Epigenetic Key Unlocks Treatment Path for Endocrine-Resistant Breast Cancer

Endocrine resistance – a major cause of breast cancer deaths – can be underpinned by an epigenetic change called DNA methylation, researchers at the Garvan Institute of Medical Research have discovered. The team successfully reversed this methylation to reduce cancer growth in patient-derived animal models.

Using a low dose of the epigenetic therapy drug decitabine, which is currently used to treat some blood cancers, the researchers significantly suppressed the growth of endocrine-resistant breast tumours in mice and increased survival time by 90%. The finding, which will be tested in a future Phase I clinical trial, is a potential gamechanger for the more than 4,000 people who are diagnosed with endocrine-resistant breast cancer each year in Australia alone.

"This research has uncovered a completely new approach to treating endocrine-resistant breast cancer. In our study, we have not only pinpointed a new molecular mechanism that explains how endocrine resistance might develop – we have identified a treatment currently used in the clinic that can target this mechanism precisely," says Professor Susan Clark, Head of the Cancer Epigenetics Laboratory at Garvan and senior author of the paper published in Nature Structural & Molecular Biology.

Epigenetic Change Drives Breast Cancer Treatment Resistance

An estimated 70% of all diagnosed breast cancers are oestrogen receptor positive (ER+), which means their growth is activated by oestrogen – a hormone that plays a key role in sexual and reproductive health in women. While endocrine therapy that suppresses oestrogen in the body can slow or stop the growth of these tumours, more than 30% of patients develop resistance, with their tumours no longer requiring oestrogen to grow.

In a 2020 study, the Garvan team investigated the endocrine-resistant cancer's epigenome, the layer of instructions that organises and regulates DNA's activity, and revealed that endocrine resistance is linked to methyl groups attaching to regulatory regions of DNA and changing the 3D structure of DNA inside cancer cells.

New Approach to Breast Cancer Therapy

In this current study, we set out to reverse the abnormal methylation patterns and restore the 3D DNA structure in the endocrine-resistant ER+ breast cancers using epigenetic therapy. We found that decitabine removed methyl groups at specific DNA regulatory regions, rewiring the 3D structure of DNA to not only reactivate the production of oestrogen receptors, but also activate tumour suppressor genes that can reduce cancer growth."

Dr Joanna Achinger-Kawecka, First Author, Head of the 3D Epigenome in Cancer Group at Garvan

"After treating patient-derived endocrine resistant breast cancer tumours with decitabine alone, we were surprised to see cancer growth significantly reduced in mice," says co-first author Associate Professor Clare Stirzaker, Head of the Epigenetic Biomarker Group. "This highlights the importance of studying fundamental molecular mechanisms to best guide targeted treatments."

Decitabine is an FDA- and TGA-approved epigenetic therapy currently used to successfully treat certain blood cell cancers, including myelodysplastic syndromes, but there are limited studies in other cancers. While the current study focused on ER+ breast cancer, the researchers say the drug may also have potential for other endocrine-resistant cancers driven by epigenetic changes.

"The next stage of our research will be to test decitabine together with endocrine therapy, which could be even more effectively target this difficult-to-treat cancer," says Professor Clark. "We hope that such a combination approach is a turning point that enables significantly better clinical outcomes."

Journal reference:

Achinger-Kawecka, J., et al. (2024). The potential of epigenetic therapy to target the 3D epigenome in endocrine-resistant breast cancer. Nature Structural & Molecular Biology. doi.org/10.1038/s41594-023-01181-7.


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of AZoLifeSciences.
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