Antagonizing the serotonin receptor HTR2B drives antigen-specific cytotoxic T-cell responses and controls colorectal cancer growth.

Neuroimmune communication is known to control various regulatory systems in the body. Serotonin (also known as 5-hydroxytryptamine, HT) is one of the neurotransmitters produced predominantly by enterochromaffin cells in the gut and the neurons of the central nervous system. Immune and cancer cells express several HT receptors (HTRs), and how HTRs modulate various immune pathways and contribute to cancer growth and metastasis is unclear. RNA-seq data analysis shows that human colon adenocarcinoma tissues with high HTR2B expression are associated with poor anti-tumor immune response and poor patient survival. Using an orthotopic mouse model of tumors, we show that HTR2B and other serotonergic molecule expressions are positively associated with colon tumor progression. Antagonizing the HTR2B using specific chemical antagonists significantly suppresses the progression of colon, breast, and melanoma tumors and metastasis in mice by promoting antigen-specific cytotoxic CD8 T cell response and downregulating the PD-L1 expression on tumor cells. Further, treatment with a combination of suboptimal doses of HTR2B antagonists and suboptimal doses of immunotherapy (anti-PD1, anti-PD-L1, or anti-CTLA4 mAb) or chemotherapeutic drugs (5-fluorouracil, oxaliplatin, or irinotecan) showed a robust anti-tumor response and inhibited colon tumor growth. Our finding showed that antagonizing the HTR2B holds a potent therapeutic advantage as a combinatorial regimen of either immunotherapy or chemotherapy to treat colon cancer. One sentence summaryHTR2B expression is associated with colon tumor progression, and antagonizing the HTR2B inhibits tumor growth and metastasis.