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Published on: January 19, 2019
Synergistic combinations of signaling pathway inhibitors: mechanisms for improved cancer therapy
Paul Dent1, David T Curiel, Paul B Fisher
1Department of Biochemistry and Molecular Biology, Virginia Commonwealth University, School of Medicine, 401 College St., Richmond, VA 23298, USA. pdent@vcu.edu
Abstract:
Cancer cells contain multiple signal transduction pathways whose activities are frequently elevated due to their transformation, and that are often activated following exposure to established cytotoxic therapies including ionizing radiation and chemical DNA damaging agents. Many pathways activated in response to transformation or toxic stresses promote cell growth and invasion and counteract the processes of cell death. As a result of these findings many drugs, predominantly protein and lipid kinase inhibitors, of varying specificities, have been developed to block signaling by cell survival pathways in the hope of killing tumor cells and sensitizing them to toxic therapies. Unfortunately, due to the plasticity of signaling processes within a tumor cell, inhibition of any one growth factor receptor or signaling pathway frequently has only modest long-term effects on cancer cell viability, tumor growth, and patient survival. As a result of this realization, a greater emphasis has begun to be placed on rational combinations of drugs that simultaneously inhibit multiple inter-linked signal transduction/survival pathways. This, it is hoped, will limit the ability of tumor cells to adapt and survive because the activity within multiple parallel survival signaling pathways has been reduced. This review will discuss some of the approaches that have been taken to combine signal transduction modulatory agents to achieve enhanced tumor cell killing.
Insights
Cancer cells activate survival pathways, often resisting single-drug treatments. Combining drugs to inhibit multiple pathways simultaneously offers a promising strategy for enhanced tumor cell killing and improved cancer therapy.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Cancer cells exhibit elevated signal transduction pathways crucial for survival and proliferation.
- These pathways are often activated by cytotoxic therapies, promoting resistance to treatment.
- Existing therapies targeting single pathways show limited long-term efficacy due to cancer cell adaptability.
Purpose of the Study:
- To review strategies for combining signal transduction modulatory agents in cancer therapy.
- To explore approaches that simultaneously inhibit multiple, inter-linked survival pathways.
- To enhance tumor cell killing and overcome therapeutic resistance.
Main Methods:
- Review of current literature on signal transduction pathways in cancer.
- Analysis of drug development focusing on kinase inhibitors.
- Examination of combination therapy approaches targeting multiple pathways.
Main Results:
- Single-target inhibition often leads to modest effects due to pathway plasticity.
- Simultaneous inhibition of multiple pathways can limit tumor cell adaptation and survival.
- Combination therapies aim to create synergistic effects for enhanced tumor cell killing.
Conclusions:
- Combination therapy represents a rational approach to overcome cancer cell resistance.
- Targeting multiple signal transduction pathways simultaneously is crucial for effective cancer treatment.
- Further research into rational drug combinations holds promise for improving patient outcomes.
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