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Novel Blocker of Onco SK3 Channels Derived from Scorpion Toxin Tamapin and Active against Migration of Cancer Cells

机译:Onco SK3通道的新型封锁器来自蝎子毒素茶蛋白,并激活癌细胞的迁移

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摘要

Peptide-based therapy against cancer is a field of great interest for biomedical developments. Since it was shown that SK3 channels promote cancer cell migration and metastatic development, we started using these channels as targets for the development of antimetastatic drugs. Particularly, tamapin (a peptide found in the venom of the scorpion Mesobuthus tamulus) is the most specific toxin against the SK2 channel currently known. Considering this fact, we designed diverse tamapin mutants based on three different hypotheses to discover a new potent molecule to block SK3 channels. We performed in vitro studies to evaluate this new toxin derivative inhibitor of cancer cell migration. Our results can be used to generate a new tamapin-based therapy against cancer cells that express SK3 channels.
机译:基于肽的癌症治疗是生物医学发展的极大兴趣的领域。 由于表明SK3通道促进癌细胞迁移和转移性发展,我们开始使用这些渠道作为抗致抗体药物的发展的目标。 特别是,Tamapin(在蝎子mesobuthus tamulus的毒液中发现的肽)是当前已知的SK2通道的最特异性毒素。 考虑到这一事实,我们基于三个不同的假设设计了多样化的Tamapin突变体,以发现新的有效分子来阻止SK3通道。 我们进行了体外研究,以评估这种新的毒素衍生物癌细胞迁移抑制剂。 我们的结果可用于生成基于新的Tamapin的疗法,针对表达SK3通道的癌细胞。

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