Natural Killer (NK) cells are cytotoxic immune cells which play a major role in the immune response against tumors. However, tumor cells can circumvent this immune defense by establishing a microenvironment that prevents the infiltration of NK cells and thus promotes tumor survival and growth.
By studying melanoma, a highly malignant form of skin cancer, Dr Bassam Janji's research team at the Luxembourg Institute of Health (LIH) has revealed a mechanism by which the immunosuppressive environment can be switched to an immunosupportive one. They found that if autophagy - the intracellular recycling process - is blocked in tumor cells, they produce cytokines that attract NK cells. The massive recruitment of NK cells allows killing cancer cells and lets the tumors shrink.
The scientists published their findings in open access in the October issue of the acclaimed scientific journal Proceedings of the National Academy of Sciences of the United States of America (PNAS).
For several years already, it is well known that tumor growth can be reduced by suppressing autophagy in cancer cells. While autophagy blockade is believed to render tumors more sensitive to chemotherapy, its impact on anti-tumor immunity is not well understood. Autophagy can be blocked in tumor cells and mouse models pharmacologically and genetically, the latter by inhibiting the expression of genes involved in the initiation of autophagy, for example BECN1 coding for the protein Beclin-1.
Targeting autophagy impacts on NK cells
The research team of Dr Bassam Janji in the Laboratory of Experimental Cancer Research at LIH's Department of Oncology is specialized in the study of the tumor microenvironment in different types of solid tumors, including skin cancer. In their newly published study, the researchers aimed to investigate the effect of blocking autophagy on the infiltration of NK cells in melanoma.
They found that, when the autophagy process is blocked in tumor cells by inhibiting the expression of BECN1, a large amount of functional NK cells infiltrated into the tumor. This led to a significant reduction in tumor size. The research team revealed that autophagy-defective tumor cells produced an increased amount of CCL5, a small cytokine with chemotactic properties, able to attract NK cells to the tumor bed. When CCL5 is depleted, the infiltration of NK cells and the subsequent regression of tumor volume were no longer observed, thus confirming the crucial role of CCL5 in driving NK cells into autophagy-defective tumors. The researchers further elucidated that the increased production of CCL5 in the absence of autophagy is due to the activation of the kinase JNK and the transcription factor c-Jun.
Using tumor biopsies from melanoma patients, the researchers could show that there is a positive correlation between the production of CCL5 and the infiltration of NK cells. The more CCL5 is produced, the stronger tumors are infiltrated with NK cells. A high level of production of CCL5 was also found to have a positive impact on the survival of melanoma patients.
Directing NK cells to the tumor
This is the first time that a mechanistic link between autophagy and NK cell recruitment could be established. Dr Janji sees a high therapeutic potential in the discovery. "Targeting autophagy in tumor cells is a promising strategy to reinforce the immune system to fight cancer", he claims. "Our study provides a cutting edge advance in the field of cancer immunotherapy and could specifically pave the way for more effective NK cell-based immunotherapies. We now know how we can switch an immunosuppressive tumor environment to an immunosupportive one, enabling the action of NK cells. NK cells have a strong anti-tumor potential, but it can only be exploited if the cells are efficiently directed to the tumor. "
The researchers are now planning to address the impact of targeting autophagy either genetically and pharmacologically on the immune landscape of melanomas by phenotyping other immune cells in the melanoma tumor microenvironment. The ultimate goal of Dr Janji's research team is to provide the proof of concept that targeting autophagy could improve the efficacy of current immunotherapies, notably those based on immune checkpoint blockades.