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-  2019 

Cancer-Associated Intermediate Conductance Ca2+-Activated K+ Channel KCa3.1

DOI: 10.3390/cancers11010109

Keywords: KCa3.1, intermediate conductance calcium-activated K+ channel, BK, big conductance Ca2+- and voltage-activated K+ channels, TRAM-34, (1-[(2-chlorophenyl) diphenylmethyl]-pyrazole, 1-EBIO, 1-Ethyl-1,3-dihydro-2H-benzimidazol-2-one, E2, 17β-estradiol

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Abstract:

Several tumor entities have been reported to overexpress KCa3.1 potassium channels due to epigenetic, transcriptional, or post-translational modifications. By modulating membrane potential, cell volume, or Ca2+ signaling, KCa3.1 has been proposed to exert pivotal oncogenic functions in tumorigenesis, malignant progression, metastasis, and therapy resistance. Moreover, KCa3.1 is expressed by tumor-promoting stroma cells such as fibroblasts and the tumor vasculature suggesting a role of KCa3.1 in the adaptation of the tumor microenvironment. Combined, this features KCa3.1 as a candidate target for innovative anti-cancer therapy. However, immune cells also express KCa3.1 thereby contributing to T cell activation. Thus, any strategy targeting KCa3.1 in anti-cancer therapy may also modulate anti-tumor immune activity and/or immunosuppression. The present review article highlights the potential of KCa3.1 as an anti-tumor target providing an overview of the current knowledge on its function in tumor pathogenesis with emphasis on vasculo- and angiogenesis as well as anti-cancer immune responses

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