4.7 Article

Statin in combination with cisplatin makes favorable tumor-immune microenvironment for immunotherapy of head and neck squamous cell carcinoma

Journal

CANCER LETTERS
Volume 522, Issue -, Pages 198-210

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2021.09.029

Keywords

Anticancer drug combinations; Cis-diamminedichloroplatinum (II); Head and neck neoplasms; Immunogenic cell death; Hydroxymethylglutaryl-CoA reductase inhibitors

Categories

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT in Korea [2017R1A3B1023418, 2020R1C1C1003539]
  2. National Research Foundation of Korea [2020R1C1C1003539] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study showed that statins can enhance the anticancer effects of cisplatin, activate antigen-presenting cells, and increase tumor-specific CD8(+) T cells, thus potentiating the efficacy of immunotherapy in HNSCC. The combination of statins with anti-PD-1 antibody further led to tumor eradication and improved survival in tumor-bearing mice. This suggests a potential repurposing of statins as an adjuvant immunotherapeutic option for HNSCC.
The purpose of this study was to determine whether statins can enhance anticancer effects in head and neck squamous cell carcinoma (HNSCC) when used with cisplatin and act as immunogenic cell death (ICD) inducers that can be used in cancer immunotherapy. Statins alone showed both in vitro and in vivo inhibitory effects against HNSCC, and synergistic antitumor effects were observed when combined with cisplatin in a syngeneic murine HNSCC model. Statins increased calreticulin exposure and endoplasmic reticulum stress-related signals in HNSCC cells. In addition, it was confirmed that statins could activate antigen-presenting cells and tumor-specific CD8(+) T cells with an increase in their numbers in the tumor tissues and draining lymph nodes, with this effect showing significant improvement following the combination therapy with cisplatin. Moreover, in triple combination with both cisplatin and anti-programmed cell death 1 receptor (anti-PD-1) antibody, statins dramatically induced further tumor eradication and improved the survival of tumor-bearing mice. Taken together, these results demonstrate that statins, administered in combination with anti-PD-1 antibody, could enhance the anticancer effect of cisplatin and potentiate the efficacy of immunotherapy for HNSCC and present a rationale for repurposing statins as an adjuvant immunotherapeutic option for HNSCC.

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