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青梅多酚通过 PI3K/AKT/FOXO1 通路诱导人肺癌 A549 细胞凋亡的机制新见解。

New Insights into the Mechanisms of Polyphenol from Plum Fruit Inducing Apoptosis in Human Lung Cancer A549 Cells Via PI3K/AKT/FOXO1 Pathway.

机构信息

School of Life Science and Biotechnology, Yangtze Normal University, 16 Juxian Road, Fuling district, Chongqing, 408100, China.

School of Aerospace Medicine, Fourth Military Medical University, No. 169, Changle-West road, Xi'an, 710032, Shaanxi, China.

出版信息

Plant Foods Hum Nutr. 2021 Mar;76(1):125-132. doi: 10.1007/s11130-021-00882-y. Epub 2021 Feb 27.

Abstract

Recent studies have been found that polyphenols from plums fruits can inhibit the proliferation of multiple cancer cells, while the molecular mechanism was unclear. This study aimed to investigate the molecular mechanism underlying the pro-apoptotic effect of purified plum polyphenols (PPP) on human lung cancer A549 cells. Quercitrin (quercetin-3-O-glucoside, 814.19 ± 40.71 mg/g) was identified as the primary polyphenol in PPP via ultra high-performance liquid chromatography coupled with triple quadrupole mass spectrometry (UHPLC-QqQ-MS/MS). PPP showed a strong capacity for inhibiting the proliferation of the A549 cells by inducing apoptosis, which was reflected by an increase in the Bax/Bcl-2 ratio. Additionally, the inhibitory rate of PPP on the A549 cells were higher than that of vitamin C when the treatment dose exceeded 160 μg/mL. Transcriptome analysis suggested that PPP-induced apoptosis was closely associated with regulating the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT)/forkhead box protein O 1 (FOXO1) pathway in the A549 cells. Subsequently, as an activator of AKT, SC79 was applied to confirm that the inhibition of AKT phosphorylation play an important role in the PPP-induced apoptosis of the A549 cells. These results illustrated the potential of PPP as a dietary compound for the prevention of cancer or for use during chemotherapy.

摘要

最近的研究发现,李属果实中的多酚可以抑制多种癌细胞的增殖,但其分子机制尚不清楚。本研究旨在探讨纯化李属多酚(PPP)对人肺癌 A549 细胞促凋亡作用的分子机制。通过超高效液相色谱-串联三重四极杆质谱联用技术(UHPLC-QqQ-MS/MS)鉴定 PPP 中的主要多酚为槲皮素-3-O-葡萄糖苷(quercitrin,814.19±40.71 mg/g)。PPP 通过诱导细胞凋亡强烈抑制 A549 细胞的增殖,这反映在 Bax/Bcl-2 比值的增加上。此外,当处理剂量超过 160 μg/mL 时,PPP 对 A549 细胞的抑制率高于维生素 C。转录组分析表明,PPP 诱导的细胞凋亡与调节 A549 细胞中的磷脂酰肌醇 3-激酶(PI3K)/蛋白激酶 B(AKT)/叉头框蛋白 O1(FOXO1)途径密切相关。随后,作为 AKT 的激活剂,SC79 被用于证实 AKT 磷酸化的抑制在 PPP 诱导的 A549 细胞凋亡中起着重要作用。这些结果表明 PPP 作为一种预防癌症或化疗期间使用的膳食化合物具有潜力。

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