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Enhanced Selective Cytotoxicity in Pancreatic Cancer Cells Using EGF-Conjugated' Liposome-EncapsUlated Curcumin

机译:使用EGF缀合的'脂质体包封的姜黄素增强胰腺癌细胞中的选择性细胞毒性

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Pancreatic cancer is one of the most lethal cancers. Overexpression of epidermal growth factor receptor (EGFR) on the cell surface significantly enhances the tumor resistance, which makes the treatment even more challenging. Curcumin, a polyphenol found in turmeric (Curcumin longa), has been demonstrated to inhibit the growth, metastasis, and invasion of cancer cells via the EGFR signaling pathways. Our purpose is to develop an epidermal growth factor (EGF)-conjugated liposome-encapsulated curcumin (EGF-LP-Cur) to target the EGFR. As a result, the prepared liposomal EGF-LP-Cur had spherical vesicles with diameters of around 120 ran and contained high concentrations of curcumin and controlled concentrations of EGF. It was demonstrated to be stable in term of size and zeta potential within 21 days. The targeted formulation produced a significant increase of cytotoxicity on EGFR-overexpressed human pancreatic cancer cells as compared to the non-targeted one (p < 0.05). This is a promising candidate for the drug development in the treatment of pancreatic cancer, which remains challenging.
机译:胰腺癌是最致命的癌症之一。细胞表面上表皮生长因子受体(EGFR)的过度表达显着提高了肿瘤抗性,这使得治疗更具挑战性。已经证明姜黄素是在姜黄(姜黄Longa)中发现的多酚,以通过EGFR信号通路抑制癌细胞的生长,转移和侵袭。我们的目的是开发表皮生长因子(EGF) - 将脂质体包封的姜黄素(EGF-LP CUR)靶向靶向EGFR。结果,制备的脂质体EGF-LP CUR具有直径约120RAN的球形囊泡,并且包含高浓度的姜黄素和受控浓度的EGF。在21天内,它被证明在规模和Zeta电位期间稳定。与非靶向α相比,靶向制剂在EGFR过表达的人胰腺癌细胞上产生了显着增加(P <0.05)。这是治疗胰腺癌的药物发育的有希望的候选者,这仍然具有挑战性。

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