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Hydrolysis product of Nigella A obtained from Nigella glandulifera Freyn seeds promotes apoptosis and AMPK-mediated autophagy in human colon cancer SW620 cells

机译:从黑执果念珠菌种子获得的黑执事A的水解产物促进人结肠癌SW620细胞的凋亡和AMPK介导的自噬

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Paper description:Nigella B (NB) is the hydrolysis product of Nigella A (NA) which is extracted from the seeds of Nigella glandulifera Freyn and has been reported to possess several beneficial characteristics, including an anticancer effect.This work demonstrates for the first time the anticancer effect of NA and the mechanism of NB on inducing autophagy in combination with the apoptotic pathway, in human colon cancer cell lines.Our study reveals an anticancer function for NA and NB in colon cancer and supports the use of NA as an antitumor pro-drug and NB as a novel therapeutic drug.: Nigella B (NB) is the hydrolysis product of Nigella A (NA), which is extracted from the seeds of Nigella glandulifera Freyn. NB has several beneficial characteristics, including antiproliferative activity against several cancer cell lines. In this study, we analyzed the in vitro and in vivo anticancer activity of both NA and NB as well as the potential molecular mechanisms behind the actions of NB. We found that NB treatment led to autophagy and soft apoptosis in colon cancer cells (SW620). NA treatment had no effect on either. Further study showed that NB treatment in SW620 cells led to inhibited phosphorylated mammalian target of rapamycin (p-mTOR) expression but increased phosphorylated-5' adenosine monophosphate protein kinase (AMPK) expression, a key regulator of autophagy. This suggests that the AMPK-mTOR pathway plays a crucial role in autophagy induction. Separate in vivo studies using NA (40 mg/kg, intragastric administration (i.g.)) and NB (40 mg/kg, i.g.) resulted in inhibited tumor growth in nude mice by 42.82% and 37.20% respectively, when compared with vehicle-administered animals. In vitro tumor protein expression was consistent with its expression in vitro . Taken together, our results reveal an anticancer function for NA and NB in colon cancer and support the use of NA as an antitumor prodrug, and NB as a novel therapeutic drug.
机译:论文描述:黑藻B(NB)是黑藻A(NA)的水解产物,该产物是从黑乳李(Nigella glandulifera Freyn)种子中提取的,据报道具有多种有益特性,包括抗癌作用。 NA和NB诱导凋亡的机制与细胞凋亡途径相结合,在人结肠癌细胞系中的表达。我们的研究揭示了NA和NB在结肠癌中的抗癌作用,并支持将NA用作抗肿瘤药-药物和NB作为一种新型治疗药物。Nigella B(NB)是Nigella A(NA)的水解产物,是从Nigella glandulifera Freyn的种子中提取的。 NB具有几个有益的特性,包括对几种癌细胞系的抗增殖活性。在这项研究中,我们分析了NA和NB的体外和体内抗癌活性,以及​​NB作用背后的潜在分子机制。我们发现,NB处理导致结肠癌细胞(SW620)自噬和软凋亡。 NA治疗对两者均无影响。进一步的研究表明,在SW620细胞中进行NB处理可抑制哺乳动物雷帕霉素靶标(p-mTOR)的表达,但会增加磷酸化5'腺苷单磷酸蛋白激酶(AMPK)的表达,这是自噬的关键调节因子。这表明AMPK-mTOR途径在自噬诱导中起关键作用。与溶媒给药相比,使用NA(40 mg / kg,胃内给药(ig))和NB(40 mg / kg,ig)进行的单独体内研究分别导致裸鼠体内肿瘤生长抑制42.82%和37.20%动物。体外肿瘤蛋白表达与体外表达一致。综上所述,我们的结果揭示了NA和NB在结肠癌中的抗癌功能,并支持将NA用作抗肿瘤前药,并将NB用作新型治疗药物。

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