Our Research Focus
We investigate how diverse cancers survive by evading immune attack, dissecting the cellular, genetic, and microenvironmental mechanisms—such as altered antigen presentation, suppressive myeloid and regulatory lymphoid populations, and mutation-driven neoantigen loss—that permit immune escape. Our ultimate goal is to translate those insights into novel therapeutic strategies that reprogram the tumor microenvironment, restore effective antitumor immunity, and overcome resistance to existing treatments through targeted combination therapies, biomarker-guided patient selection, and engineered immune effectors to ultimately convert immunologically “cold” tumors into “hot” tumors responsive to durable immune control.
Latest Publications
Targeting DHX9 Triggers Tumor-Intrinsic Interferon Response and Replication Stress in Small Cell Lung Cancer Cancer Discov. (2024) Murayama T, Nakayama J, Jiang X, Miyata K, Morris AD, Cai KQ, Prasad RM, Ma X, Efimov A, Belani N, Gerstein ER, Tan Y, Zhou Y, Kim W, Maruyama R, Campbell KS, Chen L, Yang Y, Balachandran S, Cañadas I.
Our recent study found that DHX9 suppresses tumor-intrinsic innate immune responses and increases replication stress, making it a promising therapeutic target for small cell lung cancer (SCLC).
Ongoing Projects