Combination breast cancer therapy targets tumor cells and the blood vessels that feed them

breast cancer
Three-dimensional culture of human breast cancer cells, with DNA stained blue and a protein in the cell surface membrane stained green. Image created in 2014 by Tom Misteli, Ph.D., and Karen Meaburn, Ph.D. at the NIH IRP.

Each day, normal human cell tissues express a protein known as p53 that wages war against potential malignancies. However, between 30 and 40 percent of human breast cancers express a defective (mutant) form of p53 that helps cancer cells proliferate and grow. Now, researchers at the University of Missouri have found that combining a cancer therapy, which activates mutant p53 and is currently under a clinical trial, with a second drug therapy that helps suppress tumor blood vessels found in cancer cells, can help significantly reduce the spread of breast cancer tumors while also causing cancer cell death.

In a majority of cases, a mutated p53 protein exists. Mutated p53 plays a key role in promoting tumor and helps in the development of that supply oxygen and other nutrients the tumor needs to grow. However, a specific molecule known as APR-246, which is the drug currently under a human clinical trial, has the ability to restore p53 function giving the body the tools it needs to fight cancer.

"In order to effectively treat tumors, therapeutics are being developed that target mutant proteins that help grow ; APR-246 is one of those drugs," said Salman Hyder, the Zalk Endowed Professor in Tumor Angiogenesis and professor of biomedical sciences in the College of Veterinary Medicine and the Dalton Cardiovascular Research Center. "However, we have identified another way to target cancer cells using APR-246 that attack breast tumor cells as well as antibodies that target the blood vessels that supply nutrients to tumors. Our lab tested whether a combination of APR-246 and helpful antibodies would control tumor development by simultaneously restoring p53 protein function and reducing the that supply cancer cells with nutrients." Hyder and his team chose a specific antibody, 2aG4, which has the ability to destroy blood vessels and prevent future growth.

In the human cell lines that were in vitro, or outside the body, researchers saw that APR-246 induced a significant amount of tumor cell death. Then, the team tested the with APR-246/2aG4 in mice that had cancerous tumors. Tumor growth was more effectively suppressed by the combination treatment than by either agent alone. In some cases, the therapy completely eliminated cancerous tumors. Additionally, the researchers found that the combination therapy more effectively induced cancer cell death and dramatically reduced the density of blood vessels, which serve as a major route for metastasis.

"APR-246, the drug currently in human clinical trial, is showing very promising results," Hyder said. "Based on our findings, we can show that breast growth might effectively be controlled by simultaneously targeting the and the blood vessels that supply cancer cells through a combination therapy."

The early-stage results of this research are promising. If additional studies are successful within the next few years, these compounds may be tested in human clinical trials with the hope of developing new treatments for breast and other cancers.

This research highlights the power of translational precision medicine and the promise of the proposed Translational Precision Medicine Complex (TPMC) at the University of Missouri. The TPMC will bring together industry partners, multiple schools and colleges on campus, and the federal and state government to enable precision and personalized medicine. Scientific advancements made at MU will be effectively translated into new drugs, devices and treatments that deliver customized patient care based on an individual's genes, environment and lifestyle, ultimately improving health and well-being of people.

The study, "A combination of p53-activating APR-246 and phosphatidylserine-targeting antibody potently inhibits in hormone-dependent mutant p53-expressing breast xenografts," recently was published in Breast Cancer – Targets and Therapy.


Explore further

New cancer treatment targets both tumor cells and blood vessels

More information: Yayun Liang et al. A combination of p53-activating APR-246 and phosphatidylserine-targeting antibody potently inhibits tumor development in hormone-dependent mutant p53-expressing breast cancer xenografts, Breast Cancer: Targets and Therapy (2018). DOI: 10.2147/BCTT.S156285
Citation: Combination breast cancer therapy targets tumor cells and the blood vessels that feed them (2018, March 26) retrieved 24 September 2020 from https://medicalxpress.com/news/2018-03-combination-breast-cancer-therapy-tumor.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
9 shares

Feedback to editors

User comments