NIR-II Imaging-Guided Phototherapy-Induced Senescence Reprograms Immunosuppressive Tumor Microenvironment for Potent

Zifan Yang1, Xinwen Ou2, Zhuomin Tang1,3

  • 1Department of Breast Surgery, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530000, China.

ACS Nano
|June 11, 2026
PubMed

Insights

This study introduces a novel phototherapy approach to induce cellular senescence and enhance anti-tumor immunity in triple-negative breast cancer. The treatment effectively remodels the tumor microenvironment, leading to tumor regression and long-term immune memory.

Area of Science:

  • Oncology
  • Immunology
  • Nanomedicine

Background:

  • Cellular senescence is a key tumor suppressor mechanism involving cell-cycle arrest and regulating the tumor microenvironment (TME).
  • Exploiting senescence inducers to promote senescence-associated secretory phenotypes (SASPs) and enhance immune infiltration is an underexplored strategy.
  • Triple-negative breast cancer (TNBC) presents a highly immunosuppressive TME, necessitating novel therapeutic approaches.

Purpose of the Study:

  • To develop a phototherapy-based strategy for inducing senescence and overcoming the immunosuppressive TME in TNBC.
  • To investigate the potential of a nanoplatform delivering an Aurora kinase inhibitor and a phototheranostic molecule for combined therapy.
  • To evaluate the impact of this approach on SASP expression, immune cell infiltration, and tumor regression.

Main Methods:

  • Development of a reactive oxygen species-responsive nanoplatform co-delivering alisertib (Aurora kinase inhibitor) and a near-infrared emissive molecule.
  • Application of 808 nm laser phototherapy to induce alisertib release, oxidative stress, and cellular senescence.
  • Analysis of SASP secretion, immune cell populations (cytotoxic T lymphocytes, myeloid-derived suppressor cells, regulatory T cells), and tumor growth in a TNBC model.
  • Assessment of immunological memory and systemic toxicity.

Main Results:

  • Phototherapy induced alisertib release and oxidative stress, leading to senescence and SASP secretion.
  • The nanodrug remodeled the TME by activating cytotoxic T lymphocytes and depleting immunosuppressive cells.
  • Efficient tumor regression was achieved, accompanied by the establishment of durable immunological memory.
  • The treatment demonstrated no significant systemic toxicity.

Conclusions:

  • Senescence induction via phototherapy is a promising strategy to overcome immunosuppressive TMEs in TNBC.
  • The developed nanoplatform effectively integrates phototherapy-enhanced drug delivery with SASP-driven immunosurveillance.
  • This approach represents a potential next-generation photoimmunotherapy for cancer treatment.

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