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知母皂苷 AIII 是一种甾体皂苷,在体外和体内均对紫杉醇耐药细胞表现出抗肿瘤作用。

Timosaponin AIII, a steroidal saponin, exhibits anti-tumor effect on taxol-resistant cells in vitro and in vivo.

机构信息

Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China; Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research & Development, Liaoning Province, People's Republic of China.

Department of Natural Products Chemistry, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China; Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research & Development, Liaoning Province, People's Republic of China.

出版信息

Steroids. 2019 Jun;146:57-64. doi: 10.1016/j.steroids.2019.03.009. Epub 2019 Apr 2.

Abstract

Timosaponin AIII (TAIII), a steroidal saponin isolated from the rhizome of Anemarrhena asphodeloides, exerted cytotoxic effect in many cancer cell lines. However, the effect of TAIII on resistant tumor cancer cells was unclear. In this study, MTT assay showed that TAIII exhibited significant cytotoxicity against A549/Taxol and A2780/Taxol cells in vitro. Annexin V-FITC/PI staining revealed that TAIII induced apoptosis in A549/T and A2780/T cells. Furthermore, Western blot analysis demonstrated that TAIII inhibited the expressions of phosphatidylinositol 3-kinase (PI3K), protein kinase B (AKT), mammalian target of rapamycin (mTOR) as well as Ras, Raf, mitogen-activated protein kinase (MEPK), extracellular regulated protein kinases (ERK) in two taxol-resistant cancer cell lines. Besides, in vivo studies demonstrated that TAIII inhibited tumor growth in a nude mouse xenograft model. Additionally, TAIII (2.5 and 5 mg/kg) also down-regulated the protein expressions of PI3K/AKT/mTOR and Ras/Raf/MEK/ERK pathways in vivo. Taken together, these findings demonstrated that TAIII exhibited significant anti-tumor effect on taxol-resistant cells.

摘要

知母皂苷 AIII(TAIII)是从知母根茎中分离得到的一种甾体皂苷,在许多癌细胞系中表现出细胞毒性作用。然而,TAIII 对耐药肿瘤癌细胞的作用尚不清楚。在这项研究中,MTT 法检测表明 TAIII 在体外对 A549/Taxol 和 A2780/Taxol 细胞具有显著的细胞毒性作用。Annexin V-FITC/PI 染色显示 TAIII 诱导 A549/T 和 A2780/T 细胞凋亡。此外,Western blot 分析表明 TAIII 抑制了两种紫杉醇耐药癌细胞系中磷酸肌醇 3-激酶(PI3K)、蛋白激酶 B(AKT)、雷帕霉素靶蛋白(mTOR)以及 Ras、Raf、丝裂原活化蛋白激酶(MEK)、细胞外调节蛋白激酶(ERK)的表达。此外,体内研究表明 TAIII 抑制裸鼠异种移植模型中的肿瘤生长。此外,TAIII(2.5 和 5mg/kg)还下调了体内 PI3K/AKT/mTOR 和 Ras/Raf/MEK/ERK 通路的蛋白表达。综上所述,这些发现表明 TAIII 对紫杉醇耐药细胞表现出显著的抗肿瘤作用。

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