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利用 siRNA 工具及其递送平台抑制顺铂耐药性:开创癌症化疗的新时代。

Employing siRNA tool and its delivery platforms in suppressing cisplatin resistance: Approaching to a new era of cancer chemotherapy.

机构信息

Department of Biology, Faculty of Science, Islamic Azad University, Science and Research Branch, Tehran, Iran.

Faculty of Veterinary Medicine, Kazerun Branch, Islamic Azad University, Kazerun, Iran.

出版信息

Life Sci. 2021 Jul 15;277:119430. doi: 10.1016/j.lfs.2021.119430. Epub 2021 Mar 28.

Abstract

Although chemotherapy is a first option in treatment of cancer patients, drug resistance has led to its failure, requiring strategies to overcome it. Cancer cells are capable of switching among molecular pathways to ensure their proliferation and metastasis, leading to their resistance to chemotherapy. The molecular pathways and mechanisms that are responsible for cancer progression and growth, can be negatively affected for providing chemosensitivity. Small interfering RNA (siRNA) is a powerful tool extensively applied in cancer therapy in both pre-clinical (in vitro and in vivo) and clinical studies because of its potential in suppressing tumor-promoting factors. As such oncogene pathways account for cisplatin (CP) resistance, their targeting by siRNA plays an important role in reversing chemoresistance. In the present review, application of siRNA for suppressing CP resistance is discussed. The first priority of using siRNA is sensitizing cancer cells to CP-mediated apoptosis via down-regulating survivin, ATG7, Bcl-2, Bcl-xl, and XIAP. The cancer stem cell properties and related molecular pathways including ID1, Oct-4 and nanog are inhibited by siRNA in CP sensitivity. Cell cycle arrest and enhanced accumulation of CP in cancer cells can be obtained using siRNA. In overcoming siRNA challenges such as off-targeting feature and degradation, carriers including nanoparticles and biological carriers have been applied. These carriers are important in enhancing cellular accumulation of siRNA, elevating gene silencing efficacy and reversing CP resistance.

摘要

虽然化疗是癌症患者治疗的首选方法,但药物耐药性导致其失败,需要采取策略来克服它。癌细胞能够在分子途径之间切换,以确保其增殖和转移,从而导致对化疗的耐药性。负责癌症进展和生长的分子途径和机制,可以通过提供化疗敏感性而受到负面影响。小干扰 RNA(siRNA)是一种强大的工具,由于其在抑制肿瘤促进因子方面的潜力,已广泛应用于临床前(体外和体内)和临床研究中的癌症治疗。由于这些致癌基因途径导致顺铂(CP)耐药,因此 siRNA 靶向这些途径在逆转化疗耐药性方面发挥着重要作用。在本综述中,讨论了 siRNA 在抑制 CP 耐药性中的应用。使用 siRNA 的首要任务是通过下调生存素、ATG7、Bcl-2、Bcl-xl 和 XIAP 来使癌细胞对 CP 介导的细胞凋亡敏感。siRNA 可抑制癌症干细胞特性和相关分子途径,包括 ID1、Oct-4 和 nanog,从而提高 CP 敏感性。siRNA 可使细胞周期停滞并增加 CP 在癌细胞中的积累。为了克服 siRNA 的挑战,如脱靶和降解,已经应用了包括纳米颗粒和生物载体在内的载体。这些载体在增强 siRNA 的细胞积累、提高基因沉默效果和逆转 CP 耐药性方面非常重要。

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