New treatment for aggressive breast cancer
Researchers have uncovered a way to treat aggressive tumours through manipulation of the connective tissue cells of the tumour.
Approximately 10-15% of breast cancer cases do not respond to treatment with hormone therapy, which means that they are more aggressive and often recur.
The international research team, led by researchers at Lund University in Sweden, are now developing a new drug that transforms aggressive breast cancer so that it becomes responsive to standard hormone therapy.
Cancer occurs as a result of mutations and other genetic changes that disable the growth control system normally present in our cells. However, new studies emphasise the importance of the communication of cancer cells with other cell types in the surrounding tissue, such as connective tissue, blood vessels and immune system cells, that enable the tumours to form, spread and resist treatment.
Breast cancer is one of the tumour types that is richest in connective tissue, providing a rationale for a major role of connective tissue cells in tumour growth.
There are a number of different types of breast cancer, each with different prognoses and treatment options. Patients with breast cancers that are hormone-sensitive (around 70% of all patients) have the best prognosis, whereas approximately 10-15% of patients have cancers that are insensitive to hormones and more aggressive (basal breast cancer). Basal breast cancers typically require more intensive treatment with chemotherapy, which may be associated with severe side effects.
“Our studies of the communication between breast cancer cells and their surrounding tissue have revealed a growth factor – PDGF-CC – which transmits information between the tumour cells and the connective tissue cells, mainly in basal breast cancers. Detailed analyses of around 1,400 breast cancers showed that high levels of PDGF-CC in the tumour cells were associated with a poor prognosis,” explains cancer researcher Kristian Pietras, Professor at Lund University.
Professor Pietras led a multidisciplinary and international research team based at the Lund University Cancer Centre at Medicon Village, in collaboration with researchers from Karolinska Institutet, the Olivia Newton-John Cancer Research Institute in Melbourne Australia, and University Hospital Bonn, in this ground-breaking research.
“Previously, it was believed that the various subgroups of breast cancer originated from different cell types in the mammary gland. Our research has shown that connective tissue cells can also modify tumour cells directly with regard to their sensitivity to hormones, which has significant implications in the development of more effective treatments,” states Professor Ulf Eriksson at Karolinska Institutet, a co-investigator of the study.
In experimental models, the researchers tested a new biological drug they have developed which blocked the PDGF-CC-mediated communication between the tumour cells and the connective tissue cells. Remarkably, this resulted in the transformation of the basal breast cancers into hormone-sensitive luminal breast cancers. As a consequence of this transformation, the tumours then became highly responsive to conventional hormone therapy.
“We have thus developed a new treatment strategy for aggressive and difficult-to-treat breast cancers that restores sensitivity to hormone therapy. These findings have major implications in the development of more effective treatments for patients with aggressive breast cancer,” concludes Kristian Pietras.
About the study
Six different research teams at the Lund University Cancer Centre at Medicon Village contributed to the study with valuable expertise in oncology, pathology, genomics, bioinformatics, animal models, experimental treatment studies and cell and molecular biology. The study was initiated by Professor Kristian Pietras together with Professor Ulf Eriksson at Karolinska Institutet in Stockholm. The research team also includes several international collaboration partners, whose expertise, not least within the development of biological drugs (Professor Andrew Scott, Olivia Newton-John Cancer Research Institute, and La Trobe University, Melbourne) and pathology (Professor Glen Kristiansen, University Hospital, Bonn) was essential to the success of the project.
The study was funded to a large extent by a donation from Göran and Birgitta Grosskopf, as well as research funding from the European Research Council (TUMORGAN project), the Swedish Cancer Society, the Swedish Research Council, and the National Health and Medical Research Council Australia.