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Author Spotlight: Tracking Electrochemistry on Single Nanoparticles with Surface-Enhanced Raman Scattering Spectroscopy and Microscopy
Published on: May 12, 2023
Tracing the molecular dynamics of living mitochondria under phototherapy via surface-enhanced Raman scattering
Jing Yue1, Yanting Shen1, Lijia Liang1
1State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, College of Chemistry, Jilin University, Changchun 130012, People's Republic of China. xusp@jlu.edu.cn.
Abstract:
Subcellular mitochondrion has become a target for improving the therapeutic efficiency and reducing side damage to normal cells via a combination of many therapeutic strategies. However, the underlying molecular mechanisms associated with cell death induced by subcellular dysfunction remain unknown or disputed. In this study, we investigated the dynamic molecular changes of living mitochondria upon phototherapy (photothermal therapy plus photodynamic therapy, PTT & PDT) by surface-enhanced Raman scattering spectroscopy (SERS) and intended to disclose the photo-induced cell death route in breast cancer cells (MCF-7) taking into account the mitochondrion. Indocyanine green (ICG), a Food and Drug Administration (FDA)-approved clinic blood-injection near-infrared angiographic contrast agent and a PTT & PDT drug, was used for the evaluation of the phototherapy effect. The results revealed that the content of phenylalanine (Phe) in mitochondria evidently increased during the phototherapy-induced cell death process. Moreover, the phototherapy-induced cell apoptosis was mainly regulated through the DNA structures. We expect that the understanding of mitochondrial molecular stress responses will be helpful for the diagnosis and therapy of cellular processes associated with mitochondria and provide valuable guidance for the further design and development of more effective therapeutic platforms and methods at the sub-cellular level.
Insights
Phototherapy targeting mitochondria in breast cancer cells (MCF-7) increases phenylalanine (Phe) levels and triggers apoptosis, primarily via DNA pathways. This research aids in developing novel subcellular therapeutic strategies.
Area of Science:
- Biomedical Engineering
- Molecular Biology
- Cancer Therapy
Background:
- Mitochondria are key targets for cancer therapy to enhance efficacy and reduce side effects.
- Mechanisms of cell death induced by mitochondrial dysfunction are not fully understood.
Purpose of the Study:
- Investigate dynamic molecular changes in mitochondria during phototherapy (PTT & PDT).
- Elucidate the photo-induced cell death pathway in MCF-7 breast cancer cells involving mitochondria.
Main Methods:
- Utilized surface-enhanced Raman scattering (SERS) spectroscopy to monitor living mitochondria.
- Employed Indocyanine green (ICG) as a phototherapy agent for PTT & PDT.
Main Results:
- Observed a significant increase in phenylalanine (Phe) content within mitochondria during phototherapy-induced cell death.
- Determined that phototherapy-induced apoptosis is predominantly regulated through DNA structures.
Conclusions:
- Understanding mitochondrial stress responses is crucial for diagnosing and treating mitochondrial-related cellular processes.
- Findings provide guidance for designing advanced subcellular therapeutic platforms and methods.
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