Date published: 2025-11-2

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PRAMEF3 Activators

PRAMEF3, a member of the PRAME (Preferentially Expressed Antigen in Melanoma) family of genes, has piqued the interest of the scientific community due to its distinctive expression profile. PRAME family members are known as cancer-testis antigens because they are typically expressed in a variety of cancers while remaining quiescent in most normal tissues. PRAMEF3's function is not yet completely understood, but it is thought to play a role in the intricate biological processes associated with cell differentiation and proliferation. The regulation of PRAMEF3 expression is an area of active research, as it may provide insights into the molecular mechanisms that govern gene expression in both normal physiology and disease states.

The expression of PRAMEF3 can be influenced by a diverse array of chemical compounds, which can serve as activators by engaging with the cell's regulatory machinery. Compounds such as 5-Azacytidine and Trichostatin A, for instance, may induce expression by altering the epigenetic landscape; they're known to inhibit DNA methyltransferase and histone deacetylase, respectively, which can result in an open chromatin state conducive to gene transcription. Other activators, like retinoic acid and forskolin, may stimulate PRAMEF3 expression through receptor-mediated signaling pathways. Retinoic acid engages with its nuclear receptors, potentially increasing gene transcription, while forskolin elevates cAMP levels, activating protein kinase A and other downstream transcription factors. Additionally, compounds like doxorubicin and temozolomide could promote expression by inducing cellular stress responses, leading to the activation of signaling pathways that may include PRAMEF3 as a target. Natural compounds such as curcumin, epigallocatechin gallate, and sulforaphane are also considered potential activators due to their ability to modulate gene expression by affecting various signal transduction and epigenetic modulation pathways. It is through understanding the interaction of these compounds with cellular processes that researchers can elucidate the regulatory mechanisms controlling PRAMEF3 expression.

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