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JAMA Oncology Publishes Ambry's Results Detailing Genes Associated with Hereditary Breast and Ovarian Cancer

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The AmbryShare project produced innovative research that may identify more at-risk women

ALISO VIEJO, Calif. (PRWEB) August 16, 2018

Ambry Genetics Corporation ("Ambry"), a leader in high quality genetic testing, announced their results from the AmbryShare project were published today in JAMA Oncology, identifying new and confirming known hereditary breast and ovarian cancer candidate genes in the largest exome study ever conducted.

Every year hereditary breast cancer affects more than 20,000 women while hereditary ovarian cancer affects more than 6,000 women. Since the discovery of the BRCA1 and BRCA2 genes over 20 years ago, progress in establishing and confirming gene associations with hereditary breast and ovarian cancer has been slow. Major obstacles include limited access to large numbers of relevant samples, sequencing expertise, data sharing and financial resources. The understanding of the genetic component of these cancers has a direct impact on the ability to effectively identify patients susceptible to cancer.

Ambry's findings were based on a large-scale exome sequencing study of more than 11,400 hereditary breast and ovarian cancer patients from over 1200 clinics and nearly 4000 controls. The study confirmed that the genes PALB2, ATM and CHEK2 significantly increase breast cancer risk and identified the Lynch Syndrome susceptibility gene MSH6 as a candidate gene for breast cancer. In ovarian cancer, both ATM and MSH6 were found to be associated with increased risk along with the well characterized ovarian cancer predisposition genes RAD51C and TP53. Some previously reported associations were not confirmed in the study such as the association of the MRN complex genes and CDKN2A with increased breast or ovarian cancer risk. Likewise, results could not confirm a significant breast cancer association with the ovarian cancer susceptibility genes BRIP, RAD51C, RAD51D, MSH2 and PMS2.

The AmbryShare project highlights the value that large, high resolution, phenotype specific data sets bring to improving patient medical management. In addition to providing evidence for reported but unconfirmed candidate genes, the study was able to identify novel gene associations with breast and ovarian cancer. These results provide further insight into the genomic landscape of hereditary breast and ovarian cancer and will aid in improving the molecular diagnosis of these patients. AmbryShare was conceived to promote and inspire widespread data sharing, and inform comprehensive genetic testing and clinical practice. Learn more about AmbryShare here .

About Ambry
Ambry is both College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified. Ambry is a leader in high quality clinical genetic diagnostics and genetics software solutions, combining both to offer the most comprehensive testing menu in the industry. Ambry has established a reputation for sharing data while safeguarding patient privacy, unparalleled service, and responsibly applying new technologies to the clinical molecular diagnostics market. For more information about Ambry, visit ambrygen.com

Media Contact:
Dina Scaglione
Director, Marketing
949.457.4355
dscaglione(at)ambrygen.com

For the original version on PRWeb visit: https://www.prweb.com/releases/jama_oncology_publishes_ambrys_results_detailing_genes_associated_with_hereditary_breast_and_ovarian_cancer/prweb15697077.htm

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