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Researchers Identify Genetic Mutation That May Alter Patients' Response
to Cancer Therapeutics


Recurring mutation found in breast, colorectal and ovarian cancers

07-04-2007

Phoenix, July 4, 2007--Researchers from Eli Lilly & Company and the
Phoenix-based Translational Genomics Research Institute (TGen) today
announced finding a novel recurring mutation of the gene AKT1 in breast,
colorectal and ovarian cancers. The altered form of AKT1 appears to
cause tumor cell proliferation and may play a role in making cells
resistant to certain types of therapies. The findings are reported in an
advance online publication (AOP) of the journal Nature.
The PI3-Kinase/AKT pathway is among the most commonly activated cellular
pathways in human cancers and members of this pathway are among the most
frequently targeted for new cancer drug discovery efforts. Activation of
this pathway results in cancer cell growth and cell survival. Although
AKT1 is central to pathway activation, its role in cancer has been that
of an intermediary between mutated upstream regulatory proteins and
downstream survival signaling proteins. This is the first evidence of
direct mutation of AKT1 in human cancer tumors: it was discovered in
clinical samples from cancer patients, yet has never been detected in
cancer cell lines.
More here:  Genetic Mutation and Cancer Therapy 
<http://www.arizonabiotech.com/2007/07/genetic-mutation-and-cancer-thera\
py.html>

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