROWTH; CARCINOMA; POLYMORPHISMS; ACTIVATION; IGF1R; RISK;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Insulin-like growth factor 2 (IGF2) is a secreted growth factor which has growth-regulating, insulin-like and mitogenic activities. Insulin-like growth factor 2 receptor (IGF2R) is a multifunctional receptor functioning by binding with many ligands such as IGF2, growth factor-beta and pro-cathepsin D, etc. To evaluate the expression and clinical significance of IGF2 and IGF2R in urothelial bladder cancer, 126 cases were collected in validation cohort for detection of IGF2 and IGF2R by immunohistochemistry. Moreover, the correlation of IGF2/IGF2R with clinicopathological factors was evaluated with Chi-square test. The association with recurrence and overall survival rate was analyzed with univariate and multivariate analysis. Consequently, the association between IGF2 and tumor recurrence or prognosis was not observed in our study. However, IGF2R overexpression was demonstrated to be significantly correlated with tumor recurrence (P = 0.006) and prognosis (P = 0.019). High expression of IGF2R was identified as an independent indicator of lower recurrence (P = 0.008) and more favorable prognosis (P = 0.010). In conclusion, IGF2R high expression was significantly associated with lower recurrence and better prognosis, suggesting that IGF2R could be considered as a suppressor of bladder cancer by reducing the recurrence rate and improving survival time.
引用
收藏
页码:881 / 888
页数:8
相关论文
共 50 条
  • [1] OPPOSITE IMPRINTING OF THE MOUSE IGF2 AND IGF2R GENES
    WILLISON, K
    [J]. TRENDS IN GENETICS, 1991, 7 (04) : 107 - 109
  • [2] IN VIVO DEVELOPMENT OF CANINE PARTHENOTES AND THE EXPRESSION PATTERN OF Igf2/Igf2r GENES
    Park, J. E.
    Oh, H. J.
    Kim, M. J.
    Kim, G. A.
    Park, E. J.
    Jang, G.
    Lee, B. C.
    [J]. REPRODUCTION FERTILITY AND DEVELOPMENT, 2011, 23 (01) : 158 - 158
  • [3] Angiogenesis and Expression of IGF2R, IGF2, uPAR, and TGFB in a Rat Obesity Model
    Bayless, David S.
    Sheldon, Ryan D.
    Linden, Melissa A.
    Rector, R. Scott
    Laughlin, M. Harold
    [J]. FASEB JOURNAL, 2016, 30
  • [4] Development of an IGF2 super-antagonist by directed evolution of IGF2R
    Frago, Susana
    Strickland, Madeleine
    Hughes, Jennifer
    Williams, Christopher
    Nicholls, Ryan
    Garner, Lee
    Rezgui, Dellel
    Crump, Matthew P.
    Hassan, A. Bassim
    [J]. MOLECULAR CANCER THERAPEUTICS, 2013, 12 (11)
  • [5] Effects of a novel SNP of IGF2R gene on growth traits and expression rate of IGF2R and IGF2 genes in gluteus medius muscle of Egyptian buffalo
    Abu El-Magd, Mohammed
    Abo-Al-Ela, Haitham G.
    El-Nahas, Abeer
    Saleh, Ayman A.
    Mansour, Ali A.
    [J]. GENE, 2014, 540 (02) : 133 - 139
  • [6] Igf2r improves the survival and transmission ratio of Igf2 transgenic mice
    Pravtcheva, Dimitrina D.
    Wise, Thomas L.
    [J]. MOLECULAR REPRODUCTION AND DEVELOPMENT, 2008, 75 (11) : 1678 - 1687
  • [7] A NOVEL ROLE FOR IGF2/IGF2R SIGNALING IN HOMING OF ENDOTHELIAL PROGENITOR CELLS
    Kwon, Y. -G.
    Maeng, Y. S.
    [J]. ATHEROSCLEROSIS SUPPLEMENTS, 2008, 9 (01) : 14 - 15
  • [8] ABSENCE OF REGULATION BY IMPRINTING OF THE IGF2 AND IGF2R GENES IN THE PREIMPLANTATION MOUSE EMBRYO
    LATHAM, KE
    DOHERTY, AS
    SCOTT, CD
    SCHULTZ, RM
    [J]. DEVELOPMENTAL BIOLOGY, 1994, 163 (02) : 537 - 537
  • [9] Imprint status of M6P/IGF2R and IGF2 in chickens
    Catherine M. Nolan
    J. Keith Killian
    James N. Petitte
    Randy L. Jirtle
    [J]. Development Genes and Evolution, 2001, 211 : 179 - 183
  • [10] Imprint status of M6P/IGF2R and IGF2 in chickens
    Nolan, CM
    Killian, JK
    Petitte, JN
    Jirtle, RL
    [J]. DEVELOPMENT GENES AND EVOLUTION, 2001, 211 (04) : 179 - 183