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Turning Cancer Friend Into Cancer Foe

Date:
October 10, 2008
Source:
Burnham Institute
Summary:
Scientists have created a peptide that binds to Bcl-2, a protein that protects cancer cells from programmed cell death, and converts it into a cancer cell killer. The research may lead to new cancer treatments.
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Scientists have created a peptide that binds to Bcl-2, a protein that protects cancer cells from programmed cell death, and converts it into a cancer cell killer.

The Bcl-2 protein has long been implicated in protecting cancer cells from apoptosis (programmed cell death), the process that usually keeps cancer cells in check. This peptide (called NuBCP-9) and its enantiomer (mirror-image molecule) work on Bcl-2 like a molecular switch, converting it into a pro-apoptotic protein, and inducing cell death in cancer cells.

“Our results provide insight into Bcl-2 conversion and identify a new direction for Bcl-2-based drug leads and cancer drug development,” said Xiao-kun Zhang, Ph.D. of the Burnham Institute for Medical Research, who co-authored the paper with Arnold Satterthwait, Ph.D. and others.

The NuBCP-9 peptide was created from Nur77, a potent pro-apoptotic protein. Nur77 often moves from the nucleus to mitochondria, in response to different death signals, where it binds to Bcl-2, changing its shape and function.

The research, which was published in the October 7 edition of Cancer Cell, may lead to new cancer treatments.


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Materials provided by Burnham Institute. Note: Content may be edited for style and length.


Cite This Page:

Burnham Institute. "Turning Cancer Friend Into Cancer Foe." ScienceDaily. ScienceDaily, 10 October 2008. <www.sciencedaily.com/releases/2008/10/081007120429.htm>.
Burnham Institute. (2008, October 10). Turning Cancer Friend Into Cancer Foe. ScienceDaily. Retrieved April 19, 2024 from www.sciencedaily.com/releases/2008/10/081007120429.htm
Burnham Institute. "Turning Cancer Friend Into Cancer Foe." ScienceDaily. www.sciencedaily.com/releases/2008/10/081007120429.htm (accessed April 19, 2024).

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