Genetically Engineered Probiotic Limosilactobacillus reuteri Releasing IL-22 (LR-IL-22) Modifies the Tumor Microenvironment, Enabling Irradiation in Ovarian Cancer.
Diala F HamadeMichael W EpperlyRenee FisherWen HouDonna ShieldsJan-Peter van PijkerenBrian J LeibowitzLan G CoffmanHong WangM Saiful HuqZiyu HuangClaude J RogersAnda M VladJoel S GreenbergerAmitava MukherjeePublished in: Cancers (2024)
Despite recent advances in cancer therapy, ovarian cancer remains the most lethal gynecological cancer worldwide, making it crucial and of the utmost importance to establish novel therapeutic strategies. Adjuvant radiotherapy has been assessed historically, but its use was limited by intestinal toxicity. We recently established the role of Limosilactobacillus reuteri in releasing IL-22 (LR-IL-22) as an effective radiation mitigator, and we have now assessed its effect in an ovarian cancer mouse model. We hypothesized that an LR-IL-22 gavage would enable intestinal radioprotection by modifying the tumor microenvironment and, subsequently, improving overall survival in female C57BL/6MUC-1 mice with widespread abdominal syngeneic 2F8cis ovarian cancer. Herein, we report that the LR-IL-22 gavage not only improved overall survival in mice when combined with a PD-L1 inhibitor by inducing differential gene expression in irradiated stem cells but also induced PD-L1 protein expression in ovarian cancer cells and mobilized CD8+ T cells in whole abdomen irradiated mice. The addition of LR-IL-22 to a combined treatment modality with fractionated whole abdomen radiation (WAI) and systemic chemotherapy and immunotherapy regimens can facilitate a safe and effective protocol to reduce tumor burden, increase survival, and improve the quality of life of a locally advanced ovarian cancer patient.
Keyphrases
- locally advanced
- stem cells
- gene expression
- early stage
- cancer therapy
- mouse model
- squamous cell carcinoma
- randomized controlled trial
- type diabetes
- neoadjuvant chemotherapy
- metabolic syndrome
- drug delivery
- radiation induced
- oxidative stress
- rectal cancer
- lymph node
- adipose tissue
- wild type
- drug induced
- skeletal muscle
- peripheral blood
- diabetic rats
- cell therapy