Transcriptomic analysis of mechanism of melanoma cell death induced by photothermal therapy

Guorong Yan1, Lei Shi1, Fuhe Zhang1

  • 1Institute of Photomedicine, Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai, China.

Insights

Photothermal therapy (PTT) effectively treats melanoma by altering gene expression and immune cell composition. This study reveals PTT

Area of Science:

  • Oncology
  • Immunology
  • Biotechnology

Background:

  • Melanoma incidence is increasing, posing significant health and economic burdens.
  • Photothermal therapy (PTT) is a promising local treatment for cutaneous carcinoma, including melanoma.
  • Understanding PTT's mechanism of action is crucial for optimizing its therapeutic efficacy.

Purpose of the Study:

  • To investigate the molecular mechanisms of tumor cell death induced by PTT in melanoma.
  • To analyze gene expression changes and immune cell composition alterations following PTT treatment.
  • To elucidate the transcriptional pathways involved in PTT-mediated melanoma cell death.

Main Methods:

  • B16-F10 melanoma tumor model.
  • Photothermal therapy (PTT) treatment.
  • Differential gene expression analysis (RNA sequencing).
  • Bioinformatic functional annotation of differentially expressed genes (DEGs).
  • Inference of immune cell composition changes.

Main Results:

  • 256 differentially expressed genes (DEGs) identified: 215 downregulated, 41 upregulated by PTT.
  • Functional annotation revealed DEGs predominantly involved in immune and inflammatory responses.
  • PTT treatment altered the composition of immune cells, including regulatory T cells, M2 macrophages, and B cells.
  • Non-invasive PTT treatment triggered melanoma cell death without exogenous photosensitizers.

Conclusions:

  • PTT induces melanoma cell death through significant alterations in gene expression, particularly those related to immune and inflammatory processes.
  • The study provides insights into the transcriptional landscape and immune microenvironment modulation by PTT.
  • These findings contribute to understanding the mechanisms of non-invasive PTT for melanoma treatment.