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Effects of thymosin β4-derived peptides on migration and invasion of ovarian cancer cells
Genes & Genomics ( IF 1.6 ) Pub Date : 2021-06-25 , DOI: 10.1007/s13258-021-01127-7
Hyung Joon Yoon 1 , Young Lim Oh 2 , Eun-Ji Ko 3 , Ahyun Kang 4 , Wan Kyu Eo 5 , Ki Hyung Kim 6 , Ji Young Lee 7 , Ari Kim 8 , Sungwook Chun 9 , Hongbae Kim 10 , Mee Sun Ock 3 , Hee-Jae Cha 3
Affiliation  

Background

Thymosin β4 (Tβ4) is a highly conserved actin binding protein associated with the metastatic potential of tumor cells by stimulating cell migration. The role of Tβ4 and its derived fragment peptides in migration of ovarian cancer cells has not been studied.

Objective

To analyze the effects of Tβ4 and its derived fragment peptides on ovarian cancer cell migration and invasion, we applied Tβ4 and three Tβ4-derived synthetic peptides to SKOV3 ovarian cancer cells.

Method

The migration and invasion of SKOV3 cells treated with Tβ4(1–43), Tβ4(1–15), Tβ4(12–26), Tβ4(23–), and untreated control were analyzed by in vitro migration and invasion assay with transwell plate. Cell proliferation assay was conducted to identify the effect of Tβ4 and its derived peptide on SKOV3 cell proliferation. The expression of Tβ4 related proteins related with cell proliferation was analyzed by Western blot after treatment with Tβ4 and its derived peptides.

Results

Cell migration and invasion were significantly increased in Tβ4 peptide-treated SKOV3 cells compared with untreated control. All three Tβ4-derived fragment peptides including those without an actin binding site significantly stimulated migration and invasion of SKOV3 cells. Tβ4 and its derived peptide significantly stimulated SKOV3 cell proliferation and up-regulated the expression of RACK-1 protein.

Conclusions

The Tβ4 peptide and all of its derived fragment peptides including those without an actin binding motif stimulate migration and invasion of SKOV3 ovarian cancer cells. All peptides significantly increased RACK-1 expression and cell proliferation of SKOV3 cells. These results suggest that Tβ4 stimulates migration and invasion of SKOV3 cells by stimulation of cell proliferation through up-regulation of RACK-1 protein.



中文翻译:

胸腺素β4衍生肽对卵巢癌细胞迁移和侵袭的影响

背景

胸腺素 β4 (Tβ4) 是一种高度保守的肌动蛋白结合蛋白,通过刺激细胞迁移与肿瘤细胞的转移潜能相关。尚未研究 Tβ4 及其衍生片段肽在卵巢癌细胞迁移中的作用。

客观的

为了分析 Tβ4 及其衍生片段肽对卵巢癌细胞迁移和侵袭的影响,我们将 Tβ4 和三种 Tβ4 衍生的合成肽应用于 SKOV3 卵巢癌细胞。

方法

用 transwell 的体外迁移和侵袭试验分析了用 Tβ4(1-43)、Tβ4(1-15)、Tβ4(12-26)、Tβ4(23-) 和未处理对照处理的 SKOV3 细胞的迁移和侵袭。盘子。进行细胞增殖测定以鉴定Tβ4及其衍生肽对SKOV3细胞增殖的影响。在用Tβ4及其衍生肽处理后,通过Western印迹分析与细胞增殖相关的Tβ4相关蛋白的表达。

结果

与未处理的对照相比,Tβ4 肽处理的 SKOV3 细胞中的细胞迁移和侵袭显着增加。所有三种 Tβ4 衍生的片段肽,包括那些没有肌动蛋白结合位点的肽,都显着刺激了 SKOV3 细胞的迁移和侵袭。Tβ4及其衍生肽显着刺激SKOV3细胞增殖并上调RACK-1蛋白的表达。

结论

Tβ4 肽及其所有衍生的片段肽,包括那些没有肌动蛋白结合基序的肽,可刺激 SKOV3 卵巢癌细胞的迁移和侵袭。所有肽均显着增加了 SKOV3 细胞的 RACK-1 表达和细胞增殖。这些结果表明Tβ4通过上调RACK-1蛋白刺激细胞增殖来刺激SKOV3细胞的迁移和侵袭。

更新日期:2021-06-25
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