Src homology 2 domain-containing transforming protein C1 (Shc1) is a critical player in the transduction of mitogenic signaling cascades and is implicated in the regulation of numerous cellular processes, including proliferation, differentiation, and survival. As an adaptor protein, Shc1 functions by linking activated receptor tyrosine kinases (RTKs) with downstream effectors, thus facilitating the propagation of intracellular signals. The protein achieves this through its multiple domains, which allow for the simultaneous interaction with different signaling molecules. The expression of Shc1 is tightly controlled and can be upregulated by a variety of extracellular signals and chemical compounds, reflecting its dynamic role in cellular physiology. Understanding the factors that induce Shc1 expression is crucial for comprehending how cells respond to their environment and how they adjust their signaling networks in response to external stimuli.
Several chemical compounds have been identified to potentially induce the expression of Shc1. Estradiol, a naturally occurring hormone, can upregulate Shc1 by engaging estrogen receptors, which translocate to the nucleus and facilitate the transcription of estrogen-responsive genes. Similarly, dexamethasone, a synthetic glucocorticoid, can stimulate Shc1 expression by binding to glucocorticoid receptors, which then modulate the expression of glucocorticoid-responsive genes. On the other hand, retinoic acid, found in vitamin A, induces Shc1 through its interaction with retinoic acid receptors that bind to DNA at retinoic acid response elements and modulate gene expression. Natural compounds such as Epigallocatechin gallate (EGCG) found in green tea, and resveratrol, a polyphenol in grapes, can also increase Shc1 expression through their antioxidative properties, which may lead to the activation of various transcriptional pathways. Moreover, chemical agents like forskolin and Phorbol 12-myristate 13-acetate (PMA) can elevate Shc1 levels by stimulating cAMP and activating protein kinase C (PKC), respectively, indicating the diverse mechanisms through which Shc1 expression can be enhanced. These compounds exemplify the range of molecules that can signal through cellular membranes to the genome, ultimately leading to an upregulation of Shc1 protein levels and influencing the cellular signaling landscape.
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