Combinatorial Therapy of Cancer: Possible Advantages of Involving Modulators of Ionic Mechanisms
1Department of Life Sciences, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Abstract:
Cancer is a global health problem that 1 in 2-3 people can expect to experience during their lifetime. Several different modalities exist for cancer management, but all of these suffer from significant shortcomings in both diagnosis and therapy. Apart from developing completely new therapies, a viable way forward is to improve the efficacy of the existing modalities. One way is to combine these with each other or with other complementary approaches. An emerging latter approach is derived from ionic mechanisms, mainly ion channels and exchangers. We evaluate the evidence for this systematically for the main treatment methods: surgery, chemotherapy, radiotherapy and targeted therapies (including monoclonal antibodies, steroid hormones, tyrosine kinase inhibitors and immunotherapy). In surgery, the possible systemic use of local anesthetics to suppress subsequent relapse is still being discussed. For all the other methods, there is significant positive evidence for several cancers and a range of modulators of ionic mechanisms. This applies also to some of the undesirable side effects of the treatments. In chemotherapy, for example, there is evidence for co-treatment with modulators of the potassium channel (Kv11.1), pH regulation (sodium-hydrogen exchanger) and Na+-K+-ATPase (digoxin). Voltage-gated sodium channels, shown previously to promote metastasis, appear to be particularly useful for co-targeting with inhibitors of tyrosine kinases, especially epidermal growth factor. It is concluded that combining current orthodox treatment modalities with modulators of ionic mechanisms can produce beneficial effects including (i) making the treatment more effective, e.g., by lowering doses; (ii) avoiding the onset of resistance to therapy; (iii) reducing undesirable side effects. However, in many cases, prospective clinical trials are needed to put the findings firmly into clinical context.
Insights
Combining cancer treatments with ion channel modulators shows promise for improving efficacy and reducing side effects. Further clinical trials are needed to confirm these benefits for various cancers.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cancer affects a significant portion of the global population, with current treatments having limitations.
- Improving the efficacy of existing cancer therapies is crucial.
- Ionic mechanisms, particularly ion channels and exchangers, represent an emerging area for therapeutic enhancement.
Purpose of the Study:
- To systematically evaluate the evidence for combining ion mechanism modulators with standard cancer treatments.
- To assess the impact on treatment efficacy, resistance, and side effects across various cancer modalities.
Main Methods:
- Systematic review of evidence for combining ion channel modulators with surgery, chemotherapy, radiotherapy, and targeted therapies.
- Analysis of studies on modulators of potassium channels (Kv11.1), pH regulation (sodium-hydrogen exchanger), Na+-K+-ATPase, and voltage-gated sodium channels.
- Evaluation of co-targeting strategies, such as voltage-gated sodium channels with tyrosine kinase inhibitors.
Main Results:
- Positive evidence exists for combining ion modulators with chemotherapy, radiotherapy, and targeted therapies for several cancers.
- Specific examples include Kv11.1 modulators, sodium-hydrogen exchangers, Na+-K+-ATPase (digoxin), and voltage-gated sodium channels.
- Combinations can enhance treatment effectiveness, overcome resistance, and mitigate adverse effects.
Conclusions:
- Integrating modulators of ionic mechanisms with conventional cancer therapies offers significant potential benefits.
- These benefits include increased treatment effectiveness, prevention of resistance, and reduced side effects.
- Prospective clinical trials are necessary to validate these findings and establish clinical relevance.
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