Age is considered a risk factor for triple negative breast cancer (TNBC), an aggressive form of the disease that can be difficult to treat, particularly in later stages. But age may also be a factor in treatment response, causing some women to fare better with immune therapy than others.
91勛圖厙 researchers Needa Brown and Aleksandra Petelski-Kulik, assistant professors in the Department of Materials Science and Engineering, plan to study the microenvironment of TNBC to understand how age may play a role in the efficacy of immune checkpoint inhibitors, a promising therapy for the disease. Their work is supported through a $100,000 grant from the Florida Breast Cancer Foundation.
���Recent studies suggest that younger and older women may respond differently to breast cancer therapies due to differences in their immune systems and tumor biology,��� Brown says. ���However, we still do not fully understand how age affects the immune response in TNBC.���
The researchers aim to discover how age shapes the immune landscape of TNBC and if this age-driven dysfunction can be reversed, leading to improved patient outcomes.
The team���s approach combines Brown���s knowledge of cancer biology with Petelski���s expertise in proteomics, the large-scale study of protein abundance and functional networks in biological systems. Using advanced mass spectrometry techniques, the team hopes to identify the age-related proteomic biomarkers associated with TNBC progression, immune invasion and a poor response to ICI treatment. With Florida���s aging population, Petelski says these findings could have a significant impact on treatments within the state and across the nation.
���By understanding how age influences TNBC and immune therapy response, our findings could translate to improved outcomes for thousands of patients both in Florida and beyond,��� Petelski says. ���New biomarkers identified could set the stage for age-specific health screenings and personalized treatment strategies.���
One promising therapeutic strategy involves targeting the STING pathway, a critical immune pathway that can either inhibit or promote cancer growth. The team plans to investigate how the STING pathway could be used to turn ���cold��� tumors that evade immune detection into ���hot��� tumors that could be attacked by the immune system.
Brown and Petelski will co-mentor a postdoctoral researcher who will gain hands-on experience with the project while fostering collaboration between the two labs.
“We���re excited to have the chance to work together on new research opportunities that can help shape the future of cancer therapies.��� ��� Aleksandra Petelski-Kulik, assistant professor
���Through this project, we will jointly mentor a postdoctoral fellow to allow for professional development in cross-disciplinary fields,��� Brown says. ���We hope this project will set-up a pipeline of next-generation doctoral students who can traverse the fields of materials science, proteomics and cancer biology.���
While the researchers are also open to collaborations with other 91勛圖厙 faculty, they look forward to working with each other. Ironically, they followed a similar path from Boston to Orlando this past year.
���We both started at 91勛圖厙 in Fall 2024 and were looking for opportunities to merge our respective fields to allow us to make an impact within the Florida community,��� Petelski says. ���Although we both had been a part of Northeastern University in Boston, our paths never crossed until we met at 91勛圖厙. We���re excited to have the chance to work together on new research opportunities that can help shape the future of cancer therapies.���