Spleen tyrosine kinase activity regulates epidermal growth factor receptor signaling pathway in ovarian cancer

Yu Yu1, Yohan Suryo Rahmanto1, Yao-An Shen1

  • 1Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins Medical Institutions, Baltimore, MD 21231, United States of America; Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD 21205, United States of America.

Ebiomedicine
|September 8, 2019
PubMed
Abstract

Insights

Spleen tyrosine kinase (SYK) enhances epidermal growth factor receptor (EGFR) and ERBB2 phosphorylation in ovarian cancer. Targeting both SYK and EGFR may offer new therapeutic strategies for patients with recurrent ovarian carcinomas.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Spleen tyrosine kinase (SYK) is upregulated in recurrent ovarian carcinomas, necessitating novel therapeutic approaches.
  • SYK's substrates and their clinical relevance in ovarian cancer remain largely undefined.
  • This study investigates the role of SYK in modulating receptor tyrosine kinase signaling pathways.

Purpose of the Study:

  • To elucidate the interaction between SYK, EGFR, and ERBB2 in ovarian cancer.
  • To determine the functional consequences of SYK-mediated phosphorylation of EGFR and ERBB2.
  • To explore the therapeutic potential of co-targeting SYK and EGFR/ERBB2.

Main Methods:

  • Immunohistochemistry and immunoblotting to detect SYK and EGFR phosphorylation in ovarian serous carcinomas.
  • Kaplan-Meier analysis and log-rank test to assess survival associations.
  • Modulation of SYK activity using small molecule inhibitors, gene knockout, and inducible systems.
  • RNA-sequencing and phosphoproteomic mass spectrometry to identify SYK-regulated downstream targets.

Main Results:

  • SYK activity enhances EGFR and ERBB2 phosphorylation, reducing sensitivity to lapatinib.
  • EGFR activation, but not SYK-mutant EGFR, confers paclitaxel resistance, a phenotype linked to SYK activity in ovarian cancers.
  • SYK inhibition decreased EGFR substrate phosphorylation in xenografts.
  • SYK knockout cells exhibited attenuated EGFR/ERBB2 transcriptional activity and EGF responsiveness.
  • Increased pSYK levels correlated with pEGFR and poor patient survival in ovarian cancer tissues.

Conclusions:

  • SYK positively modulates the EGFR pathway in ovarian cancer.
  • SYK activity is associated with poor prognosis and confers resistance to standard therapies.
  • Co-targeting SYK and EGFR presents a promising therapeutic strategy for ovarian cancer.

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