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Profiling Sensitivity to Targeted Therapies in EGFR-Mutant NSCLC Patient-Derived Organoids
Published on: November 22, 2021
Immune regulation of therapy-resistant niches: emerging targets for improving anticancer drug responses
1Research Center for Infection-associated Cancer, Institute for Genetic Medicine, Hokkaido University, Kita 15, Nishi 7, Kita-ku, Sapporo, Hokkaido, 060-0815, Japan, jinushi@igm.hokudai.ac.jp.
Abstract:
Emerging evidence has unveiled a critical role for immunological parameters in predicting tumor prognosis and clinical responses to anticancer therapeutics. On the other hand, responsiveness to anticancer drugs greatly modifies the repertoires, phenotypes, and immunogenicity of tumor-infiltrating immune cells, serving as a critical factor to regulate tumorigenic activities and the emergence of therapy-resistant phenotypes. Tumor-associated immune functions are influenced by distinct or overlapping sets of therapeutic modalities, such as cytotoxic chemotherapy, radiotherapy, or molecular-targeted therapy, and various anticancer modalities have unique properties to influence the mode of cross-talk between tumor cells and immune cells in tumor microenvironments. Thus, it is critical to understand precise molecular machineries whereby each anticancer strategy has a distinct or overlapping role in regulating the dynamism of reciprocal communication between tumor and immune cells in tumor microenvironments. Such an understanding will open new therapeutic opportunities by harnessing the immune system to overcome resistance to conventional anticancer drugs.
Insights
Immunological factors predict cancer prognosis and treatment response. Understanding how therapies affect immune cell interactions is key to overcoming drug resistance and improving cancer treatment.
Area of Science:
- Immunology
- Oncology
- Cancer Therapeutics
Background:
- Immunological parameters are crucial for predicting tumor prognosis and response to anticancer therapies.
- Anticancer drug responsiveness alters tumor-infiltrating immune cells, impacting tumor growth and therapy resistance.
- Different anticancer modalities uniquely influence immune cell interactions within the tumor microenvironment.
Purpose of the Study:
- To elucidate the molecular mechanisms by which distinct anticancer strategies modulate the communication between tumor and immune cells.
- To understand the overlapping and unique roles of various therapeutic modalities in regulating immune cell dynamics within the tumor microenvironment.
Main Methods:
- Review and analysis of emerging evidence on the interplay between cancer therapies and the tumor immune microenvironment.
- Examination of molecular machineries governing immune cell regulation by cytotoxic chemotherapy, radiotherapy, and molecular-targeted therapy.
Main Results:
- Anticancer treatments significantly modify immune cell repertoires, phenotypes, and immunogenicity.
- Therapeutic modalities exert distinct or overlapping influences on tumor-associated immune functions and tumor-immune cell cross-talk.
- Understanding these interactions is essential for predicting treatment outcomes and resistance.
Conclusions:
- Precise understanding of how anticancer strategies regulate tumor-immune cell communication is critical.
- Harnessing the immune system based on this understanding may offer new avenues to overcome resistance to conventional anticancer drugs.
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