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红曲米糠提取物中原花青素丰富部分诱导 HepG2 肝癌细胞凋亡。

The Proanthocyanidin-Rich Fraction Obtained from Red Rice Germ and Bran Extract Induces HepG2 Hepatocellular Carcinoma Cell Apoptosis.

机构信息

Anticarcinogenesis and Apoptosis Research Cluster, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Molecules. 2019 Feb 23;24(4):813. doi: 10.3390/molecules24040813.

Abstract

This study aims to determine the anti-carcinogenic effects of the proanthocyanidin-rich fraction (PRFR) obtained from red rice germ and bran extract on HepG2 cells. The PRFR obtained from red rice germ and bran extract could reduce the cell viability of HepG2 cells as shown by the IC value at 20 µg/mL. Notably, PRFR concentrations at 20 and 40 µg/mL significantly increased the number of cells in the G2/M phase from 25.7% ± 1.4%in the control group to 36.2% ± 3.4% ( < 0.01) and 48.9% ± 2.6% ( < 0.0001), respectively, suggesting that the cells were arrested in this phase, which was confirmed by the reduction of survival proteins, including cyclin B1 and cdc25. Moreover, the PRFR at 20 and 40 µg/mL could induce cell death via the apoptosis cascade, indicated by the percentage of total apoptotic cells from 9.9% ± 3.1% in the control group to 41.1 ± 3.9 ( < 0.0001) and 82.2% ± 5.8% ( < 0.0001), respectively. This was clarified by increasing apoptotic proteins (such as cleaved PARP-1, cleaved caspase-8 and cleaved caspase-3) and decreasing anti-apoptotic protein survivin without p53 alterations. These results demonstrated that the PRFR obtained from red rice germ and bran extract could inhibit cell proliferation and induce cell apoptosis in HepG2 cells via survivin, which could potentially serve as a new target for cancer therapeutics making it an excellent "lead candidate" molecule for in vivo proof-of concept studies.

摘要

本研究旨在确定从红米胚芽和糠提取的原花青素丰富部分(PRFR)对 HepG2 细胞的抗癌作用。从红米胚芽和糠提取的 PRFR 可降低 HepG2 细胞的细胞活力,IC 值在 20μg/ml 时可见。值得注意的是,PRFR 在 20 和 40μg/ml 浓度下,可使对照组中处于 G2/M 期的细胞数量从 25.7%±1.4%显著增加至 36.2%±3.4%(<0.01)和 48.9%±2.6%(<0.0001),表明细胞在此期被阻滞,这一点通过存活蛋白(包括细胞周期蛋白 B1 和 cdc25)的减少得到证实。此外,PRFR 在 20 和 40μg/ml 浓度下可通过凋亡级联诱导细胞死亡,总凋亡细胞的百分比从对照组的 9.9%±3.1%分别增加到 41.1%±3.9%(<0.0001)和 82.2%±5.8%(<0.0001)。这一点通过增加凋亡蛋白(如裂解的 PARP-1、裂解的 caspase-8 和裂解的 caspase-3)和减少抗凋亡蛋白 survivin 而没有 p53 改变来阐明。这些结果表明,从红米胚芽和糠提取的 PRFR 可通过 survivin 抑制 HepG2 细胞的增殖并诱导细胞凋亡,这可能成为癌症治疗的新靶点,使其成为体内概念验证研究的优秀“先导候选”分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e5/6412498/82de5174e66b/molecules-24-00813-g001.jpg

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