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

Download Mobile App




Critical Gene Altered in Numerous Fibroadenoma Patients

By LabMedica International staff writers
Posted on 13 Aug 2014
Advanced DNA sequencing technologies have been used to identify a critical gene that was repeatedly disrupted in nearly 60% of fibroadenoma cases.

Frequently discovered in clinical workups for breast cancer diagnosis and during routine breast cancer screening, clinicians often face the challenge of distinguishing fibroadenomas from breast cancer.

A multidisciplinary team of scientists from the National Cancer Center Singapore (Singapore) and their colleagues studies a total of 98 fibroadenoma tumors of which 12 were from fresh-frozen tumors and a further 86 were from archival formalin-fixed paraffin-embedded (FFPE) samples. More...
Tumors and whole blood were obtained from patients undergoing surgical excision of fibroadenoma.

The team used a variety of molecular techniques including a technique called laser capture microdissection (LCM). Fresh-frozen fibroadenomas were embedded in optimal cutting temperature (OCT) compound and 8 μm-thick sections were cut using a microtome cryostat. Stained slides were then loaded onto the laser capture microscope stage. The ArcturusXT Laser Capture Microdissection (LCM) System and a Capsure Macro LCM cap (Life Technologies, Grand Island, NY, USA) were then placed automatically over the chosen area of the tissue.

By analyzing all the protein-coding genes in a panel of fibroadenomas from the patients, the team identified frequent mutations in a gene called Mediator Complex Subunit 12 (MED12) in a remarkable 60% of fibroadenomas. Like most breast tumors including breast cancers, fibroadenomas consist of a mixed population of different cell types, called epithelial cells and stromal cells. However, unlike breast cancers where the genetic abnormalities arise from the epithelial cells, the scientists showed that the pivotal MED12 mutations in fibroadenomas are found in the stromal cells using the LCM technique.

Patrick Tan, MD, PhD, a professor and a lead author of the study said, “It is amazing that these common breast tumors can be caused by such a precise disruption in a single gene. Our findings show that even common diseases can have a very exact genetic basis. Importantly, now that we know the cause of fibroadenoma, this study can have many potential applications. For example, measuring the MED12 gene in breast lumps may help clinicians to distinguish fibroadenomas from other types of breast cancer. Drugs targeting the MED12 pathway may also be useful in patients with multiple and recurrent fibroadenomas as this could help patients avoid surgery and relieve anxiety.” The study was published on July 20, 2014, in the journal Nature Genetics.

Related Links:

National Cancer Center Singapore
Life Technologies, Grand Island



Gold Member
Automatic Hematology Analyzer
DH-800 Series
Collection and Transport System
PurSafe Plus®
Sample Transportation System
Tempus1800 Necto
Laboratory Software
ArtelWare
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

Hematology

view channel
Image: New evidence shows viscoelastic testing can improve assessment of blood clotting during postpartum hemorrhage (Photo courtesy of 123RF)

Viscoelastic Testing Could Improve Treatment of Maternal Hemorrhage

Postpartum hemorrhage, severe bleeding after childbirth, remains one of the leading causes of maternal mortality worldwide, yet many of these deaths are preventable. Standard care can be hindered by delays... Read more

Immunology

view channel
Image: When assessing the same lung biopsy sample, research shows that only 18% of pathologists will agree on a TCMR diagnosis (Photo courtesy of Thermo Fisher)

Molecular Microscope Diagnostic System Assesses Lung Transplant Rejection

Lung transplant recipients face a significant risk of rejection and often require routine biopsies to monitor graft health, yet assessing the same biopsy sample can be highly inconsistent among pathologists.... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.