We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Study Finds Five New Genetic Risk Loci for Endometrial Cancer

By LabMedica International staff writers
Posted on 16 May 2016
Genome-wide association studies (GWAS) have revealed five previously unknown risk loci for endometrial cancer.

Endometrial cancer is the third most common cause of death from women's cancers, behind ovarian and cervical cancer. More...
It is more common in the developed world and is the most common cancer of the female reproductive tract in developed countries. Rates of endometrial cancer have risen in a number of countries, and this is believed to be due to the increasing number of elderly people and increasing rates of obesity.

In a study designed to identify genetic risk indicators for endometrial cancer, investigators at the University of Cambridge (United Kingdom) and QIMR Berghofer Medical Research Institute (Brisbane, Australia) conducted a meta-analysis of three endometrial cancer genome-wide association studies and two follow-up phases totaling 7,737 endometrial cancer cases and 37,144 controls of European ancestry.

Results revealed five new risk loci of genome-wide significance. They also identified an allele that was protective in endometrial cancer by suppressing gene expression in vitro, suggesting that regulation of the expression of KLF5 (Krueppel-like factor 5), a gene linked to uterine development, was implicated in tumor development.

Contributing author Dr. Deborah Thompson a senior research associate in genetic epidemiology at the University of Cambridge, said, "Our findings help us to paint a clearer picture of the genetic causes of endometrial cancer in women, particularly where there no strong family history of cancer. Prior to this study, we only knew of four regions of the genome in which a common genetic variant increases a woman's risk of endometrial cancer. In this study we have identified another five regions, bringing the total to nine. This finding doubles the number of known risk regions, and therefore makes an important contribution to our knowledge of the genetic drivers of endometrial cancer."

"As we develop a more comprehensive view of the genetic risk factors for endometrial cancer, we can start to work out which genes could potentially be targeted with new treatments down the track," said senior author Dr. Amanda Spurdle, group leader in molecular cancer epidemiology at QIMR Berghofer Medical Research Institute. "In particular, we can start looking into whether there are drugs that are already approved and available for use that can be used to target those genes."

The study was published in the May 2, 2016, online edition of the journal Nature Genetics.

Related Links:
University of Cambridge
QIMR Berghofer Medical Research Institute


Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Neonatal Heel Incision Device
Tenderfoot
CMV CLIA Diagnostic
CLIA CMV IgA Screen Group
POC Immunoassay Analyzer
Procise DX
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image: Lead author Professor Chamindie Punyadeera. (Image Credit: Griffith University)

Breath Analysis Shows Promise for Distinguishing Cancerous from Benign Lung Nodules

Lung nodules are frequently detected during imaging, but distinguishing malignant from benign findings can require invasive procedures. Some patients undergo biopsies, bronchoscopy, or surgery before learning... Read more

Microbiology

view channel
Image: The clearance also broadens QIAstat-Dx\'s infectious disease testing menu in the U.S., which already includes panels for respiratory and gastrointestinal infections, as well as meningitis and encephalitis (Photo courtesy of Qiagen)

One-Hour Molecular Panel Expands Bloodstream Infection Testing for Gram-Negative Pathogens

Bloodstream infections can progress rapidly and lead to sepsis, organ failure, and death. In the United States, about 1.7 million adults develop sepsis each year, and at least 350,000 die during hospitalization... Read more

Industry

view channel
Image

Collaboration Combines AI Cognitive Assessment and RNA Blood Testing for Earlier Alzheimer’s Detection

Alzheimer’s disease is often identified only after substantial neurodegeneration, partly because current diagnostic pathways are fragmented and difficult to scale. As treatment shifts toward earlier intervention,... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.