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Published on: September 6, 2024
An Update on Src Family of Nonreceptor Tyrosine Kinases Biology
1Experimental Dermatology and Skin Biology Group, Ramón y Cajal Institute for Health Research (IRYCIS), Ramón y Cajal University Hospital, Colmenar Viejo Rd. Km 9,100, 28034 Madrid, Spain; Bionanotechnology Lab, Universidad Bernardo O´Higgins, General Gana 1780, 8370854 Santiago, Chile.
Abstract:
The members of the Src family of nonreceptor tyrosine kinases (SFKs) are implicated in multiple signaling processes that regulate key cellular functions, including proliferation, migration, differentiation, and survival. SFKs are activated by a large number of receptors for growth factors, cytokines, steroid hormones, G protein-coupled receptors, and also by adhesion proteins and other signaling partners. Through their common modular kinase an adapter protein domains, SFKs critically contribute to diversify different signal inputs, weaving a complex and dynamic network of cellular responses. Not surprisingly, SFKs are involved in embryo development and in the maintenance of different adult tissues and organs. Conversely, dysfunction of SFKs is associated with different pathologies, including cancer. Despite the continuous research in the field, several aspects of SFKs regulation and function are still not well defined and new roles for these proteins are steadily reported. The aim of this review is to provide an update on the major regulatory mechanisms of SFKs activity, including the emerging redox-dependent pathway. We have also focused on the functional implications of SFKs in Prolactin signaling and breast cancer development, two increasingly important aspects of SFKs biology. Finally, we briefly revisited the role of SFKs during embryo development and provide insights on the involvement of these proteins in the regulation of embryonic, somatic, and breast cancer stem cells.
Insights
Src family kinases (SFKs) regulate cell functions and are vital in development and tissue maintenance. This review updates SFK regulation, including redox pathways, and their roles in prolactin signaling, breast cancer, and stem cell biology.
Area of Science:
- Cellular Biology
- Molecular Biology
- Biochemistry
Background:
- Src family kinases (SFKs) are crucial nonreceptor tyrosine kinases involved in diverse cellular processes like proliferation, migration, differentiation, and survival.
- SFKs integrate signals from various receptors, including growth factors, hormones, and adhesion proteins, contributing to complex cellular signaling networks.
- Dysregulation of SFKs is linked to various pathologies, notably cancer, highlighting their importance in health and disease.
Purpose of the Study:
- To provide an updated overview of the major regulatory mechanisms governing SFK activity.
- To explore the emerging role of redox-dependent pathways in SFK regulation.
- To examine the functional implications of SFKs in prolactin signaling, breast cancer development, and stem cell regulation.
Main Methods:
- Literature review and synthesis of existing research on SFK regulation and function.
- Analysis of studies investigating SFK involvement in specific signaling pathways (e.g., prolactin signaling).
- Review of research on SFK roles in embryonic, somatic, and cancer stem cells.
Main Results:
- SFKs are regulated by multiple mechanisms, with redox-dependent pathways emerging as a significant area of study.
- SFKs play a critical role in prolactin signaling and are implicated in the development and progression of breast cancer.
- SFKs are involved in the regulation of stem cell populations, including embryonic, somatic, and breast cancer stem cells.
Conclusions:
- SFKs are central regulators of cellular functions, with their dysregulation contributing to diseases like cancer.
- Understanding SFK regulation, particularly redox-dependent mechanisms, is crucial for therapeutic development.
- SFKs have significant implications in stem cell biology and cancer, warranting further investigation.
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