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Monitoring of Nanodrug Accumulation in Murine Breast Cancer Metastases
Published on: August 23, 2024
Bridging molecular insights and clinical application: non-coding RNAs, targeted drug delivery, and metastatic breast
Sohini Chakraborty1,2, Satarupa Banerjee3
1Department of Biotechnology, School of Applied Sciences, Reva University, Bengaluru, 560064, Karnataka, India.
Abstract:
Breast cancer (BC) is one of the most common types of malignancy diagnosed globally. Metastasis plays a major role in most of the cancer-related mortality among affected patients. Despite the advances in the areas of early detection and localized treatment modalities, there prevail several challenges which the therapeutic strategies encounter, like drug resistance, tumor heterogeneity, and drug delivery. This review presents a comprehensive and detailed overview of organ-specific metastasis that occur in BC, specifically emphasizing key sites such as the bone, liver, lung, and brain. It also outlines the significance of various therapies like chemotherapies, endocrine therapies, targeted therapies and immunotherapies that have been clinically approved to date. The review specifically emphasizes the molecular mechanisms by which non-coding RNAs (ncRNAs) act to exert their effects in regulating drug resistance. It also addresses the new advances in nanotechnology-based drug delivery systems (DDS) that function to enhance the specificity of treatments while simultaneously reducing systemic toxicity. Beyond ncRNAs, this review also explores other critical mechanisms of drug resistance in metastatic BC, including efflux transporter activity, target gene mutations, and micro-environmental factors, to mention a few. Moreover, the review also discusses the clinical significance of combination therapies and new therapeutic strategies, including the use of repurposed drugs and the concepts of personalized medicine. A greater understanding of the ncRNA-mediated signaling pathways, in combination with the latest advances in drug delivery systems, has the potential to greatly improve therapeutic efficacy and could result in more favorable clinical outcomes in the treatment of metastatic BC (MBC).
Insights
Metastatic breast cancer (MBC) challenges include drug resistance and delivery. This review covers organ-specific metastasis, therapies, non-coding RNAs (ncRNAs), and nanotechnology for improved treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Nanotechnology
Background:
- Breast cancer (BC) is a leading global malignancy, with metastasis driving mortality.
- Therapeutic challenges in BC include drug resistance, tumor heterogeneity, and drug delivery limitations.
- Understanding organ-specific metastasis (bone, liver, lung, brain) is crucial for effective treatment.
Purpose of the Study:
- To provide a comprehensive overview of organ-specific metastasis in breast cancer.
- To review current and emerging therapeutic strategies, including chemotherapies, targeted therapies, and immunotherapies.
- To highlight the role of non-coding RNAs (ncRNAs) and nanotechnology-based drug delivery systems (DDS) in overcoming drug resistance.
Main Methods:
- Literature review of organ-specific metastasis in breast cancer.
- Analysis of molecular mechanisms underlying drug resistance, including ncRNAs, efflux transporters, and micro-environmental factors.
- Exploration of advancements in nanotechnology-based drug delivery systems (DDS).
Main Results:
- Non-coding RNAs (ncRNAs) significantly regulate drug resistance in metastatic breast cancer (MBC).
- Nanotechnology-based drug delivery systems (DDS) offer enhanced treatment specificity and reduced systemic toxicity.
- Combination therapies, repurposed drugs, and personalized medicine show promise for MBC treatment.
Conclusions:
- Integrating knowledge of ncRNA pathways and advanced DDS can improve therapeutic efficacy in MBC.
- Addressing drug resistance mechanisms is key to improving clinical outcomes for metastatic breast cancer patients.
- Further research into ncRNAs and nanotechnology holds potential for novel MBC treatment strategies.
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