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Updated: Oct 12, 2025

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
New Insight to Overcome Tumor Resistance: An Overview from Cellular to Clinical Therapies
Giulia Mitola1, Paolo Falvo1, Francesco Bertolini1
1Laboratory of Hematology-Oncology, IEO European Institute of Oncology IRCCS, 16, 20139 Milan, Italy.
Abstract:
Disease relapse caused by drug resistance still represents a major clinical hurdle in cancer treatments. Tumor cells may take advantage of different intracellular and genetic systems attenuating the drug effects. Resistant cells or minimal residual disease (MRD) cells have strong clinical relevance, as they might give rise to secondary tumors when the therapy is concluded. Thus, MRDs are crucial therapeutic targets in order to prevent tumor relapse. Therefore, several groups aim at understanding how MRDs are orginated, characterizing their molecular features, and eradicating them. In this review, we will describe MRD from a genetic, evolutionary, and molecular point of view. Moreover, we will focus on the new in vitro, in vivo, preclinical, and clinical studies that aim at eradicating tumor resistance.
Insights
Minimal residual disease (MRD) cells drive cancer relapse due to drug resistance. Understanding MRD origins and molecular features is key to developing new therapies that eradicate resistant cells and prevent tumor recurrence.
Area of Science:
- Oncology
- Cancer Biology
- Genetics
Background:
- Drug resistance in cancer leads to disease relapse, a significant clinical challenge.
- Tumor cells employ various intracellular and genetic mechanisms to evade drug efficacy.
- Minimal residual disease (MRD) cells are critical as they can initiate secondary tumors post-therapy.
Purpose of the Study:
- To review the genetic, evolutionary, and molecular aspects of minimal residual disease (MRD).
- To highlight current research and therapeutic strategies for eradicating drug-resistant cancer cells.
- To provide insights into preventing tumor relapse by targeting MRD.
Main Methods:
- Literature review of in vitro, in vivo, preclinical, and clinical studies.
- Analysis of genetic and molecular characteristics of resistant cells.
- Exploration of evolutionary dynamics contributing to drug resistance.
Main Results:
- MRD cells represent a significant threat for cancer recurrence.
- Diverse genetic and molecular pathways contribute to the survival of resistant tumor cells.
- Emerging therapeutic approaches are being investigated to eliminate MRD.
Conclusions:
- Targeting MRD is essential for improving long-term cancer treatment outcomes.
- A comprehensive understanding of MRD's origins and features is crucial for effective eradication.
- Continued research into novel therapies is vital to overcome drug resistance and prevent relapse.
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