Suppr超能文献

零聚体衍生肽9R、9S1R和124R对NCI-60细胞株和正常细胞系的影响。

The effect of Nullomer-derived peptides 9R, 9S1R and 124R on the NCI-60 panel and normal cell lines.

作者信息

Alileche Abdelkrim, Hampikian Greg

机构信息

Biology Department Room SN-215, Boise State University, 1910 University Drive, Boise, ID, 83725, USA.

出版信息

BMC Cancer. 2017 Aug 9;17(1):533. doi: 10.1186/s12885-017-3514-z.

Abstract

BACKGROUND

Nullomer peptides are the smallest sequences absent from databases of natural proteins. We first began compiling a list of absent 5-amino acid strings in 2006 (1). We report here the effects of Nullomer-derived peptides 9R, 9S1R and 124R on the NCI-60 panel, derived from human cancers of 9 organs (kidney, ovary, skin melanoma, lung, brain, lung, colon, prostate and the hematopoietic system), and four normal cell lines (endothelial HUVEC, skin fibroblasts BJ, colon epithelial FHC and normal prostate RWPE-1).

METHODS

NCI-60 cancer cell panel and four normal cell lines were cultured in vitro in RPMI1640 supplemented with 10% Hyclone fetal bovine serum and exposed for 48 h to 5 μM, 25 μM and 50 μM of peptides 9R, 9S1R and 124R. Viability was assessed by CCK-8 assay. For peptide ATP depletion effects, one cell line representing each organ in the NCI-60 panel, and four normal cell lines were exposed to 50 μM of peptides 9R, 9S1R and 124R for 3 h. The ATP content was assessed in whole cells, and their supernatants.

RESULTS

Peptides 9S1R and 9R are respectively lethal to 95 and 81.6% of the 60 cancer cell lines tested. Control peptide 124R has no effect on the growth of these cells. Especially interesting the fact that peptides 9R and 9S1R are capable of killing drug-resistant and hormone-resistant cell lines, and even cancer stem cells. Peptides 9R and 9S1R have a broader activity spectrum than many cancer drugs in current use, can completely deplete cellular ATP within 3 h, and are less toxic to 3 of the 4 normal cell lines tested than they are to several cancers.

CONCLUSIONS

Nullomer peptides 9R and 9S1R have a large broad lethal effect on cancer cell lines derived from nine organs represented in the NCI-60 panel. This broad activity crosses many of the categorical divisions used in the general classification of cancers: solid vs liquid cancers, drug sensitive vs drug resistant, hormone sensitive vs hormone resistant, cytokine sensitive vs cytokine non sensitive, slow growing vs rapid growing, differentiated vs dedifferentiated cancers. Furthermore peptides 9R and 9S1R are lethal to cancer stem cells and breast canrcinosarcoma.

摘要

背景

零聚体肽是天然蛋白质数据库中不存在的最小序列。我们于2006年首次开始编制缺失的5氨基酸序列清单(1)。我们在此报告零聚体衍生肽9R、9S1R和124R对NCI-60细胞系的影响,该细胞系源自9种器官(肾、卵巢、皮肤黑色素瘤、肺、脑、肺、结肠、前列腺和造血系统)的人类癌症,以及四种正常细胞系(内皮细胞HUVEC、皮肤成纤维细胞BJ、结肠上皮细胞FHC和正常前列腺细胞RWPE-1)。

方法

NCI-60癌细胞系和四种正常细胞系在补充有10% HyClone胎牛血清的RPMI1640培养基中体外培养,并分别用5 μM、25 μM和50 μM的肽9R、9S1R和124R处理48小时。通过CCK-8法评估细胞活力。为了研究肽对ATP的消耗作用,将NCI-60细胞系中代表每个器官的一种细胞系和四种正常细胞系用50 μM的肽9R、9S1R和124R处理3小时。评估全细胞及其上清液中的ATP含量。

结果

肽9S1R和9R分别对所测试的60种癌细胞系中的95%和81.6%具有致死性。对照肽124R对这些细胞的生长没有影响。特别有趣的是,肽9R和9S1R能够杀死耐药和激素抵抗细胞系,甚至癌症干细胞。肽9R和9S1R的活性谱比目前使用的许多癌症药物更广,能在3小时内完全耗尽细胞内的ATP,并且对所测试的4种正常细胞系中的3种的毒性低于对几种癌症的毒性。

结论

零聚体肽9R和9S1R对NCI-60细胞系中代表的9种器官来源的癌细胞系具有广泛的致死作用。这种广泛的活性跨越了癌症一般分类中使用的许多分类范畴:实体癌与液体癌、药物敏感与耐药、激素敏感与激素抵抗、细胞因子敏感与细胞因子不敏感、生长缓慢与生长迅速、分化癌与去分化癌。此外,肽9R和9S1R对癌症干细胞和乳腺肉瘤具有致死性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5926/5551024/ee3cc1ba4038/12885_2017_3514_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验