Expression of WNT-5a and ROR2 correlates with disease severity in osteosarcoma

被引:49
|
作者
Lu, Bei-Ji [1 ,2 ]
Wang, Yun-Qing [2 ]
Wei, Xue-Jie [2 ]
Rong, Liang-Qun [2 ]
Wei, Dong [2 ]
Yan, Chang-Ming [2 ]
Wang, Deng-Jie [2 ]
Sun, Jun-Ying [1 ]
机构
[1] Soochow Univ, Dept Orthoped, Affiliated Hosp 1, Suzhou 215006, Jiangsu, Peoples R China
[2] Xuzhou Med Coll, Affiliated Hosp 2, Dept Orthoped, Xuzhou 221000, Jiangsu, Peoples R China
关键词
osteosarcoma; Wnt-5a; Ror2; immunohistochemistry; clinicopathological parameter; TYROSINE KINASE ROR2; SIGNALING PATHWAY; CANCER; WNT5A; CARCINOMA; ONCOLOGY; SARCOMA;
D O I
10.3892/mmr.2012.772
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma, a common malignancy primarily affecting children, generally has a poor prognosis. Novel diagnostic, prognostic and therapeutic markers are required to ameliorate the negative outcomes of this disease. We investigated two potential markers, WNT-5a and ROR2, which are hypothesized to dysregulate WNT signaling pathways to promote tumorigenesis in other types of cancer. We investigated WNT-5a and ROR2 expression using immunohistochemistry in 42 osteosarcoma and 12 osteochondroma specimens, and compared the expression of these proteins with one another as well as with clinicopathological parameters. WNT-5a was detected in 34/42 (81.0%) cases and ROR2 was detected in 31/42 (73.8%) cases, significantly higher than in osteochondroma (16.7 and 25.0%, respectively; both P<0.05). Expression of these proteins was positively correlated (r=0.552, P<0.05). Furthermore, expression of WNT-5a and ROR2 was both correlated with Enneking surgical stage and tumor metastasis (P<0.05), but riot with patient gender, age or pathological type. Thus, WNT-5a and ROR2 were more highly expressed in more severe disease states, and therefore may play a coordinated role in the occurrence and progression of osteosarcoma.
引用
收藏
页码:1033 / 1036
页数:4
相关论文
共 50 条
  • [1] Wnt-5A/Ror2 regulate expression of XPAPC through an alternative noncanonical signaling pathway
    Schambony, Alexandra
    Wedlich, Doris
    DEVELOPMENTAL CELL, 2007, 12 (05) : 779 - 792
  • [2] Dendrobine Regulation Wnt-5a/ROR2 Pathway on Renal Fibrosis in Rats With Ureteral Obstruction
    Huang, Xiaoli
    Wu, Qiang
    Shi, Ju
    Li, Zhifeng
    Liu, Na
    Wu, Yongxian
    LATIN AMERICAN JOURNAL OF PHARMACY, 2023, 42 (12): : 2446 - 2452
  • [3] Autonomous regulation of osteosarcoma cell invasiveness by Wnt5a/Ror2 signaling
    M Enomoto
    S Hayakawa
    S Itsukushima
    D Y Ren
    M Matsuo
    K Tamada
    C Oneyama
    M Okada
    T Takumi
    M Nishita
    Y Minami
    Oncogene, 2009, 28 : 3197 - 3208
  • [4] Prognostic Significance of Ror2 and Wnt5a Expression in Medulloblastoma
    Lee, Seung Eun
    Lim, So Dug
    Kang, So Young
    Suh, Sang Bum
    Suh, Yeon-Lim
    BRAIN PATHOLOGY, 2013, 23 (04) : 445 - 453
  • [5] Autonomous regulation of osteosarcoma cell invasiveness by Wnt5a/Ror2 signaling
    Enomoto, M.
    Hayakawa, S.
    Itsukushima, S.
    Ren, D. Y.
    Matsuo, M.
    Tamada, K.
    Oneyama, C.
    Okada, M.
    Takumi, T.
    Nishita, M.
    Minami, Y.
    ONCOGENE, 2009, 28 (36) : 3197 - 3208
  • [6] ROR2 receptor promotes the migration of osteosarcoma cells in response to Wnt5a
    Dai, Bin
    Yan, Ting
    Zhang, Ailiang
    CANCER CELL INTERNATIONAL, 2017, 17
  • [7] Wnt5a, Ryk and Ror2 expression in glioblastoma subgroups
    Kim, Yuil
    Hong, Mineui
    Do, In-Gu
    Ha, Sang Yun
    Lee, Dakeun
    Suh, Yeon-Lim
    PATHOLOGY RESEARCH AND PRACTICE, 2015, 211 (12) : 963 - 972
  • [8] ROR2 receptor promotes the migration of osteosarcoma cells in response to Wnt5a
    Bin Dai
    Ting Yan
    Ailiang Zhang
    Cancer Cell International, 17
  • [9] Wnt5a, Ryk and Ror2 Expression in Glioblastoma Subgroups
    Suh, Yeon-Lim
    Kim, Yuil
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2015, 74 (06): : 637 - 637
  • [10] Wnt5a and Ror2 expression associate with the disease progress of primary thyroid lymphoma
    Wang, Lei
    Yang, Dong
    Wang, Ying-Hou
    Li, Xi
    Gao, Hong-Ming
    Lv, Jun-Yuan
    Wang, Lei
    Xin, Shi-Jie
    TUMOR BIOLOGY, 2016, 37 (05) : 6085 - 6090