Product category:
Genomics
News Release from: Transgenomic
Edited by the Laboratorytalk Editorial
Team on 06 February 2007
Discovery by high-throughput mutation
analysis
Transgenomic files patents on novel somatic mutations in receptor tyrosine kinases important in angiogenesis; potential clinical markers for cancer prognosis and treatment, targets for new therapies
Transgenomic has filed patent applications directed to somatic mutations in the genes for five well-known receptor tyrosine kinases which may be useful as predictive biomarkers for various cancers and provide the potential for highly-targeted cancer therapies The genes harboring these newly described cancer mutations are KDR, FLT1, and FLT4, which encode receptors for different isoforms of vascular endothelial growth factor (VEGF); and PDGFRA and PDGFRB, which encode alpha and beta forms of the receptors for platelet-derived growth factor (PDGF)
This article was originally published on Laboratorytalk on 14 Jan 2002 at 8.00am (UK)
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These receptors are targets for some cancer drugs currently available, as well as a variety of experimental therapeutics in pre-clinical and clinical development phase.
Novel mutations in these receptors have been consistently found in a number of different cancer types including bladder, breast, colorectal, esophageal, gastric, glioma, head and neck, liver, lung, melanoma, ovarian, pancreatic, prostate, and uterine.
These patent applications are the first group in a series that Transgenomic intends to file protecting similar discoveries in other genes.
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The discoveries were made using HTMA (high-throughput mutation analysis), Transgenomic's proprietary mutation scanning strategy that integrates multiple processes and technologies for large-scale cancer genome screening that is accurate, robust and cost-effective.
"By implementing HTMA, we were able to conduct a thorough screening of the entire coding region of each gene amplified from over one-thousand tumour specimens.
"This revealed previously unknown mutations not only in the tyrosine kinase catalytic domains, but in other functional domains as well," explained Stan Lilleberg, chief scientist of translational and clinical research for Transgenomic and co-developer of HTMA.
"The intrinsic efficiency and sensitivity of this mutation screening strategy was achieved through a complete assessment and tactical refinement of each process involved, yielding a very powerful discovery tool - in the case of HTMA, the whole is definitely greater than the sum of its parts," added Dr Lilleberg, who will be presenting the results of some of these new discoveries at Oncogenomics 2007: Dissecting Cancer through Genomic Research, an AACR Special Conference being held in Phoenix, Arizona, January 31-February 3.
Key technologies critical for HTMA include Surveyor Nuclease, a double-stranded DNA mismatch cleaving endonuclease, and Wave HS, a high-sensitivity system for nucleic acid fragment analysis; both of which are also proprietary to Transgenomic.
"The majority of these somatic mutations would have been missed by any genomics laboratory using standard PCR methods, along with high-throughput DNA sequencing and automated data analysis".
"All of our procedures have been specifically optimised for somatic mutation detection, where tissue heterogeneity and low mutation loads present challenges for cancer genome screening in a discovery mode," stated Michael Nickerson, director of genomic research and biomarker discovery at Transgenomic and co-developer of HTMA.
Transgenomic's CEO, Craig Tuttle, notes: "These discoveries are the first in a series of patents that Transgenomic intends to file as was first disclosed in our discussion of 3rd quarter 2006 results.
"The new mutations have implications not only for assessing disease stage and prognosis, but are also useful to predict whether the cancer will be aggressive.
"They may also help determine which individuals will respond best to new drug therapies in clinical trials, and even to predict which drug or drug combinations will be most successful.
"These newly filed patent applications, and others soon to follow, showcase the unique capabilities of Transgenomic Laboratories discovery team and our proprietary technologies in the area of low level somatic mutation detection.
"We are actively looking for new partners to aid us in our efforts to bring these new discoveries to market so they will benefit patients.".
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