Vitamin A Derivative Shown to Suppress Early Forms of Breast Cancer

A nutrient found in sweet potatoes and carrots may prove vital in combating breast cancer at its earliest stages.

Sandra Fernandez, PhD, an assistant research professor at Fox Chase Cancer Center (Philadelphia, PA, USA), presented the study's findings at the American Association of Cancer Research (AACR) 102nd annual meeting, held in Orlando (FL, USA) on April 2-6, 2011.

Retinoic acid, a derivative of vitamin A, could be a promising cancer therapy because it affects cell growth, proliferation, and survival. Although it is being evaluated in a number of clinical trials, so far its effectiveness at combating cancer has been inconsistent. However, Dr. Fernandez and her colleagues have now pinpointed critical characteristics of retinoic acid's manner of action--a potentially important step toward developing successful treatments for patients.

Retinoic acid binds to retinoic acid receptor beta (RAR-β), and it may be through this process that it can suppress tumors. A decrease in RAR-β levels in tumors is associated with cancer progression, and an increase is linked to positive responses to certain clinical interventions. It is thought that the activated receptor limits cell growth by regulating gene expression, but its underlying processes are not entirely understood.

To identify the specific conditions under which retinoic acid inhibits and even reverses the growth of abnormal masses in the breast, however, Dr. Fernandez developed a culture system consisting of four cell lines representing different phases of cancer: normal-like human breast cells; transformed cells (which give rise to solid masses upon exposure to carcinogens); invasive cells (which are capable of breaking through breast tissue barriers and spreading to other areas of the body); and tumor cells (which form when invasive cells are injected into the mammary fat pad of mice and show all of the characteristics of fully malignant breast cancer cells).

"We found that the RAR-β gene was active in the two earliest stages of cancer, but silenced in the final two stages,” said Dr. Fernandez. "These changes in gene activation were caused by a type of chemical modification called methylation, which involves the addition of a methyl group to DNA.”

In three-dimensional (3D) cultures containing a collagen matrix, normal-like cells formed tubules resembling a normal mammary gland, while the transformed cells also gave rise to solid masses. The cells that generated solid masses in collagen produced tubules when they received retinoic acid for 15 days. In comparison, invasive and tumor cells did not generate tubules in response to treatment with retinoic acid, even in combination with a drug that activates RAR-β by inhibiting DNA methylation.

The results suggest that retinoic acid can stop tumor progression early on, but not at later timepoints because the genetic changes related to cancer have become too severe. "There appears to be no way to revert the tumors with retinoic acid when they become too advanced,” Dr. Fernandez stated.

The study also revealed that the methylation status of RAR-β can act as a biomarker for the early detection of breast cancer. Moreover, drugs that reactivate this receptor by decreasing DNA methylation may help breast cancer patients. These agents are already being used to treat a specific type of leukemia, offering hope that it will also be approved to treat other diseases.

Related Links:
Fox Chase Cancer Center