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Verbascoside: Identification Quantification and Potential Sensitization of Colorectal Cancer Cells to 5-FU by Targeting PI3K/AKT Pathway

机译:马鞭草苷:通过靶向PI3K / AKT途径对大肠癌细胞对5-FU的鉴定定量和潜在敏化

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摘要

Colorectal cancer (CRC) is the third most common cancer mortality worldwide. Although, 5-Fluorouracil (5-FU)-based chemotherapeutic regimens remain the mainstay for treatment of CRC, intrinsic and acquired resistance to 5-FU is the main reason for treatment failure and relapse. Adjunct or add-on therapy, therefore, should be thought of to enhance responsiveness to 5-FU. Verbascoside (VER) is a phenylethanoid glycoside ingredient present in many Plantago species and was widely used in traditional medicine. VER showed antiproliferative effects in many cancer types including CRC. In the present study, VER in Plantago seeds was identified using UPLC-MS/MS and quantified using newly developed and validated UPLC-DAD followed by investigating its potential sensitization of CRC cells to 5-FU in vitro. The potential impact on PI3K/AKT pathway was also investigated. A synergistic cytotoxic interaction between 5-FU and VER besides G1 cell cycle arrest were detected. Enhanced apoptosis mainly by affecting Bax and Bcl-2 and to a lesser extent Bcl-xL and p53 was also observed. Additionally, 5-FU combined to VER was capable of significantly reducing PI3K and p-AKT/total AKT ratio. Overall, these results suggest a potential role of VER as an adjuvant treatment to decrease the resistance of CRC cells to 5-FU possibly by targeting the PI3K/AKT pathway.
机译:大肠癌(CRC)是全球第三大最常见的癌症死亡率。尽管基于5-氟尿嘧啶(5-FU)的化疗方案仍然是CRC治疗的主要手段,但对5-FU的固有耐药性和获得性耐药是治疗失败和复发的主要原因。因此,应该考虑辅助或附加疗法以增强对5-FU的反应性。马鞭草苷(VER)是一种在许多车前草属物种中存在的苯乙醚类糖苷成分,已广泛用于传统医学中。 VER在包括CRC在内的许多癌症类型中均显示出抗增殖作用。在本研究中,使用UPLC-MS / MS鉴定了车前子种子中的VER,并使用新开发和验证的UPLC-DAD对其进行了定量,然后研究了其对CRC细胞在体外对5-FU的潜在敏感性。还研究了对PI3K / AKT途径的潜在影响。除了G1细胞周期阻滞外,还检测到5-FU和VER之间的协同细胞毒性相互作用。还观察到主要通过影响Bax和Bcl-2而在较小程度上降低了Bcl-xL和p53,从而增强了细胞凋亡。此外,与VER结合的5-FU能够显着降低PI3K和p-AKT /总AKT比率。总体而言,这些结果表明,VER作为佐剂治疗可能通过靶向PI3K / AKT途径降低CRC细胞对5-FU的耐药性而发挥潜在的作用。

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