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Anticancer potential of Salvia miltiorrhiza and its tanshinones: an efficacy perspective

机译:丹参及其丹参酮的抗癌潜力:疗效观察

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Salvia miltiorrhiza Bunge (Danshen in Chinese or Tanshen in Anglicized literature) is a well-known Traditional Chinese Medicine herbal remedy for treating cardiovascular- and cerebrovascular-related disorders. To date, >40 hydrophorbic tanshinones and structurally related compounds have been isolated from the Danshen root, as have some 50 hydrophilic phenolics and other minor components. In the past 2 decades, a large quantity of literature has reported inhibitory activities of tanshinones against cancers of various organ sites in cell culture models, and in some cases with efficacy confirmation in preclinical animal cancer models. This study follows up on a 2012 review we published on the sources, pharmacokinetics, and anticancer activities of tanshinones. Here, we update on the recent progress in understanding the anticancer potential of tanshinones and derivatives and critically assess merits of these entities for future research and development. Overall, potency data from in vivo efficacy assessment experiments in preclinical models varied from nil for chemoprevention of a prostate carcinogenesis model to strong inhibition of some xenograft or allograft models. Lack of uniformity of excipients, doses, and routes of administration aside, we caution that the reviewed data should be appreciated in balance of publication bias exemplified by our own data from primary carcinogenesis study and false positivity. Novel formulations and chemical modifications had been made to improve the poor solubility and bioavailability of tanshinones. Human clinical studies so far dealt with case reports of tanshinone IIA use and small-scale trials on Danshen-containing formulas with chemotherapy for cancers of multiple organ sites in People’s Republic of China. Available human data are not sufficient for supporting any anticancer indication of tanshinones.
机译:丹参(丹参或英语中的丹参)是治疗心血管和脑血管相关疾病的著名中药草药。迄今为止,已从丹参根中分离出40多种疏水性丹参酮和与结构相关的化合物,以及约50种亲水性酚类化合物和其他次要成分。在过去的二十年中,大量文献报道了丹参酮对细胞培养模型中各种器官部位的癌症具有抑制作用,在某些情况下,在临床前动物癌症模型中具有疗效证实。这项研究是我们在2012年发表的关于丹参酮的来源,药代动力学和抗癌活性的综述之后的。在这里,我们将介绍了解丹参酮及其衍生物的抗癌潜力的最新进展,并严格评估这些实体的优点,以供将来研究和开发。总体而言,临床前模型中体内功效评估实验的效价数据从零化学预防前列腺癌模型到强烈抑制某些异种移植或同种移植模型不等。除了赋形剂,剂量和给药途径的缺乏一致性外,我们提醒您应结合我们从原发癌变研究和假阳性中得到的数据来证明发表偏见的平衡,以评价所审查的数据。为了改善丹参酮的不良溶解性和生物利用度,已经进行了新的制剂和化学修饰。迄今为止,人类临床研究涉及使用丹参酮IIA的病例报告以及含丹参配方的化学疗法在中国多个器官部位的癌症中的小规模试验。现有的人类数据不足以支持丹参酮的任何抗癌指征。

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