Potential New Cancer Drug Target Identified

These findings were published in the June 8 issue of Molecular Cell by Dr. Hao Wu, a professor in the Department of Biochemistry of Weill Cornell, and her team.

Experts know that cancers spread in two separate ways — by the uncontrolled proliferation of cells, and by their refusal to undergo normal, healthy, programmed cell death, or "apoptosis."

In many cancers, dysfunction in a biochemical cascade called the NF-kappa B pathway causes tumor cells to sidestep apoptosis and become dangerously immortal.

"So, drug development aimed at short-circuiting NF-kappa B has become very hot in the past few years," Dr. Wu says.

Her team focused on a particular protein involved in the NF-kappa B pathway called the "X-linked inhibitor of apoptosis" (XIAP). Scientists had already discovered that XIAP thwarts the apoptotic impulse by putting the brakes on key enzymes called caspases. XIAP is also known to be highly active in cancer cells, but it is found in relatively low levels in healthy cells. How XIAP inhibits caspases is known, but how XIAP induces NF-kappa B activation is entirely unclear.

"We wondered if we could find out how XIAP induces the NF-kappa B pathway," explains lead researcher Dr. Miao Lu, a postdoctoral fellow of biochemistry at Weill Cornell.

In their experiments, the researchers used a variety of cutting-edge techniques, including X-ray crystallography, to track changes in the structure and activity of XIAP and the molecules it interacts with in cells.

"We discovered that XIAP interacts with the NF-kappa B cycle in two distinct ways," Dr. Wu says.

"It interacts with another key protein, called TAB1, and it also interacts on a structural level with itself — a process called dimerization," the researcher explains.

Since both of these two activities might be vulnerable to some kind of pharmaceutical interference or interruption, they present promising new targets for the development of anti-cancer drugs.

"This is really exciting," says Dr. Wu, "because it provides two new points of attack against cancer in a pathway that pharmacological researchers are already very familiar with. It's exactly this type of basic science discoveries that we hope — one day — will help lead to a cure."

This work was funded by the U.S. National Institutes of Health.

Co-researchers include Dr. Yu-Chih Lo, Su-Chan Lin and Yihua Huang — all of Weill Cornell Medical College; Dr. Young Jun Kang and Dr. Jiahuai Han, of The Scripps Research Institute, La Jolla, Calif; and Dr. David Myszka and Rebecca Rich of the University of Utah, Salt Lake City.