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Updated: Dec 14, 2025

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
Challenges and Opportunities in Cancer Drug Resistance
Richard A Ward1, Stephen Fawell2, Nicolas Floc'h3
1Medicinal Chemistry, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, U.K.
Abstract:
There has been huge progress in the discovery of targeted cancer therapies in recent years. However, even for the most successful and impactful cancer drugs which have been approved, both innate and acquired mechanisms of resistance are commonplace. These emerging mechanisms of resistance have been studied intensively, which has enabled drug discovery scientists to learn how it may be possible to overcome such resistance in subsequent generations of treatments. In some cases, novel drug candidates have been able to supersede previously approved agents; in other cases they have been used sequentially or in combinations with existing treatments. This review summarizes the current field in terms of the challenges and opportunities that cancer resistance presents to drug discovery scientists, with a focus on small molecule therapeutics. As part of this review, common themes and approaches have been identified which have been utilized to successfully target emerging mechanisms of resistance. This includes the increase in target potency and selectivity, alternative chemical scaffolds, change of mechanism of action (covalents, PROTACs), increases in blood-brain barrier permeability (BBBP), and the targeting of allosteric pockets. Finally, wider approaches are covered such as monoclonal antibodies (mAbs), bispecific antibodies, antibody drug conjugates (ADCs), and combination therapies.
Insights
Targeted cancer therapies face common resistance. This review explores strategies for overcoming drug resistance, including novel small molecules and antibody-based therapies, to improve patient outcomes.
Area of Science:
- Oncology
- Pharmacology
- Drug Discovery
Background:
- Significant advancements in targeted cancer therapies have been achieved.
- Innate and acquired resistance mechanisms are prevalent, limiting treatment efficacy.
- Understanding resistance is crucial for developing next-generation cancer drugs.
Purpose of the Study:
- To review challenges and opportunities in overcoming cancer drug resistance.
- To focus on strategies for small molecule therapeutics.
- To identify common themes and approaches for targeting resistance mechanisms.
Main Methods:
- Literature review of current research on cancer resistance.
- Analysis of strategies employed to overcome resistance.
- Categorization of therapeutic approaches, including small molecules and biologics.
Main Results:
- Identified key strategies: increased target potency/selectivity, novel scaffolds, altered mechanisms of action (e.g., PROTACs), enhanced blood-brain barrier permeability, and allosteric targeting.
- Highlighted broader approaches: monoclonal antibodies (mAbs), bispecific antibodies, antibody-drug conjugates (ADCs), and combination therapies.
Conclusions:
- Overcoming cancer resistance requires innovative drug discovery approaches.
- A combination of enhanced small molecules and advanced biologics offers promising avenues.
- Continued research into resistance mechanisms is vital for future therapeutic development.
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