New Agent Might Control Breast-Cancer Growth and Spread

April 22, 2013
New Agent Might Control Breast Cancer Growth and Speed Carlo Croce

New Agent Might Control Breast Cancer Growth and Speed Flavia Picchoiri

Flavia Pichiorri, PhD

  • Altered levels of molecules called microRNA play an important role in many cancers, but efforts to treat cancer by altering those levels have been unsuccessful.
  • This study shows that a new type of drug might slow breast-cancer growth and spread by changing the levels of cancer-associated microRNAs.
  • The new agent might also reverse resistance to the breast-cancer drug fulvestrant and improve the effectiveness of other anti-cancer drugs.

COLUMBUS, Ohio – A new study led by researchers at The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC – James) suggests that an unusual experimental drug can reduce breast-cancer aggressiveness, reverse resistance to the drug fulvestrant and perhaps improve the effectiveness of other breast-cancer drugs.

The findings of the laboratory and animal study, published in the Journal of Experimental Medicine, suggest a new strategy for treating breast cancer, the researchers say.

The drug, called AS1411, belongs to a class of agents called G-rich aptamers. The agent works by blocking the cell’s production of molecules called microRNA, some types of which are associated with cancer. Specifically, the drug inhibits a protein called nucleolin that plays a critical role in the microRNA maturation process (see figure).

MicroRNA molecules help cells control the amount and kinds of proteins they make, and abnormal levels of certain microRNAs are a hallmark of many cancers.

“This study of the role of nucleolin in micro RNA regulation has clear clinical implications,” says principal investigator Dr. Carlo M. Croce, director of Ohio State’s Human Cancer Genetics program and a member of the OSUCCC – James Molecular Biology and Cancer Genetics program.

“It supports a novel treatment for breast cancer that reduces cancer aggressiveness and restores drug-sensitivity by inhibiting the processing of specific microRNAs that are highly expressed in cancers.”

First author Flavia Pichiorri, assistant professor of hematology, notes that nucleolin is a promising therapeutic target for microRNA modulation in cancer cells.

“To our knowledge, this is the first large study to show a clear association between nucleolin and specific microRNAs that are causally involved in cancer,” she says. “We also believe it is the first study to show that targeting nucleolin with a G-rich aptamer can control breast-cancer metastasis in an animal model through microRNA regulation.”

The study’s key technical findings include:

  • Nucleolin is present at abnormally high levels in breast cancer cells.
  • AS1411 reduces nucleolin levels and inhibits the processing of certain cancer-associated microRNAs, including miR-21, miR-103, miR-221 and miR-222, whose overexpression in breast cancer is associated with drug resistance and aggressiveness.
  • AS1411 affects breast-cancer-cell motility and invasiveness by reducing the expression of several genes targeted by nucleolin-related microRNAs (e.g., PTEN);
  • Impairing nucleolin in fulvestrant-resistant breast-cancer cells restores sensitivity to the drug, suggesting that agents targeting nucleolin can improve the effectiveness of conventional anti-cancer agents.

Funding from the NIH/National Cancer Institute (grants CA154200 and CA107106), the Kimmel Foundation and the Spielman Fund for Breast Cancer Research supported this research.

Other researchers involved in this study were Dario Palmieri, Jessica Consiglio, Jia You, Tiffany Talabere, Alessandro Lagana, Jingwen Guan, Pierluigi Gasparini, Veronica Balatti, Vincenzo Coppola, Craig C. Hofmeister, Guido Marcucci, John C. Byrd, Stefano Volinia, Charles L. Shapiro and Michael A. Freitas, The Ohio State University; Luciana De Luca of IRCCS Centro di Riferimento Oncologico della Basilicata, Italy; Alberto Rocci, University of Turin, Italy; Claudia Piovan, Istituto Nazionale Tumori, Italy; and Luciano Cascione, University of Catania, Italy.

The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute strives to create a cancer-free world by integrating scientific research with excellence in education and patient-centered care, a strategy that leads to better methods of prevention, detection and treatment. Ohio State is one of only 41 National Cancer Institute (NCI)-designated Comprehensive Cancer Centers and one of only seven centers funded by the NCI to conduct both phase I and phase II clinical trials. The NCI recently rated Ohio State’s cancer program as “exceptional,” the highest rating given by NCI survey teams. As the cancer program’s 210-bed adult patient-care component, The James is a “Top Hospital” as named by the Leapfrog Group and one of the top cancer hospitals in the nation as ranked by U.S.News & World Report.

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A high quality JPEG of Carlo M. Croce, MD, PhD, is available here.

A high quality JPEG of Flavia Pichiorri, PhD, is available here.

Contact: Darrell E. Ward, Wexner Medical Center Public Affairs and Media Relations, 614-293-3737, or Darrell.Ward@osumc.edu

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