-Press Release Number: PR-USC-06-1
-Source: University of Southern California
-Date issued: August 31, 2006
-Contact: Carl Marziali, +1 213-740-4751, marziali@usc.edu

Cell Struggle Against Tumor Documented

X-ray data portray struggle between pro- and anti-tumor proteins

If anything in cancer biology can be likened to a cage match, this is it: the battle inside the cell walls between LTag, "The Most Amazing Molecule in the Universe," and p53, "The Guardian of the Genome."

By the painstaking use of X-ray crystallography to track motion in very large molecules, a University of Southern California-led research group has taken a first look at the life-or-death struggle of a cancer-causing protein – LTag – and a key tumor suppressor – p53.

Each villainous LTag (short for large T antigen) single-handedly ties up a tag-team of six p53 molecules, inhibiting their tumor-suppressant role, the researchers report in the Sept. 1 issue of Genes & Development.

Undeterred, the p53 fight back by preventing replication of the virus that produces LTag, known as an oncoprotein for its function in cancer growth.

The champion depends on which side is stronger and healthier.

"If you have a lot of functional p53, you can override large T antigen," said lead researcher Xiaojiang Chen, professor in molecular and computational biology in the USC College of Letters, Arts and Sciences.

Sometimes called the "Guardian of the Genome," a damaged p53 can leave a cell almost defenseless.

"p53 is a very important tumor suppressor that's mutated in a vast majority of all cancers," said James Pipas, professor of biological sciences at the University of Pittsburgh.

It was Pipas who, after studying LTag for many years and marveling at its varied biological functions – including highly efficient tumor promotion – named it "The Most Amazing Molecule in the Universe" in one of his presentations.

Pipas called Chen's new study "a very important piece of work" that shows how a healthy cell's tumor defenses break down.

"Understanding exactly how this works is going to be a critical step toward our understanding of tumor genesis," he said.

This, in turn, may lead to new techniques for designing tumor-fighting drugs, Pipas added.

Chen's team was able to describe the interplay between LTag and p53 by crystallizing the complex of one LTag and six p53 molecules, totaling more than 50,000 atoms between them.

"It's quite a technical achievement, because these are fairly large proteins," Pipas said.

Chen said his study gave him new respect for LTag and its parent, Simian Virus 40. SV40 has long been used as a research tool to induce cancers in cell cultures.

"Somehow this virus knows how important p53 is, and has this oncoprotein (LTag) to target it by physically interacting with it and changing its conformation," Chen said.

If the virus succeeds, the result is a new tumor.

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Scientists from the University of Colorado and Argonne National Laboratory contributed to the study. Funding for the group's research came from the American Cancer Society.

The original news release can be found here.

[Note: Published in Genes & Development, 20:2373-2382, 2006; ISSN 0890-9369; Wayne Lilyestrom, Michael G. Klein, Rongguang Zhang, Andrzej Joachimiak and Xiaojiang S. Chen; "Crystal structure of SV40 large T-antigen bound to p53: interplay between a viral oncoprotein and a cellular tumor suppressor".

Native and Se-SAD data sets were collected at the Advanced Photon Source (Argonne National Laboratory), beamlines 19ID (SBC-CAT) and 14BMC (BioCARS). Argonne National Laboratory is funded by the U.S. Department of Energy's Office of Science.

The contents of all materials on lightsources.org are the sole responsibility of the authors of the materials and/or the facilities or institutions under whose auspices the materials were produced. -lightsources.org]

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