Related Experiment Video
Updated: Jan 27, 2026

A Novel Feeder-free System for Mass Production of Murine Natural Killer Cells In Vitro
Published on: January 9, 2018
Natural killer cells as a promising therapeutic target for cancer immunotherapy
Nayoung Kim1,2, Hyeon Ho Lee3, Hyo-Jung Lee3,4
1Department of Convergence Medicine, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Abstract:
Natural killer (NK) cells are innate lymphoid cells that provide early protection against cancer development via their selectivity to kill abnormal cells undergoing cellular transformation without the need for prior stimulation. Given the correlation between NK cell dysfunction and cancer prognosis, restoration of endogenous NK cells in the tumor microenvironment or adoptive transfer of NK cells with improved function holds great promise in cancer treatment. Furthermore, MHC-unrestricted tumor lysis by NK cells complements the MHC-restricted killing of tumor cells by cytotoxic T cells, thus positioning NK cells as an alternative or complementary therapeutic target for cancers that are refractory to T cell-based therapy. Although previous therapeutic strategies have focused on the manipulation of NK cell inhibitory receptors, recent advances in our understanding of NK cell activation have provided additional promising strategies to enhance NK cell reactivity against cancer. These approaches include targeting immunosuppressive mechanisms in the tumor microenvironment, such as immune checkpoint receptors, and further enhancing NK cell activation via modulation of intracellular checkpoint molecules or incorporation of tumor-directed chimeric antigen receptors. Thus, an in-depth understanding of NK cell activation will facilitate the optimal design of therapeutic strategies against refractory cancers, possibly in rational and synergistic combination with other therapies.
Insights
Natural killer (NK) cells are crucial for early cancer defense. Enhancing NK cell function offers a promising therapeutic strategy for various cancers, especially those resistant to T cell therapies.
Area of Science:
- Immunology
- Cancer Biology
- Cellular Therapeutics
Background:
- Natural killer (NK) cells are innate lymphoid cells critical for early cancer surveillance.
- NK cell dysfunction is linked to poor cancer prognosis, highlighting their therapeutic potential.
- NK cells offer MHC-unrestricted tumor lysis, complementing T cell-mediated killing and targeting therapy-refractory cancers.
Purpose of the Study:
- To explore novel strategies for enhancing NK cell-based cancer immunotherapy.
- To leverage recent advances in understanding NK cell activation pathways.
- To identify new therapeutic targets for refractory cancers.
Main Methods:
- Reviewing current literature on NK cell biology and cancer immunotherapy.
- Analyzing strategies targeting NK cell inhibitory and activating receptors.
- Investigating methods to overcome tumor microenvironment-induced immunosuppression.
- Exploring the use of chimeric antigen receptors (CARs) for NK cell-directed cancer therapy.
Main Results:
- Recent advances focus on enhancing NK cell reactivity by targeting immunosuppressive tumor microenvironments.
- Modulating intracellular checkpoint molecules and incorporating CARs show promise for boosting NK cell anti-cancer activity.
- Combining NK cell-based therapies with other treatments may yield synergistic effects.
Conclusions:
- Restoring or enhancing NK cell function in the tumor microenvironment is a promising avenue for cancer treatment.
- Targeting NK cell activation pathways, including immune checkpoints and intracellular molecules, offers new therapeutic opportunities.
- A deep understanding of NK cell activation is essential for designing effective combination therapies against refractory cancers.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Tumor Immunotherapy
Nature and Nurture
What is Natural Selection?
Therapeutic Index
Target Cell Response to Hormones
Notably, the cellular response can be regulated by altering the number of receptors expressed in the cell. For example, prolonged exposure to elevated hormone levels results in a gradual decline or down-regulation in the number of receptors for that specific hormone on the cell surface. Conversely, in response to low hormone levels, cells may use up-regulation, producing an...

