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Zinc finger protein 143 expression is closely related to tumor malignancy via regulating cell motility in breast cancer

机译:锌指蛋白143的表达通过调节乳腺癌细胞的运动性与肿瘤恶性程度密切相关

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摘要

We previously reported the involvement of zinc-finger protein 143 (ZNF143) on cancer cell motility in colon cancer cells. Here, ZNF143 was further characterized in breast cancer. Immunohistochemistry was used to determine the expression of ZNF143 in normal tissues and in tissues from metastatic breast cancer at various stages. Notably, ZNF143 was selectively expressed in duct and gland epithelium of normal breast tissues, which decreased when the tissue became malignant. To determine the molecular mechanism how ZNF143 affects breast cancer progression, it was knocked down by infecting benign breast cancer cells with short-hairpin (sh) RNA-lentiviral particles against ZNF143 (MCF7 sh-ZNF143). MCF7 sh-ZNF143 cells showed different cell-cell contacts and actin filament (F-actin) structures when compared with MCF7 sh-Control cells. In migration and invasion assays, ZNF143 knockdown induced increased cellular motility in breast carcinoma cells. This was reduced by the recovery of ZNF143 expression. Taken together, these results suggest that ZNF143 expression contributes to breast cancer progression.
机译:我们先前曾报道锌指蛋白143(ZNF143)与结肠癌细胞的癌细胞运动有关。在这里,ZNF143在乳腺癌中具有进一步的特征。免疫组织化学用于确定ZNF143在正常组织和转移性乳腺癌组织不同阶段的表达。值得注意的是,ZNF143在正常乳腺组织的导管和腺上皮中选择性表达,当组织变为恶性肿瘤时ZNF143减少。为了确定ZNF143如何影响乳腺癌进展的分子机制,通过使用针对ZNF143(MCF7 sh-ZNF143)的短发夹(sh)RNA-慢病毒颗粒感染良性乳腺癌细胞来将ZNF143敲低。与MCF7 sh-Control细胞相比,MCF7 sh-ZNF143细胞显示出不同的细胞间接触和肌动蛋白丝(F-actin)结构。在迁移和侵袭试验中,ZNF143敲低诱导乳腺癌细胞的细胞运动性增加。 ZNF143表达的恢复减少了这种情况。综上,这些结果表明ZNF143的表达有助于乳腺癌的进展。

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