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蜂毒肽通过抑制乳腺癌细胞中的PI3K/Akt/mTOR信号通路来抑制表皮生长因子诱导的细胞迁移和侵袭。

Melittin suppresses EGF-induced cell motility and invasion by inhibiting PI3K/Akt/mTOR signaling pathway in breast cancer cells.

作者信息

Jeong Yun-Jeong, Choi Yongsoo, Shin Jae-Moon, Cho Hyun-Ji, Kang Jeong-Han, Park Kwan-Kyu, Choe Jung-Yoon, Bae Young-Seuk, Han Sang-Mi, Kim Cheorl-Ho, Chang Hyeun-Wook, Chang Young-Chae

机构信息

Research Institute of Biomedical Engineering and Department of Medicine, Catholic University of Daegu School of Medicine, Daegu 705-718, Republic of Korea.

National Medicine Center, Korea Institute of Science and Technology, Gangneung 210-340, Republic of Korea.

出版信息

Food Chem Toxicol. 2014 Jun;68:218-25. doi: 10.1016/j.fct.2014.03.022. Epub 2014 Mar 25.

Abstract

Bee venom is a natural compound produced by the honey bee (Apis mellifera), and has been reported as having the biological and pharmacological activities, including anti-bacterial, anti-viral and anti-inflammation. In the present study, the inhibitory effects of bee venom and its major peptide components on the tumor invasion were demonstrated. It was confirmed the inhibitory effects of bee venom, melittin, and apamin on the EGF-induced invasion of breast cancer cells. Transwell invasion and wound-healing assays showed that bee venom and melittin significantly inhibits the EGF-induced invasion and migration of breast cancer cells. Also, bee venom and melittin reduced the EGF-stimulated F-actin reorganization at the leading edge, but apamin did not affect. Particularly, melittin inhibited the EGF-induced MMP-9 expression via blocking the NF-κB and PI3K/Akt/mTOR pathway. In addition, melittin significantly suppressed the EGF-induced FAK phosphorylation through inhibition of mTOR/p70S6K/4E-BP1 pathway. These results suggest that inhibitory effects of melittin on breast cancer cell motility and migration may be related to the inhibition of mTOR pathway.

摘要

蜂毒是蜜蜂(西方蜜蜂)产生的一种天然化合物,据报道具有生物和药理活性,包括抗菌、抗病毒和抗炎作用。在本研究中,证明了蜂毒及其主要肽成分对肿瘤侵袭的抑制作用。证实了蜂毒、蜂毒肽和蜂毒明肽对表皮生长因子(EGF)诱导的乳腺癌细胞侵袭具有抑制作用。Transwell侵袭实验和伤口愈合实验表明,蜂毒和蜂毒肽显著抑制EGF诱导的乳腺癌细胞侵袭和迁移。此外,蜂毒和蜂毒肽减少了前缘处EGF刺激的F-肌动蛋白重组,但蜂毒明肽没有影响。特别地,蜂毒肽通过阻断核因子κB(NF-κB)和磷脂酰肌醇-3激酶/蛋白激酶B/哺乳动物雷帕霉素靶蛋白(PI3K/Akt/mTOR)途径抑制EGF诱导的基质金属蛋白酶-9(MMP-9)表达。此外,蜂毒肽通过抑制mTOR/p70核糖体蛋白S6激酶/真核细胞起始因子4E结合蛋白1(mTOR/p70S6K/4E-BP1)途径显著抑制EGF诱导的黏着斑激酶(FAK)磷酸化。这些结果表明,蜂毒肽对乳腺癌细胞运动性和迁移的抑制作用可能与mTOR途径的抑制有关。

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