Interferon-γ increases sensitivity to chemotherapy and provides immunotherapy targets in models of metastatic castration-resistant prostate cancer

Interferon-gamma (IFN gamma) is a cytokine with limited evidence of benefit in cancer clinical trials to date. However, it could potentially play a role in potentiating anti-tumor immunity in the immunologically cold metastatic castration-resistant prostate cancer (mCRPC) by inducing antigen presentation pathways and concurrently providing targets for immune checkpoint blockade therapy. Moreover, it could additionally increase sensitivity to chemotherapy based on its pleiotropic effects on cell phenotype. Here, we show that IFN gamma treatment induced expression of major histocompatibility class-I (MHC-I) genes and PD-L1 in prostate cancer cells in vitro. Furthermore, IFN gamma treatment led to a decrease in E-cadherin expression with a consequent increase in sensitivity to chemotherapy in vitro. In an in vivo murine tumor model of spontaneous metastatic prostate cancer, IFN gamma systemic pretreatment upregulated the expression of HLA-A and decreased E-cadherin expression in the primary tumor, and more importantly in the metastatic site led to increased apoptosis and limited micrometastases in combination with paclitaxel treatment compared to diffuse metastatic disease in control and monotherapy treatment groups. These findings suggest that IFN gamma may be useful in combinatorial regimens to induce sensitivity to immunotherapy and chemotherapy in hepatic metastases of mCRPC.

Automated summary

Interferon-gamma (IFN gamma) has the potential to enhance anti-tumor immunity in immunologically cold metastatic castration-resistant prostate cancer (mCRPC) by inducing antigen presentation pathways and increasing sensitivity to chemotherapy. Experimental results showed that IFN gamma treatment in prostate cancer cells induced the expression of specific genes in vitro and led to increased sensitivity to chemotherapy; in a mouse model of metastatic prostate cancer, IFN gamma pretreatment upregulated gene expression and increased apoptosis in the metastatic site.