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Targeted inhibition of long non-coding RNA H19 blocks anaplastic thyroid carcinoma growth and metastasis

机译:靶向抑制长期非编码RNA H19阻断血管塑性甲状腺癌生长和转移

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摘要

Long non-coding RNA H19 (H19) is highly expressed in cancers and is considered to highly correlate with the extent of malignant degree. The present study was performed to determine the expression levels of H19 in anaplastic thyroid carcinoma (ATC) tissues and the role of H19 in ATC 8505C cells in vitro and in vivo. Expression of H19 was detected in 19 ATC and 19 normal thyroid tissues by real-time quantitative polymerase chain reaction. Utilizing the siRNA or short hairpin RNA (shRNA) directed against human H19 (H19 siRNA or shRNA H19) depleted H19 in ATC 8505C cells and characterized the outcomes. The results showed that H19 was overexpressed in ATC tissues. Targeting H19 inhibited proliferation, migration, and invasion and induced apoptosis in 8505C cells in vitro and inhibited tumorigenesis and metastasis in vivo. Therefore, the H19 might be an effective target for ATC molecular therapy.
机译:长期非编码RNA H19(H19)在癌症中高度表达,被认为与恶性程度的程度高度相关。进行本研究以确定在体外和体内H19在ATC 8505C细胞中H19中的H19中H19的表达水平。通过实时定量聚合酶链反应在19个ATC和19正常甲状腺组织中检测H19的表达。利用针对人H19(H19 siRNA或ShRNA H19)的siRNA或短发夹RNA(ShRNA)在ATC 8505C细胞中耗尽H19并表征结果。结果表明,H19在ATC组织中过表达。靶向H19在体外抑制8505℃细胞中的增殖,迁移和侵袭和诱导细胞凋亡,抑制体内肿瘤内酯和转移。因此,H19可能是ATC分子疗法的有效靶标。

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