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.

The Analyst
|August 10, 2019
PubMed

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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