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TREX1 Inactivation Unleashes Cancer Cell STING-Interferon Signaling and Promotes Antitumor Immunity
Tetsuo Tani1, Haritha Mathsyaraja2, Marco Campisi1
1Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Abstract:
A substantial fraction of cancers evade immune detection by silencing Stimulator of Interferon Genes (STING)-Interferon (IFN) signaling. Therapeutic reactivation of this program via STING agonists, epigenetic, or DNA-damaging therapies can restore antitumor immunity in multiple preclinical models. Here we show that adaptive induction of three prime exonuclease 1 (TREX1) restrains STING-dependent nucleic acid sensing in cancer cells via its catalytic function in degrading cytosolic DNA. Cancer cell TREX1 expression is coordinately induced with STING by autocrine IFN and downstream STAT1, preventing signal amplification. TREX1 inactivation in cancer cells thus unleashes STING-IFN signaling, recruiting T and natural killer (NK) cells, sensitizing to NK cell-derived IFNγ, and cooperating with programmed cell death protein 1 blockade in multiple mouse tumor models to enhance immunogenicity. Targeting TREX1 may represent a complementary strategy to induce cytosolic DNA and amplify cancer cell STING-IFN signaling as a means to sensitize tumors to immune checkpoint blockade (ICB) and/or cell therapies.
Significance:
STING-IFN signaling in cancer cells promotes tumor cell immunogenicity. Inactivation of the DNA exonuclease TREX1, which is adaptively upregulated to limit pathway activation in cancer cells, recruits immune effector cells and primes NK cell-mediated killing. Targeting TREX1 has substantial therapeutic potential to amplify cancer cell immunogenicity and overcome ICB resistance. This article is featured in Selected Articles from This Issue, p. 695.
Insights
Inactivating TREX1 enzyme in cancer cells unleashes STING-IFN signaling, enhancing antitumor immunity. This approach sensitizes tumors to immune checkpoint blockade and cell therapies by boosting immunogenicity.
Area of Science:
- Immunology
- Cancer Biology
- Molecular Oncology
Background:
- Cancers often evade immune detection by suppressing Stimulator of Interferon Genes (STING)-Interferon (IFN) signaling.
- Therapeutic strategies like STING agonists and epigenetic modifiers can restore antitumor immunity in preclinical cancer models.
Purpose of the Study:
- To investigate the role of three prime exonuclease 1 (TREX1) in regulating STING-IFN signaling within cancer cells.
- To explore the potential of targeting TREX1 to enhance cancer cell immunogenicity and therapeutic responses.
Main Methods:
- Assessed TREX1 expression and its correlation with STING-IFN signaling in cancer cells.
- Utilized TREX1 inactivation in preclinical mouse tumor models.
- Evaluated the impact of TREX1 targeting on immune cell recruitment, NK cell activity, and response to immune checkpoint blockade (ICB).
Main Results:
- Adaptive induction of TREX1 restrains STING-dependent nucleic acid sensing by degrading cytosolic DNA.
- TREX1 expression is upregulated by autocrine IFN and STAT1, preventing STING-IFN signal amplification.
- TREX1 inactivation in cancer cells activates STING-IFN signaling, recruiting T and NK cells, and enhancing sensitivity to IFNγ and ICB.
Conclusions:
- Targeting TREX1 can amplify cancer cell STING-IFN signaling, increasing tumor immunogenicity.
- TREX1 inactivation represents a complementary strategy to sensitize tumors to ICB and cell therapies.
- Modulating TREX1 offers a novel therapeutic avenue for overcoming immune evasion in cancer.
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