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March 15, 2026Cancer Biology and Medicine0 citationsOpen Access

Click chemistry-driven tumor theranostics: recent advances, challenges, and future perspectives

DHDayong HouXLXiangpeng LiNZN. Zhang

Key Points

  • To summarize recent developments in click chemistry applications for tumor theranostics and address current challenges.
  • Overview of core click reactions and biomedical applications.
  • Review of tumor diagnosis methods including molecular imaging probes and circulating tumor cell detection.
  • Discussion of tumor therapy strategies: chemotherapy, phototherapy, immunotherapy, and gene therapy.
  • Examination of integrated theranostics with multimodal imaging-guided combinatorial therapy.
  • Critical analysis of challenges in biocompatibility and in vivo reaction efficiency.
  • Click chemistry enhances the efficiency and selectivity of tumor theranostic systems.
  • Recent advances include stimuli-responsive reactions and AI-assisted probe design.
  • Challenges in biocompatibility and reaction efficiency are identified as critical issues for future research.

Abstract

Tumor theranostics, which integrates accurate diagnosis and precise therapy, has emerged as a pivotal approach in modern oncology for improving treatment efficacy and reducing off-target toxicity. Click chemistry, which is characterized by high efficiency, selectivity, biocompatibility, and modularity, has become an indispensable tool for constructing versatile theranostic systems. This review systematically summarizes the recent progress in click chemistry-based tumor theranostic systems, starting with an overview of core click reactions and the unique features in biomedical applications. We then focus on the application of click chemistry within a diagnosis-therapy-theranostics framework to three key aspects of tumor theranostics: (i) tumor diagnosis (molecular imaging probes and circulating tumor cell detection); (ii) tumor therapy (chemotherapy, phototherapy, immunotherapy, and gene therapy); and (iii) integrated theranostics (multimodal imaging-guided combinatorial therapy). Furthermore, the current challenges, such as the biocompatibility of catalysts and in vivo reaction efficiency, are critically discussed. Finally, we highlight promising directions, including stimuli-responsive click reactions, AI-assisted probe design, and personalized theranostic systems. This review not only serves as a comprehensive reference for researchers but also highlights how click chemistry uniquely bridges molecular design with clinical functionality, distinguishing click chemistry from conventional conjugation or labeling methods by enabling spatiotemporal control, modular integration, and bioorthogonal precision in complex biological settings.

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Cite This Study

Hou et al. (2026) studied this question.

synapsesocial.com/papers/69b64d48b42794e3e660e07bhttps://doi.org/10.20892/j.issn.2095-3941.2025.0667
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