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Generation of Human Chimeric Antigen Receptor Regulatory T Cells
Published on: January 3, 2025
Dysfunction of the RET receptor in human cancer
M Santoro1, F Carlomagno, R M Melillo
1Dipartimento di Biologia e Patologia Cellulare e Molecolare, University Federico II, via S. Pansini 5, 80131 Naples, Italy. masantor@unina.it
Abstract:
RET is the receptor for glial-derived neurotrophic factor growth factors. It is a paradigm of a single gene that causes different types of human cancer when targeted by different genetic alterations. Like other receptor tyrosine kinases, once activated, RET recruits a variety of signaling molecules that mediate biological responses. Here we review data on the signaling pathways that lead to RET-mediated cell transformation and recent evidence that manipulation of RET holds promise for thyroid cancer treatment.
Insights
The RET receptor tyrosine kinase plays a key role in various human cancers. Targeting RET shows promise for effective thyroid cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- RET is a receptor tyrosine kinase crucial for neurotrophic factor signaling.
- Genetic alterations in RET can lead to diverse human cancers.
- RET activation initiates signaling cascades mediating cellular responses.
Purpose of the Study:
- To review signaling pathways involved in RET-mediated cell transformation.
- To highlight recent findings on RET's therapeutic potential in thyroid cancer.
Main Methods:
- Literature review of signaling pathways.
- Analysis of recent research on RET manipulation for cancer treatment.
Main Results:
- RET activation involves recruitment of signaling molecules.
- Specific genetic alterations of RET drive cell transformation.
- RET-targeted therapies demonstrate potential in preclinical models.
Conclusions:
- Understanding RET signaling is vital for cancer research.
- RET-targeted therapies offer a promising avenue for thyroid cancer treatment.
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