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EGFR phosphorylates and inhibits lung tumor suppressor GPRC5A in lung cancer

  • Xiaofeng Lin
  • , Shuangshuang Zhong
  • , Xiaofeng Ye
  • , Yueling Liao
  • , Feng Yao
  • , Xiaohua Yang
  • , Beibei Sun
  • , Jie Zhang
  • , Qi Li
  • , Yong Gao
  • , Yifan Wang
  • , Jingyi Liu
  • , Baohui Han
  • , Y. Baohui Chin
  • , Binhua P. Zhou
  • , Jiong Deng

Producción científica: Articlerevisión exhaustiva

27 Citas (Scopus)

Resumen

Background: GPRC5A is a retinoic acid inducible gene that is preferentially expressed in lung tissue. Gprc5a- knockout mice develop spontaneous lung cancer, indicating Gprc5a is a lung tumor suppressor gene. GPRC5A expression is frequently suppressed in majority of non-small cell lung cancers (NSCLCs), however, elevated GPRC5A is still observed in a small portion of NSCLC cell lines and tumors, suggesting that the tumor suppressive function of GPRC5A is inhibited in these tumors by an unknown mechanism. Methods: In this study, we examined EGF receptor (EGFR)-mediated interaction and tyrosine phosphorylation of GPRC5A by immunoprecipitation (IP)-Westernblot. Tyrosine phosphorylation of GPRC5A by EGFR was systematically identified by site-directed mutagenesis. Cell proliferation, migration, and anchorage-independent growth of NSCLC cell lines stably transfected with wild-type GPRC5A and mutants defective in tyrosine phosphorylation were assayed. Immunohistochemical (IHC) staining analysis with specific antibodies was performed to measure the total and phosphorylated GPRC5A in both normal lung and lung tumor tissues. Result: We found that EGFR interacted with GPRC5A and phosphorylated it in two conserved double-tyrosine motifs, Y317/Y320 and Y347/ Y1, at the C-terminal tail of GPRC5A. EGF induced phosphorylation of GPRC5A, which disrupted GPRC5A-mediated suppression on anchorage-independent growth of NSCLC cells. On contrary, GPRC5A-4 F, in which the four tyrosine residues have been replaced with phenylalanine, was resistant to EGF-induced phosphorylation and maintained tumor suppressive activities. Importantly, IHC analysis with anti-Y317/Y320-P sites showed that GPRC5A was non-phosphorylated in normal lung tissue whereas it was highly tyrosine-phosphorylated in NSCLC tissues. Conclusion: GPRC5A can be inactivated by receptor tyrosine kinase via tyrosine phosphorylation. Thus, targeting EGFR can restore the tumor suppressive functions of GPRC5A in lung cancer.

Idioma originalEnglish
Número de artículo233
PublicaciónMolecular Cancer
Volumen13
N.º1
DOI
EstadoPublished - oct 14 2014

Nota bibliográfica

Publisher Copyright:
© 2014 Lin et al.; licensee BioMed Central Ltd.

Financiación

This work was supported by grants from, Ministry of Science and Technology No. 2011CB504300 (J.Deng) and 2013CB910900 (J.Deng and E.Y.Chin), National Nature Science Foundation of China 91129303 (J.Deng), 81071923 (J.Deng), 81201840 (F.Yao), 81272714 (Q.Li), National Key Basic Research 973 Program of China (2013CB910901) (J.Deng), and Science and Technology Commission of Shanghai (10140902100) (J.Deng). This work was also supported by grants from NIH (2RO1CA125454), Susan G Komen Foundation (KG081310), Mary Kay Ash Foundation (to B.P. Zhou).

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)2RO1CA125454
Mary Kay Ash Foundation
Susan G Komen FoundationKG081310
National Natural Science Foundation of China (NSFC)81071923, 81272714, 81201840, 91129303
Science and Technology Commission of Shanghai Municipality10140902100
Ministry of Science and Technology, Taiwan2011CB504300, 2013CB910900
National Key Research and Development Program of China2013CB910901

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Molecular Medicine
    • Oncology
    • Cancer Research

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