Nanotechnology Approaches for Prevention and Treatment of Chemotherapy‐Induced Neurotoxicity, Neuropathy, and Cardiomyopathy in Breast and Ovarian Cancer Survivors

Ki‐Bum Lee · 2023-04-14

Abstract

Nanotechnology has emerged as a promising approach for the targeted delivery of therapeutic agents while improving their efficacy and safety. As a result, nanomaterial development for the selective targeting of cancers, with the possibility of treating off‐target, detrimental sequelae caused by chemotherapy, is an important area of research. Breast and ovarian cancer are among the most common cancer types in women, and chemotherapy is an essential treatment modality for these diseases. However, chemotherapy‐induced neurotoxicity, neuropathy, and cardiomyopathy are common side effects that can affect breast and ovarian cancer survivors quality of life. Therefore, there is an urgent need to develop effective prevention and treatment strategies for these adverse effects. Nanoparticles (NPs) have extreme potential for enhancing therapeutic efficacy but require continued research to elucidate beneficial interventions for women cancer survivors. In short, nanotechnology‐based approaches have emerged as promising strategies for preventing and treating chemotherapy‐induced neurotoxicity, neuropathy, and cardiomyopathy. NP‐based drug delivery systems and therapeutics have shown potential for reducing the side effects of chemotherapeutics while improving drug efficacy. In this article, the latest nanotechnology approaches and their potential for the prevention and treatment of chemotherapy‐induced neurotoxicity, neuropathy, and cardiomyopathy in breast and ovarian cancer survivors are discussed.

Journal
Small
Funding
New Jersey Commission on Spinal Cord Research Grant CSCR16ERG019NHLBI NIH HHS Grant NHLBIA Bio-Inspired Artificial Transcription Factor for Regeneration of Functional Hair CellsRutgers Biotechnology Training ProgramPQ#12; Targeting Nampt-mediated NAD+ metabolism in chemobrainRutgers Optimizes Innovation (ROI) ProgramNanoparticle-based synthetic transcription factor to induce stem cell myogenesisSan Diego Leading the Advancement of Underrepresented Neuroscientists for Change (LAUNCH) ProgramNanoparticle-based synthetic transcription factor to induce stem cell myogenesisPQ#12; Targeting Nampt-mediated NAD+ metabolism in chemobrainA Bio-Inspired Artificial Transcription Factor for Regeneration of Functional Hair CellsRutgers Biotechnology Training ProgramNSF Grant CBET-1803517Macromolecular Crystallography at the National Synchrotron Light SourceNew Jersey Commission on Spinal Cord Research Grant CSCR17IRG010[Jang R01AG058560 transfer] Role of BubR1 as a juvenile protective factor in hippocampal agingA Bio-Inspired Artificial Transcription Factor for Regeneration of Functional Hair CellsAlzheimer's Association Grant AARG-NTF-21-847862Rutgers Optimizes Innovation (ROI) ProgramA Bio-Inspired Artificial Transcription Factor for Regeneration of Functional Hair CellsN.J. Commission on Cancer Research Grant COCR23PPR007National Science Foundation Grant CBET‐1803517Alzheimer's Association Grant AARG‐NTF‐21‐847862National Heart, Lung, and Blood Institute Grant NHLBIRutgers Optimizes Innovation (ROI) ProgramPQ#12; Targeting Nampt-mediated NAD+ metabolism in chemobrain

NIH R01

3R01DC016612-01S1

NIGMS NIH HHS

T32 GM135141

NCI NIH HHS

R01 CA242158

NHLBI NIH HHS

U01HL150852

NIAMS NIH HHS

R21 AR071101

NINDS NIH HHS

R25 NS117367

NIH R21

R21AR071101

NIH HHS

R01CA242158

NIH R01

5R01DC016612-02S1

NIH T32 Biotechnology Training Program

GM135141

NCRR NIH HHS

P41 RR012408

NIA NIH HHS

R01 AG058560

NIDCD NIH HHS

R01 DC016612

NHLBI NIH HHS

U01 HL150852

NIH R01

1R01DC016612

National Heart, Lung, and Blood Institute

U01HL150852

National Institutes of Health

R01CA242158