Emerging paradigms and recent progress in targeting ErbB in cancers.

Trends Pharmacol Sci

University of Lille, CNRS, Inserm, CHU Lille, UMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, F-59000 Lille, France. Electronic address:

Published: June 2024

AI Article Synopsis

  • The epidermal growth factor receptor (EGFR) family is important in cancer treatment because they are key players in many types of cancer.
  • Standard therapies like tyrosine kinase inhibitors and monoclonal antibodies improve survival but face challenges due to resistance.
  • New approaches, including inhibitory peptides, bispecific antibodies, and insights into the cell surface interactome of ErbB proteins, are emerging as potential strategies to improve treatment efficacy and overcome resistance.

Article Abstract

The epidermal growth factor receptor (EGFR) family is a class of transmembrane proteins, highly regarded as anticancer targets due to their pivotal role in various malignancies. Standard cancer treatments targeting the ErbB receptors include tyrosine kinase inhibitors (TKIs) and monoclonal antibodies (mAbs). Despite their substantial survival benefits, the achievement of curative outcomes is hindered by acquired resistance. Recent advancements in anti-ErbB approaches, such as inhibitory peptides, nanobodies, targeted-protein degradation strategies, and bispecific antibodies (BsAbs), aim to overcome such resistance. More recently, emerging insights into the cell surface interactome of the ErbB family open new avenues for modulating ErbB signaling by targeting specific domains of ErbB partners. Here, we review recent progress in ErbB targeting and elucidate emerging paradigms that underscore the significance of EGF domain-containing proteins (EDCPs) as new ErbB-targeting pathways.

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Source
http://dx.doi.org/10.1016/j.tips.2024.04.009DOI Listing

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