Zfra Overrides WWOX in Suppressing the Progression of Neurodegeneration.
Yu-An ChenTsung-Yun LiuKuan-Yu WenChe-Yu HsuChun-I SzeNan-Shan ChangPublished in: International journal of molecular sciences (2024)
We reported that a 31-amino-acid Zfra protein (zinc finger-like protein that regulates apoptosis) blocks neurodegeneration and cancer growth. Zfra binds WW domain-containing oxidoreductase (WWOX) to both N - and C -termini, which leads to accelerated WWOX degradation. WWOX limits the progression of neurodegeneration such as Alzheimer's disease (AD) by binding tau and tau-hyperphosphorylating enzymes. Similarly, Zfra binds many protein targets and accelerates their degradation independently of ubiquitination. Furthermore, Zfra4-10 peptide strongly prevents the progression of AD-like symptoms in triple-transgenic (3xTg) mice during aging. Zfra4-10 peptide restores memory loss in 9-month-old 3xTg mice by blocking the aggregation of a protein cascade, including TPC6AΔ, TIAF1, and SH3GLB2, by causing aggregation of tau and amyloid β. Zfra4-10 also suppresses inflammatory NF-κB activation. Zfra-activated Hyal-2+ CD3- CD19- Z cells in the spleen, via Hyal-2/WWOX/Smad4 signaling, are potent in cancer suppression. In this perspective review, we provide mechanistic insights regarding how Zfra overrides WWOX to induce cancer suppression and retard AD progression via Z cells.
Keyphrases
- papillary thyroid
- amino acid
- cell cycle arrest
- induced apoptosis
- signaling pathway
- oxidative stress
- squamous cell
- cell death
- cerebrospinal fluid
- binding protein
- epithelial mesenchymal transition
- lymph node metastasis
- childhood cancer
- immune response
- squamous cell carcinoma
- high fat diet induced
- transforming growth factor
- skeletal muscle
- mouse model
- depressive symptoms
- nuclear factor
- metabolic syndrome
- adipose tissue
- lps induced
- oxide nanoparticles