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Quadruple-Checkerboard: A Modification of the Three-Dimensional Checkerboard for Studying Drug Combinations
Published on: July 24, 2021
Multidrug Resistance: Are We Still Afraid of the Big Bad Wolf
Abdulelah Alhazza1,2, Adenike Oyegbesan1, Emira Bousoik3
1Department of Biomedical and Pharmaceutical Sciences, Chapman University School of Pharmacy, Harry and Diane Rinker Health Science Campus, #211, 9401 Jeronimo Road, Irvine, CA 92618, USA.
Abstract:
After the era of multidrug resistance (MDR) against cytotoxic chemotherapy, the development of resistance against newly developed molecularly targeted drugs also seems inevitable. While the mechanisms involved in resistance against these two categories of anticancer drugs are different, the principles are similar: inherent resistance (also known as primary resistance) is a result of heterogeneity in cancer cells where a subpopulation of the cells do not show a favorable initial response to the drug, while acquired resistance (or secondary resistance), as the name suggests, is developed after repeated treatments due to the plasticity of cancer cells. Despite the introduction of a variety of molecularly targeted drugs to clinical practice, chemotherapy is still at the forefront of the battle against cancer. In this manuscript, we review the major mechanisms involved in MDR and resistance against different categories of molecularly targeted drugs separately, and review some of the strategies studied to overcome the resistance against cancer therapy. While MDR mechanisms have been reviewed previously, the molecular mechanisms of resistance to the latest generations of anticancer drugs are rarely reviewed as a group, and the connection between the two categories of resistance is often missing in this type of publication. Our aim is to illustrate a comprehensive picture of what the landscape of cancer treatment is today with respect to resistance. While this picture seems bleak, and it is the common belief that resistance is inevitable, understanding the mechanisms involved could potentially lead to more efficient approaches to overcoming this so far unbeatable obstacle.
Insights
Cancer treatment resistance to chemotherapy and targeted drugs is inevitable due to inherent or acquired mechanisms. Understanding these resistance pathways is key to developing more effective cancer therapies.
Area of Science:
- Oncology
- Cancer Biology
- Pharmacology
Background:
- Multidrug resistance (MDR) to chemotherapy is a long-standing challenge in cancer treatment.
- Emerging resistance to molecularly targeted drugs mirrors principles seen in MDR, posing new therapeutic hurdles.
- Cancer cell heterogeneity and plasticity drive both inherent (primary) and acquired (secondary) resistance.
Purpose of the Study:
- To comprehensively review major mechanisms of MDR against cytotoxic chemotherapy.
- To delineate molecular mechanisms of resistance to various classes of molecularly targeted anticancer drugs.
- To explore strategies for overcoming both MDR and targeted therapy resistance.
Main Methods:
- Literature review of established and emerging resistance mechanisms.
- Separate analysis of resistance pathways for chemotherapy and molecularly targeted agents.
- Synthesis of current understanding and identification of knowledge gaps.
Main Results:
- Detailed review of MDR mechanisms.
- Exploration of diverse resistance pathways to molecularly targeted therapies.
- Identification of strategies to combat treatment resistance.
Conclusions:
- Resistance to cancer therapies, both traditional and targeted, is a complex and evolving challenge.
- A unified understanding of resistance mechanisms is crucial for advancing cancer treatment.
- Further research into resistance pathways may unlock novel therapeutic approaches.
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