Mechanosensitive Steroid Hormone Signaling and Cell Fate
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Published on: April 14, 2017
Jason J Northey1,2, Valerie M Weaver1,2,3,4,5
1Department of Surgery, University of California, San Francisco, CA 94143, USA.
Abstract:
Mechanical forces collaborate across length scales to coordinate cell fate during development and the dynamic homeostasis of adult tissues. Similarly, steroid hormones interact with their nuclear and nonnuclear receptors to regulate diverse physiological processes necessary for the appropriate development and function of complex multicellular tissues. Aberrant steroid hormone action is associated with tumors originating in hormone-sensitive tissues and its disruption forms the basis of several therapeutic interventions. Prolonged perturbations to mechanical forces may further foster tumor initiation and the evolution of aggressive metastatic disease. Recent evidence suggests that steroid hormone and mechanical signaling intersect to direct cell fate during development and tumor progression. Potential mechanosensitive steroid hormone signaling pathways along with their molecular effectors will be discussed in this context.
Insights
Mechanical forces and steroid hormones coordinate cell fate in development and tissue homeostasis. Their signaling pathways intersect, influencing cell fate during development and cancer progression.
Area of Science:
- Cell biology
- Developmental biology
- Endocrinology
Background:
- Mechanical forces and steroid hormones are crucial for tissue development and homeostasis.
- Disrupted steroid hormone signaling is linked to hormone-sensitive tumors.
- Mechanical force alterations can promote tumor initiation and metastasis.
Purpose of the Study:
- To explore the intersection of mechanical and steroid hormone signaling in cell fate determination.
- To discuss potential mechanosensitive steroid hormone pathways and their effectors.
Main Methods:
- Literature review of recent evidence on mechanical and steroid hormone signaling.
- Discussion of molecular effectors and signaling pathways.
Main Results:
- Mechanical forces and steroid hormones collaborate to regulate cell fate.
- These signaling pathways intersect during development and tumor progression.
- Potential mechanosensitive pathways mediating these interactions are identified.
Conclusions:
- The interplay between mechanical forces and steroid hormones is critical for cell fate regulation.
- Understanding these intersections can inform therapeutic strategies for hormone-related diseases and cancer.
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