Targeting Trop2 in solid tumors: a look into structures and novel epitopes

Xinlin Liu1,2, Jiyixuan Li1,2, Junwen Deng1,2

  • 1The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.

Frontiers in Immunology
|January 5, 2024
PubMed

Insights

Trophoblast cell surface antigen 2 (Trop2) is overexpressed in tumors, making it a target for antibody-drug conjugates (ADCs). This review explores Trop2 structure and epitopes to improve targeted cancer therapies.

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Trophoblast cell surface antigen 2 (Trop2) is highly expressed in various solid tumors but minimally in normal tissues.
  • Anti-Trop2 antibody-drug conjugates (ADCs) show efficacy in breast cancer, validating Trop2 as a therapeutic target.
  • Current ADCs face challenges with toxicity and response rates, necessitating improved therapeutic strategies for Trop2-positive cancers.

Purpose of the Study:

  • To review recent advances in understanding Trop2's structure and dynamic attributes.
  • To provide an overview of epitope characteristics for Trop2-targeted agents.
  • To discuss the relationship between anti-Trop2 agent epitopes and their therapeutic functions, efficacy, and specificity.

Main Methods:

  • Literature review of recent advancements in Trop2 research.
  • Analysis of structural attributes and oligomeric assembly of Trop2.
  • Examination of epitope characteristics of existing Trop2-targeted agents.

Main Results:

  • Trop2's complex structure and oligomeric assembly present challenges for targeted therapies.
  • Understanding Trop2 epitopes is crucial for developing effective and specific anti-Trop2 agents.
  • The correlation between epitopes and agent function highlights potential for optimizing targeted therapy efficacy.

Conclusions:

  • Trop2 remains a promising target for cancer therapy, particularly in Trop2-positive cancers.
  • Further research into Trop2's structural dynamics and epitope mapping is essential for advancing targeted therapeutics.
  • Optimizing anti-Trop2 agents based on epitope characteristics can potentially overcome current limitations in efficacy and toxicity.

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