LEXINGTON, Mass., March 31, 2019 /PRNewswire/ -- Cyteir Therapeutics, a leader in the discovery and development of
Cyteir's platform is based on the groundbreaking discovery of a relationship between activation-induced cytidine deaminase (AID), a DNA-damaging enzyme, and RAD51, a protein that is essential to the repair of DNA breaks. AID overexpression causes elevated DNA damage in high numbers of patients with B-cell malignancies and many patients with solid tumors. Cyteir is developing selective small-molecule compounds that the company believes inhibit RAD51. In preclinical models, reducing the ability of diseased cells to self-repair in this way causes them to become overwhelmed by their own DNA damage and undergo cell death – resulting in the therapeutic effect known as "synthetic lethality." Kevin Mills, Ph.D., Cyteir's co-founder and chief scientific officer, led the research that first identified the synthetic lethality relationship between RAD51 and AID.
"The data being presented at this year's AACR meeting validate the mechanism-of-action underlying our novel synthetic-lethality approach and confirm that we have identified a potent, selective oral inhibitor that has the potential to broadly target multiple cancers with high levels of DNA damage induced by AID," said Markus Renschler, M.D., Cyteir president and CEO. "We are on track to file an IND mid-year and look forward to seeing how this exciting new mechanism performs in clinical trials as we look to improve outcomes for patients with advanced cancers."
Three presentations at AACR 2019 support the potential of CYT-0851 to provide an effective, targeted new treatment option for a variety of hematologic cancers and solid tumors. Data presented by the company today demonstrate in vitro that CYT-0851 is synergistic and may be active as a combination therapy with PARP inhibitors (Poster Section 14, Board 363/24). Researchers tested five PARP inhibitors, each in combination with CYT-0851 in multiple tumor-derived cell lines with varying levels of AID expression and PARP inhibitor sensitivity. Findings suggest that CYT-0851 enhances the synthetic lethal activity of PARP inhibitors and may re-sensitize tumors that are resistant to this class of therapy.
Data scheduled for presentation tomorrow validate – in preclinical models - the mechanism-of-action of CYT-0851 in AID overexpressing cancers, demonstrating that the compound reduces activity of RAD51, reduces levels of DNA repair, and increases levels of DNA damage leading to the death of cancer cells (Poster Section 35, Board 2566/10).
On Wednesday, Cyteir will present data from a preclinical study evaluating the in vivo activity of CYT-0851 in AID-overexpressing B-cell lymphomas and solid tumors, particularly pancreatic cancer (Poster Section 10, Board 4730/20). In this study, oral administration of the compound in three patient-derived pancreatic cancer xenograft models led to significant anti-tumor activity.
About Cyteir Therapeutics
Cyteir Therapeutics is a leader in the discovery and development of novel therapeutics based on the biology of DNA repair. It is the first company to date that is pursuing a "gain-of-function" approach to synthetic lethality for the treatment of cancer and autoimmune diseases, such as type 1 diabetes, systemic lupus erythematosus and multiple sclerosis. In contrast to other approved synthetic lethality therapies (including PARP inhibitors), which are used to treat cancers with DNA mutations that cause loss-of-function in specific genes such as BRCA, Cyteir is targeting diseases with a gain-of-function in AID. Abnormal gain of AID function occurs in a wide range of cancers and autoimmune diseases but not in healthy tissues. Cyteir's lead molecules were initially discovered using the company's drug discovery platform, which enables identification of primary cells with tunable genetic constraints. Cyteir is backed by leading healthcare investors, including Venrock, Lightstone Ventures, Osage University Partners, DROIA Oncology Ventures as well as Celgene. For more information, visit www.cyteir.com.
MEDIA CONTACT:Michele ParisiFor Cyteir Therapeutics925firstname.lastname@example.org
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SOURCE Cyteir Therapeutics
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