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
PURITAN MEDICAL

Download Mobile App




Search for Drugs to Treat Spinal Muscular Atrophy Pinpoints Likely Target Enzyme

By LabMedica International staff writers
Posted on 02 Mar 2016
Neurological disease researchers have identified a target for drugs to treat the hereditary childhood neurodegenerative disorder spinal muscular atrophy (SMA).

SMA is caused by a mutation in the SMN1 (survival motor neuron 1) gene. More...
SMN1 deficiency causes spinal motor neuron degeneration, which results in progressive muscle atrophy and death. The molecular mechanism underlying neurodegeneration in SMA is unknown, and no treatment is currently available to prevent neurodegeneration and reduce the burden of illness.

Investigators at the Texas Tech University Health Sciences Center (El Paso, USA) worked with neuron cultures and mouse models of SMA while searching for possible drug targets that would correct the neurological damage caused by the disorder.

They reported in the December 15, 2015, issue of the journal Human Molecular Genetics that they had identified the c-Jun NH2-terminal kinase (JNK) signaling pathway as being responsible for neurodegeneration in SMA. The neuron-specific protein isoform Jnk3 was required for the neuron degeneration caused by SMN1 deficiency, while lack of Jnk3 reduced degeneration of cultured neurons caused by low levels of SMN1. Genetic inhibition of the JNK pathway in JNK3 knockout mice resulted in relief of SMA symptoms. Jnk3 deficiency prevented the loss of spinal cord motor neurons, reduced muscle degeneration, improved muscle fiber thickness and muscle growth, improved motor function and overall growth and increased lifespan of mice with SMA.

"So far, spinal muscular atrophy research has focused on targeting the genetic mutation to prevent degeneration of spinal motor neurons, but it has not been successful because of challenges associated with gene therapy," said senior author Dr. Laxman Gangwani, associate professor of neurosciences at Texas Tech University Health Sciences Center. "This is the first study done that identifies a target, Jnk3, that is independent of the genetic mutation of spinal muscular atrophy for novel therapeutic development.

"Jnk3 represents a promising new avenue of research for clinical advances in developing a treatment," said Dr. Gangwani. "We saw less muscle degeneration, more muscle growth and better muscle strength, and improvement in overall movement. What were more striking were a four-fold reduction in initial mortality period and a two-fold increase in total lifespan."

Related Links:

Texas Tech University Health Sciences Center



Gold Member
Troponin T QC
Troponin T Quality Control
Serological Pipet Controller
PIPETBOY GENIUS
New
Silver Member
Quality Control Material
NATtrol Chlamydia trachomatis Positive Control
New
Silver Member
Quality Control Material
Multichem ID-B
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








DIASOURCE (A Biovendor Company)

Channels

Hematology

view channel
Image: CitoCBC is the world first cartridge-based CBC to be granted CLIA Waived status by FDA (Photo courtesy of CytoChip)

Disposable Cartridge-Based Test Delivers Rapid and Accurate CBC Results

Complete Blood Count (CBC) is one of the most commonly ordered lab tests, crucial for diagnosing diseases, monitoring therapies, and conducting routine health screenings. However, more than 90% of physician... Read more

Immunology

view channel
Image: An “evolutionary” approach to treating metastatic breast cancer could allow therapy choices to be adapted as patients’ cancer changes (Photo courtesy of 123RF)

Evolutionary Clinical Trial to Identify Novel Biomarker-Driven Therapies for Metastatic Breast Cancer

Metastatic breast cancer, which occurs when cancer spreads from the breast to other parts of the body, is one of the most difficult cancers to treat. Nearly 90% of patients with metastatic cancer will... Read more

Pathology

view channel
Image: A real-time trial has shown that AI could speed cancer care (Photo courtesy of Campanella, et al., Nature Medicine)

AI Accurately Predicts Genetic Mutations from Routine Pathology Slides for Faster Cancer Care

Current cancer treatment decisions are often guided by genetic testing, which can be expensive, time-consuming, and not always available at leading hospitals. For patients with lung adenocarcinoma, a critical... Read more

Technology

view channel
Image: Researchers Dr. Lee Eun Sook and Dr. Lee Jinhyung examine the imprinting equipment used for nanodisk synthesis (Photo courtesy of KRISS)

Multifunctional Nanomaterial Simultaneously Performs Cancer Diagnosis, Treatment, and Immune Activation

Cancer treatments, including surgery, radiation therapy, and chemotherapy, have significant limitations. These treatments not only target cancerous areas but also damage healthy tissues, causing side effects... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.