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Article Open Access

LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling

Corrigendum in: /10.3892/ijo.2019.4769
Corrigendum in: /10.3892/ijo.2022.5305
  • Authors:
    • Qungen Xiao
    • Minhai Dong
    • Fangling Cheng
    • Feng Mao
    • Weifeng Zong
    • Kang Wu
    • Heping Wang
    • Ruifan Xie
    • Baofeng Wang
    • Ting Lei
    • Dongsheng Guo
  • View Affiliations / Copyright

    Affiliations: Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, P.R. China
    Copyright: © Xiao et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 1069-1082
    |
    Published online on: July 16, 2018
       https://doi.org/10.3892/ijo.2018.4482
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Abstract

The leucine‑rich repeats and immunoglobulin‑like domains (LRIG) gene family, comprising LRIG1, 2 and 3, encodes integral membrane proteins. It has been well established that LRIG1 negatively regulates multiple growth factor signaling pathways and is considered to be a tumor suppressor; however, the biological functions of LRIG2 remain largely unexplored. It was previously demonstrated that LRIG2 positively regulates epidermal growth factor receptor (EGFR) signaling, the most common aberrant receptor tyrosine kinase (RTK) signaling in glioblastoma multiforme (GBM), which promotes GBM growth. In the present study, the effect of LRIG2 on the proliferation of GBM cells was further addressed, as well as the possible mechanisms underlying the regulatory effect of LRIG2 on platelet‑derived growth factor receptor β (PDGFRβ) signaling, another common oncogenic RTK signaling pathway in GBM. First, the expression levels of endogenous LRIG2 and PDGFRβ were found to vary notably in human GBM, and the LRIG2 expression level was positively correlated with the expression level of PDGFRβ. Furthermore, to the best of our knowledge, this is the first study to demonstrate that LRIG2 promoted the PDGF‑BB‑induced proliferation of GBM cells in vitro and in vivo through regulating the PDGFRβ signaling‑mediated cell cycle progression. Mechanistically, LRIG2 has the ability to physically interact with PDGFRβ, promoting the total expression and the activation of PDGFRβ, and enhancing its downstream signaling pathways of Akt and signal transducer and activator of transcription 3 and the effectors of key regulators of cell cycle progression, resulting in increased GBM cell proliferation. Collectively, these data indicated that LRIG2 may serve as a tumor promoter gene in gliomagenesis by positively regulating PDGFRβ signaling, another important oncogenic RTK signaling pathway, in addition to the previously reported EGFR signaling in GBM modulated by LRIG2, and validated LRIG2 as a promising therapeutic target for the treatment of GBM characterized by multiple aberrant RTK signaling.
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Copy and paste a formatted citation
Spandidos Publications style
Xiao Q, Dong M, Cheng F, Mao F, Zong W, Wu K, Wang H, Xie R, Wang B, Lei T, Lei T, et al: LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305. Int J Oncol 53: 1069-1082, 2018.
APA
Xiao, Q., Dong, M., Cheng, F., Mao, F., Zong, W., Wu, K. ... Guo, D. (2018). LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305. International Journal of Oncology, 53, 1069-1082. https://doi.org/10.3892/ijo.2018.4482
MLA
Xiao, Q., Dong, M., Cheng, F., Mao, F., Zong, W., Wu, K., Wang, H., Xie, R., Wang, B., Lei, T., Guo, D."LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305". International Journal of Oncology 53.3 (2018): 1069-1082.
Chicago
Xiao, Q., Dong, M., Cheng, F., Mao, F., Zong, W., Wu, K., Wang, H., Xie, R., Wang, B., Lei, T., Guo, D."LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305". International Journal of Oncology 53, no. 3 (2018): 1069-1082. https://doi.org/10.3892/ijo.2018.4482
Copy and paste a formatted citation
x
Spandidos Publications style
Xiao Q, Dong M, Cheng F, Mao F, Zong W, Wu K, Wang H, Xie R, Wang B, Lei T, Lei T, et al: LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305. Int J Oncol 53: 1069-1082, 2018.
APA
Xiao, Q., Dong, M., Cheng, F., Mao, F., Zong, W., Wu, K. ... Guo, D. (2018). LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305. International Journal of Oncology, 53, 1069-1082. https://doi.org/10.3892/ijo.2018.4482
MLA
Xiao, Q., Dong, M., Cheng, F., Mao, F., Zong, W., Wu, K., Wang, H., Xie, R., Wang, B., Lei, T., Guo, D."LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305". International Journal of Oncology 53.3 (2018): 1069-1082.
Chicago
Xiao, Q., Dong, M., Cheng, F., Mao, F., Zong, W., Wu, K., Wang, H., Xie, R., Wang, B., Lei, T., Guo, D."LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling Corrigendum in /10.3892/ijo.2019.4769 Corrigendum in /10.3892/ijo.2022.5305". International Journal of Oncology 53, no. 3 (2018): 1069-1082. https://doi.org/10.3892/ijo.2018.4482
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