Suppr超能文献

来自日本杏(“梅”)的新型抗增殖剂MK615在体外诱导结肠癌细胞发生显著自噬。

New anti-proliferative agent, MK615, from Japanese apricot "Prunus mume" induces striking autophagy in colon cancer cells in vitro.

作者信息

Mori Shozo, Sawada Tokihiko, Okada Toshie, Ohsawa Tatsushi, Adachi Masakazu, Keiichi Kubota

机构信息

Second Department of Surgery, Dokkyo University School of Medicine, Kitakobayashi 880, Mibu, Shimotsuga, Tochigi 321-0293, Japan.

出版信息

World J Gastroenterol. 2007 Dec 28;13(48):6512-7. doi: 10.3748/wjg.v13.i48.6512.

Abstract

AIM

To investigate the anti-neoplastic effects of MK615, an extract from the Japanese apricot (Prunus mume), against colon cancer cells.

METHODS

Three colon cancer cell lines, SW480, COLO, and WiDr, were cultured with MK615. Growth inhibition was evaluated by cell proliferation assay and killing activity was determined by lactate dehydrogenase assay. Induction of apoptosis was evaluated by annexin V flow cytometry. Morphological changes were studied by light and electron microscopy, and immunofluorescence staining with Atg8.

RESULTS

MK615 inhibited growth and lysed SW480, COLO and WiDr cells in a dose-dependent manner. Annexin V flow cytometry showed that MK615 induced apoptosis after 6 h incubation, at which point the occurrence of apoptotic cells was 68.0%, 65.7% and 64.7% for SW480, COLO, and WiDr cells, respectively. Light and electron microscopy, and immunofluorescence staining with Atg8 revealed that MK615 induced massive cytoplasmic vacuoles (autophagosomes) in all three cell lines.

CONCLUSION

MK615 has an anti-neoplastic effect against colon cancer cells. The effect may be exerted by induction of apoptosis and autophagy.

摘要

目的

研究青梅提取物MK615对结肠癌细胞的抗肿瘤作用。

方法

用MK615培养三种结肠癌细胞系SW480、COLO和WiDr。通过细胞增殖试验评估生长抑制情况,通过乳酸脱氢酶试验测定杀伤活性。用膜联蛋白V流式细胞术评估细胞凋亡的诱导情况。通过光学显微镜和电子显微镜研究形态学变化,并用Atg8进行免疫荧光染色。

结果

MK615以剂量依赖的方式抑制SW480、COLO和WiDr细胞的生长并使其裂解。膜联蛋白V流式细胞术显示,孵育6小时后MK615诱导细胞凋亡,此时SW480、COLO和WiDr细胞的凋亡细胞发生率分别为68.0%、65.7%和64.7%。光学显微镜和电子显微镜以及用Atg8进行的免疫荧光染色显示,MK615在所有三种细胞系中均诱导大量细胞质空泡(自噬体)形成。

结论

MK615对结肠癌细胞具有抗肿瘤作用。这种作用可能是通过诱导细胞凋亡和自噬来实现的。

相似文献

4
MK615 inhibits pancreatic cancer cell growth by dual inhibition of Aurora A and B kinases.
World J Gastroenterol. 2008 Mar 7;14(9):1378-82. doi: 10.3748/wjg.14.1378.
5
6
Anticancer properties of Prunus mume extracts (Chinese plum, Japanese apricot).
J Ethnopharmacol. 2020 Jan 10;246:112215. doi: 10.1016/j.jep.2019.112215. Epub 2019 Sep 3.
8
L-securinine induced the human colon cancer SW480 cell autophagy and its molecular mechanism.
Fitoterapia. 2011 Dec;82(8):1258-64. doi: 10.1016/j.fitote.2011.08.015. Epub 2011 Sep 1.
9
MK615: a new therapeutic approach for the treatment of oral disease.
Med Hypotheses. 2011 Aug;77(2):258-60. doi: 10.1016/j.mehy.2011.04.027. Epub 2011 May 11.

引用本文的文献

2
Therapeutic Potential of Species in Gastrointestinal Oncology.
Cancers (Basel). 2025 Mar 10;17(6):938. doi: 10.3390/cancers17060938.
6
Comprehensive Review of Phytochemical Constituents, Pharmacological Properties, and Clinical Applications of .
Front Pharmacol. 2021 May 28;12:679378. doi: 10.3389/fphar.2021.679378. eCollection 2021.
7
Medicinal Plants in the Prevention and Treatment of Colon Cancer.
Oxid Med Cell Longev. 2019 Dec 4;2019:2075614. doi: 10.1155/2019/2075614. eCollection 2019.
8
In Vivo Antitumor Effects of MK615 Led by PD-L1 Downregulation.
Integr Cancer Ther. 2018 Sep;17(3):646-653. doi: 10.1177/1534735418766403. Epub 2018 Apr 18.
9
Effects of Siebold & Zucc. in the pacemaking activity of interstitial cells of Cajal in murine small intestine.
Exp Ther Med. 2017 Jan;13(1):327-334. doi: 10.3892/etm.2016.3963. Epub 2016 Dec 7.
10
Dietary interactions with the bacterial sensing machinery in the intestine: the plant polyphenol case.
Front Genet. 2014 Apr 4;5:64. doi: 10.3389/fgene.2014.00064. eCollection 2014.

本文引用的文献

1
The inhibitors of apoptosis (IAPs) as cancer targets.
Apoptosis. 2007 Sep;12(9):1543-68. doi: 10.1007/s10495-007-0087-3.
3
Autophagy as a mechanism of radiation sensitization in breast tumor cells.
Autophagy. 2007 May-Jun;3(3):249-50. doi: 10.4161/auto.3723. Epub 2007 May 19.
4
Therapeutic targeting of apoptotic pathways in cancer.
Curr Drug Targets. 2006 Oct;7(10):1361-9. doi: 10.2174/138945006778559175.
5
Autophagy for cancer therapy through inhibition of pro-apoptotic proteins and mammalian target of rapamycin signaling.
J Biol Chem. 2006 Dec 1;281(48):36883-90. doi: 10.1074/jbc.M607094200. Epub 2006 Sep 27.
6
Surgical adjuvant therapy for colorectal cancer: current approaches and future directions.
Ann Surg Oncol. 2006 Aug;13(8):1021-34. doi: 10.1245/ASO.2006.08.015. Epub 2006 Jul 29.
7
Lysosomal turnover, but not a cellular level, of endogenous LC3 is a marker for autophagy.
Autophagy. 2005 Jul;1(2):84-91. doi: 10.4161/auto.1.2.1697. Epub 2005 Jul 31.
9
First- and second-line therapy of metastatic colorectal cancer.
Expert Rev Anticancer Ther. 2006 Jun;6(6):921-30. doi: 10.1586/14737140.6.6.921.
10
Autophagy: molecular machinery for self-eating.
Cell Death Differ. 2005 Nov;12 Suppl 2(Suppl 2):1542-52. doi: 10.1038/sj.cdd.4401765.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验