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小叶裂榄(Bursera microphylla A Gray)的己烷馏分在人源癌细胞系中诱导p21介导的抗增殖和促凋亡作用。

The Hexane Fraction of Bursera microphylla A Gray Induces p21-Mediated Antiproliferative and Proapoptotic Effects in Human Cancer-Derived Cell Lines.

作者信息

Adorisio Sabrina, Fierabracci Alessandra, Gigliarelli Giulia, Muscari Isabella, Cannarile Lorenza, Liberati Anna Marina, Marcotullio Maria Carla, Riccardi Carlo, Curini Massimo, Robles Zepeda Ramon Enrique, Delfino Domenico V

机构信息

1 Section of Pharmacology, Department of Medicine, University of Perugia, Italy.

2 Infectivology and Clinical Trials Area, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.

出版信息

Integr Cancer Ther. 2017 Sep;16(3):426-435. doi: 10.1177/1534735416688413. Epub 2017 Jan 23.

DOI:10.1177/1534735416688413
PMID:28110563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5759934/
Abstract

Bursera microphylla (BM), one of the common elephant trees, is widely distributed in the Sonoran desert in Mexico. The Seri ethnic group in the Sonoran desert uses BM as an anti-inflammatory and painkiller drug for the treatment of sore throat, herpes labialis, abscessed tooth, and wound healing. Dried stems and leaves of BM are used in a tea to relieve painful urination and to stimulate bronchial secretion. Furthermore, BM is used for fighting venereal diseases. To investigate the effects of the hexane fraction of resin methanol extract (BM-H) on cell growth, the acute myeloid cell line (OCI-AML3) was treated with 250, 25, or 2.5 µg/mL of BM-H. The first 2 concentrations were able to significantly decrease OCI-AML3 cell number. This reduced cell number was associated with decreased S-phase, blockade of G/M phase of the cell cycle, and increased cell death. Similar results were obtained on all tested tumor cell lines of different origins. We found that blockade of the cell cycle was a result of upregulation of p21 protein in a p53-independent way. Increase of p21 was possibly a result of upstream upregulation of p-ERK (which stabilizes p21 protein) and downregulation of p-38 (which promotes its degradation). Regarding cell death, activation of caspase-3, but not of caspase-8 or -9, was detectable after BM-H treatment. In conclusion, these data suggest that BM-H inhibited proliferation of cell lines mainly by a p21-dependent, p53-independent mechanism and promoted apoptosis through activation of caspase-3 but not caspase-8 or -9.

摘要

小叶裂榄(BM)是常见的象树之一,广泛分布于墨西哥的索诺兰沙漠。索诺兰沙漠的塞里族将BM用作消炎止痛药,用于治疗喉咙痛、唇疱疹、脓肿牙和伤口愈合。BM的干燥茎和叶被用于泡茶,以缓解尿痛并刺激支气管分泌。此外,BM还用于治疗性病。为了研究树脂甲醇提取物的己烷馏分(BM-H)对细胞生长的影响,用250、25或2.5μg/mL的BM-H处理急性髓性细胞系(OCI-AML3)。前两个浓度能够显著减少OCI-AML3细胞数量。这种细胞数量的减少与S期减少、细胞周期G/M期阻滞以及细胞死亡增加有关。在所有测试的不同来源的肿瘤细胞系上都得到了类似的结果。我们发现细胞周期阻滞是p21蛋白以p53非依赖方式上调的结果。p21的增加可能是p-ERK上游上调(使p21蛋白稳定)和p-38下调(促进其降解)的结果。关于细胞死亡,BM-H处理后可检测到caspase-3的激活,但未检测到caspase-8或-9的激活。总之,这些数据表明,BM-H主要通过p21依赖、p53非依赖机制抑制细胞系增殖,并通过激活caspase-3而非caspase-8或-9促进细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/0956d25f7c6d/10.1177_1534735416688413-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/ea5a4be8e0f7/10.1177_1534735416688413-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/5ab8f8fc839d/10.1177_1534735416688413-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/4f5a41c12b3a/10.1177_1534735416688413-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/547920a0e41f/10.1177_1534735416688413-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/4e083479f75c/10.1177_1534735416688413-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/1f9c164628f4/10.1177_1534735416688413-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/81e6616e40e9/10.1177_1534735416688413-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/f06e5a062e66/10.1177_1534735416688413-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/5f43c8273be5/10.1177_1534735416688413-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/f49eb629acdf/10.1177_1534735416688413-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/0956d25f7c6d/10.1177_1534735416688413-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/ea5a4be8e0f7/10.1177_1534735416688413-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/5ab8f8fc839d/10.1177_1534735416688413-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/4f5a41c12b3a/10.1177_1534735416688413-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/547920a0e41f/10.1177_1534735416688413-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/4e083479f75c/10.1177_1534735416688413-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/1f9c164628f4/10.1177_1534735416688413-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/81e6616e40e9/10.1177_1534735416688413-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/f06e5a062e66/10.1177_1534735416688413-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/5f43c8273be5/10.1177_1534735416688413-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/f49eb629acdf/10.1177_1534735416688413-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3453/5759934/0956d25f7c6d/10.1177_1534735416688413-fig11.jpg

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