When ‘Dirty’ Drugs Become Useful: Peptide-Guided Exposure Engineering for the Repurposing of Cancer Drugs
Serena Marchiò

TL;DR
This paper proposes using peptides to improve the effectiveness of repurposed cancer drugs by controlling where and when they act in tumors.
Contribution
The paper introduces peptide-guided exposure engineering as a novel strategy for drug repurposing in oncology.
Findings
Peptides can enhance tumor accessibility and reduce systemic toxicity of repurposed drugs.
Exposure control via peptides allows for spatial and temporal targeting of pharmacological activity.
An exposure-centric screening workflow is proposed to prioritize repurposed agents for peptide-guided rescue.
Abstract
Drug repurposing in oncology is often framed as a drug–target matching exercise, yet many candidates with plausible biological rationales fail in the clinic. In solid tumors, therapeutic outcomes are constrained not only by pharmacological target relevance but also by limited tumor accessibility, heterogeneous intratumoral exposure, loss of context-dependent activity, and dose-limiting systemic toxicity. This perspective argues that repurposing strategies should treat exposure engineering as a design principle alongside molecular selectivity. Peptides that bind cell- or matrix-associated molecules at the tumor site have the potential to implement spatial, temporal, and subcellular control over where and when a drug engages its pharmacological target, thereby enabling confinement of polypharmacology to tumor contexts. Mechanistic modes of peptide-enabled exposure selectivity (homing,…
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Taxonomy
TopicsClick Chemistry and Applications · Cancer Cells and Metastasis · Protein Degradation and Inhibitors
