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Therapeutic Use of MicroRNAs in Cancer.微小RNA在癌症治疗中的应用
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Identification of a hypoxia-regulated miRNA signature in bladder cancer and a role for miR-145 in hypoxia-dependent apoptosis.膀胱癌中缺氧调节的miRNA特征的鉴定及miR-145在缺氧依赖性凋亡中的作用
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Epigenetically altered miR-193b targets cyclin D1 in prostate cancer.在前列腺癌中,表观遗传改变的miR-193b靶向细胞周期蛋白D1 。
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Primary laryngeal cancer-derived miR-193b induces interleukin-10-expression monocytes.原发性喉癌来源的 miR-193b 诱导白细胞介素 10 表达的单核细胞。
Cancer Invest. 2015 Mar;33(2):29-33. doi: 10.3109/07357907.2014.988344. Epub 2014 Dec 17.
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Tanshinone IIA inhibits gastric carcinoma AGS cells through increasing p-p38, p-JNK and p53 but reducing p-ERK, CDC2 and cyclin B1 expression.丹参酮 IIA 通过增加 p-p38、p-JNK 和 p53,同时减少 p-ERK、CDC2 和细胞周期蛋白 B1 的表达来抑制胃癌 AGS 细胞。
Anticancer Res. 2014 Dec;34(12):7097-110.
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Tanshinone IIA inhibits viral oncogene expression leading to apoptosis and inhibition of cervical cancer.丹参酮 IIA 通过抑制病毒癌基因表达诱导宫颈癌凋亡。
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10
NLRP3 gene is associated with ulcerative colitis (UC), but not Crohn's disease (CD), in Chinese Han population.在中国汉族人群中,NLRP3基因与溃疡性结肠炎(UC)相关,但与克罗恩病(CD)无关。
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丹参酮IIA通过p53-细胞周期蛋白B1/细胞分裂周期蛋白2抑制人鼻咽癌细胞的增殖并诱导其凋亡。

Tanshinone IIA inhibits proliferation and induces apoptosis of human nasopharyngeal carcinoma cells via p53-cyclin B1/CDC2.

作者信息

Liu Bin, Liu Lixia, Zang Aimin, Song Zizheng, Yang Hua, Wang Zhiyu, Shang Yanhong, Ma Tao, Zhang Yonggang

机构信息

Department of Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.

Department of Functions Branch, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.

出版信息

Oncol Lett. 2019 Sep;18(3):3317-3322. doi: 10.3892/ol.2019.10658. Epub 2019 Jul 24.

DOI:10.3892/ol.2019.10658
PMID:31452810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6704284/
Abstract

Tanshinone IIA exhibits natural antioxidative and antineoplastic activity. However, to the best of our knowledge, the effects of tanshinone IIA on human nasopharyngeal carcinoma cells remains unknown. The present study aimed to investigate whether tanshinone IIA inhibits proliferation and induces apoptosis of human nasopharyngeal carcinoma cells via p53-cyclin B1/cell division cycle gene 2 (CDC2). Cell proliferation, cytotoxicity and apoptosis of 13-9B cells were evaluated by an MTT assay, lactate dehydrogenase assay and flow cytometry, respectively. ELISA and western blot analysis were used to analyze caspase-3 activity and poly (ADP-ribose) polymerase (PARP), p53, cyclin B1 and CDC2 protein expression in 13-9B cells. Treatment of 13-9B cells with tanshinone IIA significantly suppressed cell proliferation and significantly induced cytotoxicity and apoptosis of 13-9B cells. Furthermore, tanshinone IIA significantly increased caspase-3 activity, and significantly increased the protein expression levels of PARP, p53, cyclin B1 and CDC2 in 13-9B cells. In summary, the current results indicate that tanshinone IIA inhibits proliferation and induces apoptosis of human nasopharyngeal carcinoma cells via PARP, p53, cyclin B1/CDC2 and caspase-3-mediated signaling.

摘要

丹参酮IIA具有天然的抗氧化和抗肿瘤活性。然而,据我们所知,丹参酮IIA对人鼻咽癌细胞的作用仍不清楚。本研究旨在探讨丹参酮IIA是否通过p53-细胞周期蛋白B1/细胞分裂周期基因2(CDC2)抑制人鼻咽癌细胞的增殖并诱导其凋亡。分别采用MTT法、乳酸脱氢酶法和流式细胞术评估13-9B细胞的细胞增殖、细胞毒性和凋亡情况。采用ELISA和蛋白质印迹分析来分析13-9B细胞中半胱天冬酶-3活性以及聚(ADP-核糖)聚合酶(PARP)、p53、细胞周期蛋白B1和CDC2的蛋白表达。用丹参酮IIA处理13-9B细胞可显著抑制细胞增殖,并显著诱导13-9B细胞的细胞毒性和凋亡。此外,丹参酮IIA可显著提高13-9B细胞中半胱天冬酶-3活性,并显著提高PARP、p53、细胞周期蛋白B1和CDC2的蛋白表达水平。总之,目前结果表明丹参酮IIA通过PARP、p53、细胞周期蛋白B1/CDC2和半胱天冬酶-3介导的信号通路抑制人鼻咽癌细胞的增殖并诱导其凋亡。