非洲爪蟾唾液腺FS48通过阻断电压门控K+通道对NCI-H460细胞的体外抗癌作用

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2023-03-01 DOI:10.2478/acph-2023-0010
Weichen Xiong, Huizhen Fan, Qingye Zeng, Zhenhui Deng, Guanhui Li, Wancheng Lu, Bei Zhang, Shian Lai, Xin Chen, Xueqing Xu
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引用次数: 1

摘要

电压门控K+ (Kv)通道在包括肺癌细胞在内的多种癌细胞的细胞过程中发挥作用。我们之前从非洲爪蚤中鉴定并报道了一种唾液蛋白FS48,该蛋白在HEK 293T细胞中表现出对Kv1.1-1.3通道的抑制活性。然而,FS48是否对表达Kv通道的癌细胞有抑制作用尚不清楚。本研究旨在通过膜片钳、MTT、伤口愈合、transwell、明胶酶酶谱、qRT-PCR和WB检测揭示FS48对Kv通道和NCI-H460人肺癌细胞的影响。结果表明,FS48能有效抑制NCI-H460细胞的Kv电流、迁移和侵袭,且呈剂量依赖性,但不能抑制细胞增殖。Kv1.1和Kv1.3 mRNA和蛋白的表达显著降低。最后,FS48降低了MMP-9的mRNA水平,同时提高了TIMP-1的mRNA水平。本研究首次强调了吸血节肢动物唾液源蛋白可以通过Kv通道抑制肿瘤细胞的生理活动。此外,FS48可以作为一种打击表达Kv通道的肿瘤细胞的化合物。
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The in vitro anticancer effects of FS48 from salivary glands of Xenopsylla cheopis on NCI-H460 cells via its blockage of voltage-gated K+ channels.

Voltage-gated K+ (Kv) channels play a role in the cellular processes of various cancer cells, including lung cancer cells. We previously identified and reported a salivary protein from the Xenopsylla cheopis, FS48, which exhibited inhibitory activity against Kv1.1-1.3 channels when assayed in HEK 293T cells. However, whether FS48 has an inhibitory effect on cancer cells expressing Kv channels is unclear. The present study aims to reveal the effects of FS48 on the Kv channels and the NCI-H460 human lung cancer cells through patch clamp, MTT, wound healing, transwell, gelatinase zymography, qRT-PCR and WB assays. The results demonstrated that FS48 can be effective in suppressing the Kv currents, migration, and invasion of NCI-H460 cells in a dose-dependent manner, despite the failure to inhibit the proliferation. Moreover, the expression of Kv1.1 and Kv1.3 mRNA and protein were found to be significantly reduced. Finally, FS48 decreases the mRNA level of MMP-9 while increasing TIMP-1 mRNA level. The present study highlights for the first time that blood-sucking arthropod saliva-derived protein can inhibit the physiological activities of tumour cells via the Kv channels. Furthermore, FS48 can be taken as a hit compound against the tumour cells expressing Kv channels.

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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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