1. Academic Validation
  2. Clinical applications of STING agonists in cancer immunotherapy: current progress and future prospects

Clinical applications of STING agonists in cancer immunotherapy: current progress and future prospects

  • Front Immunol. 2024 Oct 2:15:1485546. doi: 10.3389/fimmu.2024.1485546.
Bin Wang # 1 Wanpeng Yu # 1 Hongfei Jiang 1 2 Xiangwei Meng 3 Dongmei Tang 1 4 Dan Liu 2
Affiliations

Affiliations

  • 1 The Afffliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
  • 2 Medical Education Department, Guangdong Provincial People's Hospital, Zhuhai Hospital (Jinwan Central Hospital of Zhuhai), Zhuhai, China.
  • 3 Department of Drug Clinical Trials, Zibo Central Hospital, Zibo, China.
  • 4 Department of Anesthesia, Affiliated Hospital of Qingdao University, Qingdao, China.
  • # Contributed equally.
Abstract

The STING (Stimulator of Interferon Genes) pathway is pivotal in activating innate immunity, making it a promising target for Cancer Immunotherapy. STING agonists have shown potential in enhancing immune responses, particularly in tumors resistant to traditional therapies. This scholarly review examines the diverse categories of STING agonists, encompassing CDN analogues, non-CDN chemotypes, CDN-infused exosomes, engineered Bacterial vectors, and hybrid structures of small molecules-nucleic acids. We highlight their mechanisms, clinical trial progress, and therapeutic outcomes. While these agents offer significant promise, challenges such as toxicity, tumor heterogeneity, and delivery methods remain obstacles to their broader clinical use. Ongoing research and innovation are essential to overcoming these hurdles. STING agonists could play a transformative role in Cancer treatment, particularly for patients with hard-to-treat malignancies, by harnessing the body's immune system to target and eliminate Cancer cells.

Keywords

STING agonists; cGAS-STING pathway; cancer immunotherapy; innate immunity; tumor microenvironment.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-160406
    99.08%, STING Agonist