Hollings researchers uncover new targets for breast cancers resistant to standard therapies

Researchers at MUSC Hollings Cancer Center believe that some drugs already approved by the U.S. Food and Drug Administration or currently in clinical trials could be repurposed for certain breast cancer patients whose cancer has become resistant to standard therapies.

Ozgur Sahin, Ph.D., a professor and SmartState Endowed Chair in the Department of Biochemistry and Molecular Biology, led the research, which was published Nov. 2 in Nature Communications.

The research, funded by an American Cancer Society Research Scholar Grant, started as an investigation into cancer resistance to the drug tamoxifen but expanded as the research questions led down new avenues, encompassing other hormone therapies and CDK4/6 inhibitors. CDK4/6 inhibitors are targeted therapies that stop cancer cells from multiplying.

The result is a new explanation of why certain widely used therapies work – and by better understanding how these common therapies are actually functioning, researchers can formulate new therapies to respond when they stop working.

Christina Annunziata, M.D., Ph.D., senior vice president for extramural discovery science at the American Cancer Society, praised the work.

“The American Cancer Society is proud to support Dr. Sahin’s research into overcoming resistance to therapy in ER-positive breast cancer. This study underscores his novel approach to understanding molecular mechanisms of resistance underlying metastatic recurrence; as such, his research helps advance our mission to ensure that everyone has an opportunity to prevent, detect, treat and survive cancer,” she said.

“The most important thing here is that there are inhibitors for all those three which are either FDA-approved for different cancers, or they are in clinical trials for other non-cancer diseases."

Ozgur Sahin, Ph.D.

Sahin focused on estrogen receptor positive, or ER-positive, breast cancer. ER-positive breast cancer, which accounts for about 75% of all breast cancer cases, uses estrogen to grow. Women with ER-positive breast cancer may use hormone therapy after surgery to prevent the cancer from returning or, if the cancer has already spread, they may use it to slow or stop its spread. CDK4/6 inhibitors may be used at the same time as or after hormone therapy, depending on the specific diagnosis.

However, some patients may find that their cancer develops resistance to hormone therapy and CDK4/6 inhibitors.

“What we wanted to do in this study was to identify the initial question of how these therapies work and why they don't work when patients develop resistance. And the third thing is – how we can make them work again?” Sahin said.

Cancer drugs are broadly divided into two categories based on how they act. Cytotoxic drugs kill cancer cells and cytostatic drugs slow or prevent cancer growth.

Hormone therapy has been categorized as cytostatic because it blocks estrogen receptors, but Sahin said his team found a new mechanism by which hormone therapy, also called endocrine therapy, is acting.

“What we show here is they are actually inducing DNA damage like chemotherapy agents,” he said. “This is so surprising and intriguing because we've found that these endocrine therapies and CDK4/6 inhibitors induce DNA damage with inhibition of homologous recombination, leading to toxic PARP trapping and cell death.” Recombination is a process by which pieces of DNA are broken and recombined to produce new combinations. PARP is a key protein involved in DNA repair.

“And since PARP is trapped on the chromatin, the transcription [the process of copying a gene’s instructions onto messenger RNA in order to build proteins] cannot happen. This is beyond the known blockage of estrogen receptor-dependent transcription by endocrine therapies,” he explained.

 

“We show that this is happening because when we give the standard-of-care therapies, they induce cyclic AMP,” added Ozge Saatci, a senior graduate student in the Sahin Lab and the first author of the paper. “These are second messengers in the cells. They are small molecules, and they have a lot of functions, but since these standards-of-care therapies lead to accumulation of cyclic AMP, so they generate reactive oxygen species, which leads to DNA damage.”

Sahin added that when cancer cells become resistant to hormone therapy, what is actually happening is that the cancer is becoming less dependent on estrogen to grow. Instead, it turns to other molecules like epidermal growth factor, or EGF.

Sahin’s team showed that targeting epidermal growth factor receptors (EGFR) or phosphodiesterase or using PARP inhibitors would overcome the cancer’s resistance to standard therapies.

“The most important thing here is that there are inhibitors for all those three which are either FDA-approved for different cancers, or they are in clinical trials for other non-cancer diseases,” Sahin said.

For example, a phosphodiesterase 4D inhibitor is in clinical trials for Fragile X Syndrome, a genetic disorder that causes developmental delays and intellectual disabilities, particularly in boys. Another clinical trial is testing PARP inhibitors in combination with endocrine and CDK 4/6 inhibitors. However, Sahin noted that the trial targets patients with BRCA mutations, and his team’s research indicates that the PARP inhibitors could also work for patients without BRCA mutations.

This work was supported by research funding from American Cancer Society Research Scholar Grant RSG-19-194-01-CSM (O.S.), and in part, from the National Institutes of Health (NIH; R01CA267101 and R01CA251374 to O.S.), SmartState Endowment in Lipidomics and Drug Discovery (O.S.) and Susan G. Komen Interdisciplinary Graduate Training to Eliminate Cancer Disparities (IGniTE-CD) GTDR17500160 (Ozge.S). The core facilities utilized are supported by NIH (C06 RR015455), Hollings Cancer Center Support Grant (P30 CA138313), or Center of Biomedical Research Excellence (Cobre) in Lipidomics and Pathobiology (P30 GM103339). The Zeiss 880 microscope was funded by a Shared Instrumentation Grant (S10 OD018113). 

The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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