• HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
Wednesday, July 30, 2025
BIOENGINEER.ORG
No Result
View All Result
  • Login
  • HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
        • Lecturer
        • PhD Studentship
        • Postdoc
        • Research Assistant
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
  • HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
        • Lecturer
        • PhD Studentship
        • Postdoc
        • Research Assistant
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
No Result
View All Result
Bioengineer.org
No Result
View All Result
Home NEWS Science News Cancer

Famous cancer-fighting gene also protects against birth defects

Bioengineer by Bioengineer
April 9, 2019
in Cancer
Reading Time: 2 mins read
0
ADVERTISEMENT
Share on FacebookShare on TwitterShare on LinkedinShare on RedditShare on Telegram

p53 influences an important molecular process specific to females that is necessary for the brain and spinal cord to form

Credit: Ms Etsuko Uno and Dr Drew Berry, Walter and Eliza Hall Institute

New research has revealed how the famous tumour suppressor gene p53 is surprisingly critical for development of the neural tube in female embryos. This is important because healthy development of the neural tube is needed for the brain and the spinal cord to form properly.

The study, published today in the journal Cell Reports, explained p53’s involvement in a molecular process specific to females called ‘X chromosome inactivation’. The new findings helped to clarify why females are significantly more likely than males to be born with neural tube birth defects, such as spina bifida.

The research, led by Associate Professor Anne Voss, Professor Andreas Strasser and Associate Professor Marnie Blewitt from the Walter and Eliza Hall Institute of Medical Research, was performed in collaboration with researchers at the Peter MacCallum Cancer Centre.

The collaborative teams were surprised to discover how the gene p53, famous throughout scientific literature and history for its role in protecting us from cancer, also played a pivotal role in healthy neural tube development.

Professor Strasser said the research showed how p53 influenced the function of genes required for fostering the production of healthy neural tube cells in the female embryo.

“Healthy development is a very precise and precariously balanced process. p53 helps with this balancing act in the female embryo by producing normal levels of Xist RNA, part of an intricate molecular process important for X chromosome inactivation. This in turn leads to healthy neural tube development. Simply put, healthy neural tube development in the female embryo requires the help of p53,” he said.

Associate Professor Voss said the study confirmed a long-standing theory that females had an additional risk factor for neural tube defects and that a breakdown in the associated X chromosome inactivation process could help to explain why females were more likely than males to have neural tube-related birth defects.

“Females have two copies of the ‘X’ sex chromosome, while males only have one copy. In order to maintain health in females, one of these X chromosomes must be inactivated in cells early on during development. If this inactivation does not occur efficiently, the neural tube will not form properly. Previous research indicated that p53 played a role in normal neural tube development, but it had never been shown exactly how this worked until now,” she said.

Professor Strasser said the findings were a terrific example of how strong collaborative research could drive remarkable discoveries. “Together our teams have surfaced exciting new information about a gene that has been intensely studied and is very well understood,” he said.

###

Media Contact
Arunee Wilson
[email protected]

Tags: BiologycancerCell BiologyDevelopmental/Reproductive BiologyGeneticsMedicine/Health
Share12Tweet7Share2ShareShareShare1

Related Posts

Cracking the Code of Cancer Drug Resistance

Cracking the Code of Cancer Drug Resistance

July 29, 2025
EMT and Cancer: Essential Insights for Clinicians

EMT and Cancer: Essential Insights for Clinicians

July 26, 2025

Vepdegestrant Outperforms Fulvestrant in Mutant ER+ Breast Cancer

July 26, 2025

Expanding MET’s Therapeutic Role in NSCLC and Beyond

July 26, 2025
Please login to join discussion

POPULAR NEWS

  • Blind to the Burn

    Overlooked Dangers: Debunking Common Myths About Skin Cancer Risk in the U.S.

    57 shares
    Share 23 Tweet 14
  • USF Research Unveils AI Technology for Detecting Early PTSD Indicators in Youth Through Facial Analysis

    42 shares
    Share 17 Tweet 11
  • Dr. Miriam Merad Honored with French Knighthood for Groundbreaking Contributions to Science and Medicine

    45 shares
    Share 18 Tweet 11
  • Engineered Cellular Communication Enhances CAR-T Therapy Effectiveness Against Glioblastoma

    35 shares
    Share 14 Tweet 9

About

We bring you the latest biotechnology news from best research centers and universities around the world. Check our website.

Follow us

Recent News

Merbecovirus S2 Vaccines Trigger Cross-Reactive MERS Protection

Cracking the Code of Cancer Drug Resistance

Peptidoglycan Links Prevent Lysis in Gram-Negative Bacteria

  • Contact Us

Bioengineer.org © Copyright 2023 All Rights Reserved.

Welcome Back!

Login to your account below

Forgotten Password?

Retrieve your password

Please enter your username or email address to reset your password.

Log In
No Result
View All Result
  • Homepages
    • Home Page 1
    • Home Page 2
  • News
  • National
  • Business
  • Health
  • Lifestyle
  • Science

Bioengineer.org © Copyright 2023 All Rights Reserved.