Targeting HER (ERBB) signaling in head and neck cancer: An essential update

Jun Zhang1, Nabil F Saba2, Georgia Zhuo Chen2

  • 1Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, 1365-C Clifton Road, NE, Atlanta, GA 30322, USA; Department of Internal Medicine, Division of Hematology, Oncology and Blood & Marrow Transplantation, Holden Comprehensive Cancer Center, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, IA 52242, USA.

Insights

Head and neck cancer (HNC) research is exploring new targeted therapies beyond EGFR. This review updates understanding of human epidermal growth factor receptor (HER) signaling in HNC to overcome treatment resistance.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Head and neck cancer (HNC) is a significant global health concern, ranking as the 6th most common carcinoma.
  • Conventional treatments for HNC often result in suboptimal survival rates and significant toxicities.
  • Targeted therapies, particularly those inhibiting the epidermal growth factor receptor (EGFR), have shown limited success in HNC clinical settings, necessitating novel strategies.

Purpose of the Study:

  • To review the emerging roles of human epidermal growth factor receptor (HER) family members beyond EGFR in HNC.
  • To provide a comprehensive update on HER signaling pathways in HNC, addressing resistance mechanisms.
  • To explore novel therapeutic strategies targeting the HER network in HNC.

Main Methods:

  • Literature review focusing on recent advancements in HER signaling research relevant to HNC.
  • Analysis of EGFR nuclear translocation and receptor spatial regulation.
  • Examination of the interdependence and interactions among different HER family members.

Main Results:

  • EGFR-targeted therapy has yielded suboptimal outcomes in HNC, highlighting the need for alternative approaches.
  • Emerging evidence suggests critical roles for other HER family members in HNC development and progression.
  • Understanding the complex interplay within the HER network is crucial for developing effective treatments.

Conclusions:

  • The HER signaling network in HNC is complex, involving multiple receptor members and regulatory mechanisms.
  • Overcoming resistance to current targeted therapies requires a broader understanding of the entire HER family.
  • Future therapeutic strategies should consider targeting multiple HER members or novel aspects of their signaling pathways to improve HNC outcomes.

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