From left to right, Clara Gómez-Aleza, Guillermo Yoldi and Eva González-Suárez. /Idibell
The team of Eva González-Suarez, from the CNIO and IDIBELL, and the team of Christos Sotiriou, from the Jules Bordet Institute, demonstrate that a drug already used to treat osteoporosis promotes the infiltration of immune cells in breast tumours
These findings propose a new target to increase the antitumor immune response and make breast cancer more sensitive to immunotherapy
Despite the success of immunotherapy in the treatment of cancers such as lung or melanoma, it is still not effective in breast cancers for being ‘cold’, with low infiltration of immune cells. Tumours use strategies to evade immune surveillance by reducing the infiltration of cells that could attack them or by attracting immunosuppressive cells. These strategies can contribute to the poor prognosis observed in breast cancer of young women and make them unresponsive to immunotherapy. For this reason, the identification of a therapy that could convert immunologically ‘cold’ tumours -in which immunotherapy is not effective- into ‘warm’ tumours would represent an important step to increase the efficiency of immunological therapies for breast cancer, since these are based on the reactivation of immune cells to attack tumour cells.
In an article published today in the journal Nature Communications, the Transformation and Metastasis Group led by Eva Gonzalez-Suarez, first from the Bellvitge Institute for Biomedical Research (IDIBELL) and currently at the Spanish National Cancer Research Center (CNIO), proposes RANK signalling pathway as a key candidate to modulate the immune response in breast tumours. Furthermore, in collaboration with Christos Sotiriou, from the Jules Bordet Institute in Belgium, RANK pathway’s immunomodulatory activity has been confirmed in a clinical trial with premenopausal patients with luminal breast cancer, one of the most resistant types to immunotherapy.
The study reports that the inhibition of RANK protein promotes the recruitment of immune cells within the tumor in mouse models and in patients with breast cancer. In addition, tumors appear to be more sensitive to immunotherapy after inhibiting RANK pathway in tumor cells. These results suggest that this protein is playing an essential role in the communication between tumor and immune cells. Furthermore, they point to RANK pathway as a possible escape route of cancer cells against immunotherapy.
The clinical trial led by Christos Sotiriou with cancer patients with premenopausal breast early stage showed that patients tolerate the administration of a monoclonal antibody that inhibits RANK, achieved good results enhancing infiltration of immune cells in tumours and identified biomarkers that could help select patients who would benefit from therapy.
The strength of this work lies in the fact that two independent studies, a clinical trial and preclinical research, conclude that inhibition of RANK signalling enhances antitumor immune response.
González-Suárez indicates that “the monoclonal antibody being tested in this study is used routinely for the treatment of bone diseases such as osteoporosis and bone metastases, but not for cancer treatment. Our results support the use of this antibody in combination with immunotherapy against breast cancer,” and adds: “This strategy could turn immunologically cold breast cancers into tumours sensitive to the immune system activity.”
Tumour immune surveillance
The immune system, which recognizes foreign microorganisms, viruses and bacteria, and provides a response to destroy these disease-causing agents, plays a similar role in protecting the body against malignancies. Cancer cells express abnormal proteins that can be recognized by immune cells because they act as tags that allow the immune system to find and destroy those cells.
The presence of immune cells within the tumour, the so-called immune infiltration, is associated with a good prognosis. However, tumours have mechanisms that allow them to escape the immune responses that often prevent the development of malignant tumours, which means that immunotherapy is not yet fully effective in the treatment of various types of cancer. Studies like the one now published by IDIBELL and CNIO contribute to improving this promising strategy for cancer treatments.
The study has been funded by the Ministry of Science and Innovation, the National Institute of Health Carlos III, the European Research Agency, the European Regional Development Fund, the La Marató de TV3 Foundation, the National Fund for Scientific Research of Belgium, Televie, the US National Institutes of Health, and Amgen.
Inhibition of RANK signaling in breast cancer induces an anti-tumor immune response orchestrated by CD8+ T cells. Clara Gómez-Aleza et al (Nature Communications, 2020). DOI: 10.1038/s41467-020-20138-8