A study led by researchers at the Hospital del Mar Research Institute advances one of the most significant milestones in breast cancer treatment, making immunotherapy effective against the most common tumour type, oestrogen receptor-positive or luminal breast cancer.

This subtype accounts for 70% of breast cancer cases, and despite effective treatments, it causes the highest mortality in total cases.

Additionally, immunotherapy is not effective or approved because it shows no immune system response in these tumours, except in a minority subgroup that, precisely, has low oestrogen receptor levels.

The work is published by The Journal of Clinical Investigation and led by Dr. Toni Celià-Terrassa’s team from the Cancer Stem Cells and Metastasis Dynamics Laboratory at the Hospital del Mar Research Institute.

The study is supported by Ausonia through the Spanish Association Against Cancer.

The study highlights the importance of the oestrogen receptor in the tumour’s strategy to evade immune system action.

By analysing public data from various clinical trials, the researchers found that this factor limits immune system infiltration and prevents immunotherapy from being effective.

In contrast, inhibiting the oestrogen receptor allows the activation of LCOR and interferon signals, both factors related to antigen presentation mechanisms on the cell surface, making the tumour cell visible to the immune system.

The next step was to generate a preclinical model in animal models, which confirmed this tumour protection mechanism.

They also found that the LCOR molecule, which in other preclinical studies in triple-negative breast cancer increased the effectiveness of immunotherapy, was ‘sequestered’ by the oestrogen receptor and could not perform this function.

"The oestrogen receptor sequesters LCOR and prevents it from activating the antigen-presenting machinery, conditioning its function and not allowing the tumour to become 'visible'," explains Dr. Toni Celià-Terrassa, coordinator of the Cancer Stem Cells and Metastasis Dynamics Laboratory at the Hospital del Mar Research Institute.

To address this effect, the research team used two strategies in the preclinical setting.

First, they combined LCOR and immunotherapy with hormonal inhibitors, or endocrine therapy, already used to treat this type of cancer.

Second, they created a modified version of LCOR (LSKAA) that prevents sequestration by the oestrogen receptor.

“Under normal conditions, oestrogen signalling is prevalent in this type of tumour and prevents LCOR from acting. If we manage to break this signalling with antiestrogen therapy, LCOR activates antigen presentation and opens the path for immunotherapy,” adds José Ángel Palomeque, researcher at the Hospital del Mar Research Institute.

This modified LCOR escapes the oestrogen receptor’s action and enhances antigen presentation, necessary for immune attack.

In this regard, the RNA therapy generation laboratory at the Hospital del Mar Research Institute uses this technology to create modified LCOR therapies that do not interact with the oestrogen receptor in combination with immunotherapy.

Additionally, the recently established spin-off VIOLET Pharmaceuticals focuses on these types of therapies.

Dr. Joan Albanell, head of the Medical Oncology Service at the Hospital del Mar and director of the Cancer Research Programme at the Hospital del Mar Research Institute, states that "this study opens the door to a new strategy to sensitise this subtype of breast cancer to immunotherapy." The goal is to work towards "turning this modified LCOR into a therapy that can be investigated in upcoming clinical trials, especially for patients with tumours that present oestrogen receptors, which currently limit the effectiveness of immunotherapy," he explains.

Source: IMIM (Hospital del Mar Medical Research Institute)