'Cooking' cancer cells with light, nanotechnology and biomolecules

19 June 2008

Researchers at the University of Texas, Dallas and University of Texas, Southwestern Medical Center, are testing new ways to kill cancer cells selectively by attaching cancer-seeking antibodies to tiny carbon tubes that heat up when exposed to near-infrared light. The biological molecules, called monoclonal antibodies, can work alone or can be attached to powerful anti-cancer drugs, radionuclides or toxins, to deliver a deadly payload to cancer cells.

The experiments conducted by biomedical scientists at these institutions have been described in a study available online and in an upcoming print issue of Proceedings of the National Academy of Sciences.

In this study, the researchers used monoclonal antibodies that targeted specific sites on lymphoma cells to coat tiny structures called carbon nanotubes. In cultures of cancerous lymphoma cells, the antibody-coated nanotubes attached themselves to the cells' surfaces. When these cells were exposed to near-infrared light, the nanotubes heated up, generating enough heat to essentially "cook" the cells and kill them.

Carbon nanotubes are very small cylinders of graphite carbon that heat up when exposed to near-infrared light. This is the same type of light, invisible to the human eye, which is used in TV remote controls to switch channels and is detected by night-vision goggles. It can penetrate human tissue up to about 1½ inches.

"Using near-infrared light for the induction of hyperthermia is particularly attractive because living tissues do not strongly absorb radiation in this range," said Dr. Ellen Vitetta, director of the Cancer Immunobiology Center at UT Southwestern and senior author of the study. "Once the carbon nanotubes have bound to the tumor cells, an external source of near-infrared light can be used to safely penetrate normal tissues and kill the tumor cells.

"Demonstrating this specific killing was the objective of this study. We have worked with targeted therapies for many years, and even when this degree of specificity can be demonstrated in a laboratory dish, there are many hurdles to translating these new therapies into clinical studies. We're just beginning to test this in mice, and although there is no guarantee it will work, we are optimistic."