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Biology behind new drug used to treat triple-negative breast cancer uncovered

07.14.23 | Georgetown University Medical Center

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WASHINGTON – How TTP488 (azeliragon), an experimental drug, impairs aggressive, triple-negative breast cancer from metastasizing has been uncovered at the cellular level, according to researchers at Georgetown University’s Lombardi Comprehensive Cancer Center who worked in collaboration with scientists at the University of Miami, Florida.

The finding appeared July 13, 2023, in Nature Breast Cancer.

Triple-negative breast cancers (TNBCs) account for about 10-15% of all diagnosed breast cancers and are comprised of cancer cells that don’t have estrogen or progesterone receptors, nor do they produce a protein called HER2 in significant quantities. TNBC’s are more common in women younger than age 40 or those who are Black; for those cancers that metastasize, the five-year survival rate is only 12%.

TNBCs have eluded effective treatment for decades. This discovery pinpoints some of the signaling pathways and cellular mechanisms through which a receptor that sits on the surface of TNBC cells, called the Receptor for Advanced Glycation End-products (RAGE), regulates its deadly metastatic spread. Armed with this knowledge, the researchers were able to test the effectiveness of TTP488 in both the lab and in mice to show that the drug could be helpful in people.

“A clinical trial that is now underway at Lombardi and other cancer centers is a direct result of this pre-clinical research on RAGE inhibitors that started at the University of Miami and has continued with my move to Lombardi,” says Barry Hudson, PhD, associate professor of oncology at Georgetown Lombardi and corresponding author for this article. “Our study is the first to show that TTP488 impairs breast cancer metastasis in cells and rodents. It is the only RAGE inhibitor that is approved for use in humans, so the implications for clinical trials are manyfold and we hope that progress against triple-negative breast cancers will be rapid.”

RAGE was discovered in 1992 as a possible factor involved in vascular complications of diabetes. It has subsequently been shown to be involved in a broad range of diseases due to its nefarious ability to bind many different molecules and induce inflammation. Based on this knowledge, TTP488 was developed in the 2000s for Alzheimer disease, but trial results of the drug were equivocal. However, armed with more recent knowledge about its biology and effects, including its broad availability across many biological systems and its encouraging safety profile, it now appears to be a very promising candidate for clinical trials.

The investigators started their study by looking at two RAGE inhibitors: TTP488 and FPS-ZM1, both of which impaired spontaneous and experimental metastasis of TNBC in mice. But after extensive study in the lab and in mice, TTP488 was clearly the more effective drug and the one they pursued extensively enough to see if it qualified for use in people in a clinical trial. TTP488 still needs to be tested in larger, more advanced clinical trials to prove its true effectiveness so it is not yet available to women outside of those enrolled in clinical trials.

The investigators also identified three important pathways that could drive RAGE inhibition: Pyk2, STAT3, and Akt. This finding will help researchers better understand the mechanisms by which RAGE drives metastasis, potentially enabling combination therapeutic approaches targeting RAGE and these pathways.

“We are currently testing different combinations of TTP488 with other anti-cancer therapies to determine if RAGE inhibitors can synergize with those therapies,” says Hudson. “I think the outlook for effectively treating triple-negative breast cancers has become much brighter of late.”

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In addition to Hudson, other authors at Georgetown University include Melinda Magna, Alec McIntosh, Katherine Drews-Elger, Masaru Takabatake, Adam Ikeda, Philip Miller and Marc E. Lippman. Gyong Ha Hwang, Barbara J. Mera and Taekyoung Kwakare are at the University of Miami, Florida.

This research was supported by the Florida Department of Health and by the METAvivor Foundation.

The authors declare that Hudson and Lippman have a patent publication (WO 2019/094613) on the use of RAGE inhibitors to treat breast cancer (patent application has not been pursued). The authors declare no competing non-financial interests.

About Georgetown University’s Lombardi Comprehensive Cancer Center
Georgetown’s Lombardi Comprehensive Cancer Center is designated by the National Cancer Institute (NCI) as a comprehensive cancer center. A part of Georgetown University Medical Center, Georgetown Lombardi is the only comprehensive cancer center in the Washington D.C. area. It serves as the research engine for MedStar Health, Georgetown University’s clinical partner. Georgetown Lombardi is also an NCI recognized consortium with John Theurer Cancer Center/Hackensack Meridian Health in Bergen County, New Jersey. The consortium reflects an integrated cancer research enterprise with scientists and physician-researchers from both locations. Georgetown Lombardi seeks to improve the diagnosis, treatment, and prevention of cancer through innovative basic, translational and clinical research, patient care, community education and outreach to service communities throughout the Washington region, while its consortium member John Theurer Cancer Center/Hackensack Meridian Health serves communities in northern New Jersey. Georgetown Lombardi is a member of the NCI Community Oncology Research Program (UG1CA239758). Georgetown Lombardi is supported in part by a National Cancer Institute Cancer Center Support Grant (P30CA051008). Connect with Georgetown Lombardi on Facebook (Facebook.com/GeorgetownLombardi) and Twitter (@LombardiCancer).

About Georgetown University Medical Center
Georgetown University Medical Center (GUMC) is an internationally recognized academic health and science center with a four-part mission of research, teaching, service and patient care (through MedStar Health). GUMC’s mission is carried out with a strong emphasis on public service and a dedication to the Catholic, Jesuit principle of cura personalis -- or “care of the whole person.” The Medical Center includes the School of Medicine and the School of Nursing & Health Studies, both nationally ranked; Georgetown Lombardi Comprehensive Cancer Center, designated as a comprehensive cancer center by the National Cancer Institute; and the Biomedical Graduate Research Organization, which accounts for the majority of externally funded research at GUMC including a Clinical and Translational Science Award from the National Institutes of Health. Connect with GUMC on Facebook (Facebook.com/GUMCUpdate) and Twitter (@gumedcenter).

Breast Cancer

10.1038/s41523-023-00564-9

Experimental study

Animals

RAGE Inhibitor TTP488 (Azeliragon) Suppresses Metastasis in Triple- 2 Negative Breast Cancer

13-Jul-2023

Keywords

Article Information

Contact Information

Karen Teber
Georgetown University Medical Center
km463@georgetown.edu

How to Cite This Article

APA:
Georgetown University Medical Center. (2023, July 14). Biology behind new drug used to treat triple-negative breast cancer uncovered. Brightsurf News. https://www.brightsurf.com/news/80E4PMQ8/biology-behind-new-drug-used-to-treat-triple-negative-breast-cancer-uncovered.html
MLA:
"Biology behind new drug used to treat triple-negative breast cancer uncovered." Brightsurf News, Jul. 14 2023, https://www.brightsurf.com/news/80E4PMQ8/biology-behind-new-drug-used-to-treat-triple-negative-breast-cancer-uncovered.html.