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Ovarian Cancer Stem Cells with High ROR1 Expression Serve as a New Prophylactic Vaccine for Ovarian Cancer

机译:ROR1高表达的卵巢癌干细胞作为卵巢癌的新型预防疫苗。

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摘要

Tumor vaccines offer a number of advantages for cancer treatment. In the study, the vaccination with cancer stem cells (CSCs) with high expression of the type I receptor tyrosine kinase-like orphan receptor (ROR1) was evaluated in a murine model for the vaccine's immunogenicity and protective efficacy against epithelial ovarian carcinoma (EOC). CD117+CD44+ CSCs were isolated from human EOC HO8910 cell line using a magnetic-activated cell sorting system; murine ID8 EOC suspension sphere cells, which are collectively known as cancer stem-like cells, were acquired from serum-free suspension sphere-forming culture. Mice were subcutaneously immunized with the repeat cycles of freezing and thawing whole HO8910 CD117+CD44+ CSCs and ID8 cancer stem-like cells, respectively, followed by a challenge with HO8910 or ID8 cells at one week after final vaccination. The results showed that the CSC vaccination significantly induced immunity against EOC growth and markedly prolonged the survival of EOC-bearing mice in the prophylactic setting compared with non-CSC vaccination. Flow cytometry showed significantly increased immunocyte cytotoxicities and remarkably reduced CSC counts in the CSC-vaccinated mice. Moreover, the protective efficacy against EOC was decreased when the ROR1 expression was downregulated by shRNA in CSC vaccines. The findings from the study suggest that CSC vaccines with high ROR1 expression were highly effective in triggering immunity against EOC in vaccinated mice and may serve as an effective vaccine for EOC immunoprophylaxis.
机译:肿瘤疫苗为癌症治疗提供了许多优势。在这项研究中,在鼠模型中评估了具有高表达I型受体酪氨酸激酶样孤儿受体(ROR1)的癌症干细胞(CSC)的疫苗接种疫苗的免疫原性和针对上皮性卵巢癌(EOC)的保护功效。使用磁激活细胞分选系统从人EOC HO8910细胞系中分离出CD117 + CD44 + CSC。从无血清悬浮球形成培养物中获得了鼠类ID8 EOC悬浮球细胞,这些细胞统称为癌症干细胞样细胞。分别重复冷冻和融化整个HO8910 CD117 + CD44 + CSCs和ID8癌干样细胞的重复循环,对小鼠进行皮下免疫,然后用HO8910或最终疫苗接种后第一个星期的ID8细胞。结果表明,与非CSC疫苗接种相比,CSC疫苗接种显着诱导了针对EOC生长的免疫力,并在预防环境中显着延长了带有EOC的小鼠的存活期。流式细胞术显示,在接种CSC的小鼠中,免疫细胞的细胞毒性显着增加,CSC计数显着降低。此外,当CSC疫苗中ROR1表达被shRNA下调时,对EOC的保护作用降低。该研究的发现表明,具有高ROR1表达的CSC疫苗可有效触发疫苗接种小鼠中的EOC免疫力,并可作为EOC免疫预防的有效疫苗。

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