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表面活性素通过在黑色素瘤皮肤癌中引发过敏反应发挥抗癌作用。

Surfactin exerts an anti-cancer effect through inducing allergic reactions in melanoma skin cancer.

作者信息

Kim Hee-Yun, Jung Hanchul, Kim Hyung-Min, Jeong Hyun-Ja

机构信息

Biochip Research Center, Hoseo University, Asan, Chungnam 31499, Republic of Korea.

Department of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.

出版信息

Int Immunopharmacol. 2021 Oct;99:107934. doi: 10.1016/j.intimp.2021.107934. Epub 2021 Jul 4.

Abstract

Surfactin is a mast cell degranulator, that increases the immune response via the degranulation of mast cells. Recently, numerous studies reported that allergic reactions play an important role in the reduction of melanoma development. So, this study aimed to investigate the anti-cancer effects of surfactin in a melanoma skin cancer in vivo model and a melanoma cell line, B16F10. Oral administration of surfactin significantly increased survival rate and reduced tumor growth and tumor weight on melanoma skin cancer in vivo model. Surfactin significantly increased infiltration of mast cells and levels of histamine. Surfactin significantly enhanced levels of IgE and immune-enhancing mediators, such as interferon-γ, interleukin (IL)-2, IL-6, IL-12, and tumor necrosis factor-α in serum and melanoma tissues. Activities of caspase-3, 8, and 9 were significantly enhanced by oral administration of surfactin. In vitro model, surfactin significantly increased B16F10 cell death via activation of caspase-3, 8, and 9 in a dose-dependent manner. Overall, our results indicate that surfactin has a significant anti-cancer effect on melanoma skin cancer through indirectly or directly inducing apoptosis of B16F10 melanoma cells. Also, these findings suggest that it will contribute to a novel perception into the role of allergic reactions in melanoma.

摘要

表面活性素是一种肥大细胞脱颗粒剂,可通过肥大细胞脱颗粒增强免疫反应。最近,大量研究报道过敏反应在黑色素瘤发展的抑制中起重要作用。因此,本研究旨在探讨表面活性素在黑色素瘤皮肤癌体内模型和黑色素瘤细胞系B16F10中的抗癌作用。在黑色素瘤皮肤癌体内模型中,口服表面活性素显著提高了生存率,降低了肿瘤生长和肿瘤重量。表面活性素显著增加了肥大细胞的浸润和组胺水平。表面活性素显著提高了血清和黑色素瘤组织中IgE以及免疫增强介质如干扰素-γ、白细胞介素(IL)-2、IL-6、IL-12和肿瘤坏死因子-α的水平。口服表面活性素显著增强了半胱天冬酶-3、8和9的活性。在体外模型中,表面活性素通过以剂量依赖的方式激活半胱天冬酶-3、8和9,显著增加了B16F10细胞死亡。总体而言,我们的结果表明,表面活性素通过间接或直接诱导B16F10黑色素瘤细胞凋亡,对黑色素瘤皮肤癌具有显著的抗癌作用。此外,这些发现表明,它将有助于对过敏反应在黑色素瘤中的作用产生新的认识。

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