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Monitoring the Cancer-Immunity Cycle and Exploring Tumor Microenvironment Dynamics
Published on: June 7, 2024
TIGIT: A Key Inhibitor of the Cancer Immunity Cycle
Nicholas A Manieri1, Eugene Y Chiang1, Jane L Grogan1
1Department of Cancer Immunology, Genentech, South San Francisco, CA, USA.
Abstract:
Immunotherapies that harness the activity of the immune system against tumors are proving to be an effective therapeutic approach in multiple malignancies. Indeed, through accumulation of genetic mutations, many tumors express antigens that can potentially elicit specific tumor immunity. However, tumors can also suppress these responses by activating negative regulatory pathways and checkpoints such as PD-1/PD-L1 and CTLA-4. Blocking these checkpoints on T cells has provided dramatic clinical benefit, but only a subset of patients exhibit clear and durable responses, suggesting that other mechanisms must be limiting the immune response. We discuss here the role of TIGIT, an inhibitory receptor expressed by lymphocytes, in limiting antitumor responses and we review its mechanisms of action during the cancer immunity cycle.
Insights
Cancer immunotherapies show promise, but not all patients respond. This review explores TIGIT, an inhibitory receptor, and its role in limiting anti-tumor immune responses, offering new therapeutic targets.
Area of Science:
- Immunology
- Oncology
- Cancer Research
Background:
- Cancer immunotherapies harness the immune system to fight tumors.
- Immune checkpoints like PD-1/PD-L1 and CTLA-4 are targeted for treatment.
- Durable responses are limited to a subset of patients, indicating other inhibitory mechanisms exist.
Purpose of the Study:
- To discuss the role of the TIGIT inhibitory receptor in limiting anti-tumor immune responses.
- To review TIGIT's mechanisms of action within the cancer immunity cycle.
Main Methods:
- Literature review of TIGIT's function in cancer immunity.
- Analysis of TIGIT's role in immune suppression.
- Exploration of TIGIT's impact on the cancer immunity cycle.
Main Results:
- TIGIT is an inhibitory receptor expressed by lymphocytes.
- TIGIT actively suppresses anti-tumor immune responses.
- Understanding TIGIT mechanisms is crucial for improving immunotherapy efficacy.
Conclusions:
- TIGIT represents a significant barrier to effective anti-tumor immunity.
- Targeting TIGIT may enhance patient responses to cancer immunotherapy.
- Further research into TIGIT pathways is warranted to optimize cancer treatments.
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