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环状RNA ciRS-7在三阴性乳腺癌中的表达及其对细胞侵袭和迁移的影响

Expression of Circular RNA ciRS-7 and Its Effect on Invasion and Migration of Triple-negative Breast Cancer Cells

  • 摘要:
    目的 探讨环状RNA ciRS-7在三阴性乳腺癌(TNBC)中的表达及其对细胞侵袭和迁移的影响。
    方法 通过qRT-PCR法检测乳腺癌组织和细胞中ciRS-7的表达水平,分析其与乳腺癌患者临床病理指标之间的关系。用划痕实验和Transwell实验检测沉默ciRS-7后MDA-MB-231和BT-549细胞的迁移和侵袭能力的变化。利用动物实验在体内进行验证。
    结果 TNBC组织中ciRS-7的相对表达量为(6.52±0.38),显著高于Luminal型(1.56±0.17)(P < 0.001)和HER2过表达型乳腺癌组织(2.27±0.66)(P < 0.001)以及癌旁正常组织(0.83±0.09)(P < 0.001)。ciRS-7表达与分子分型、肿瘤浸润和淋巴结转移明显相关(均P < 0.05);而与患者年龄、肿瘤直径和病理分级无关(均P > 0.05)。沉默ciRS-7后,MDA-MB-231和BT-549细胞的迁移和侵袭明显减弱(均P < 0.05)。ciRS-7敲低组肺转移瘤数明显减少(P < 0.05)。
    结论 ciRS-7在TNBC中高表达,并可能增强TNBC细胞的侵袭和迁移。

     

    Abstract:
    Objective To investigate the expression of circular RNA ciRS-7 in triple-negative breast cancer (TNBC) and its effect on invasion and migration.
    Methods The expression levels of ciRS-7 in TNBC tissues and cells were detected by qRT-PCR, and its relationship with clinicopathological parameters of breast cancer patients was further analyzed. Scratch and Transwell assays were used to detect the migration and invasion of MDA-MB-231 and BT-549 cells after silencing ciRS-7. Animal experiment was performed to verify the above findings in vivo.
    Results The relative expression of ciRS-7 in TNBC tissues was (6.52±0.38), significantly higher than Luminal type (1.56±0.17) (P < 0.001), HER2 overexpressing breast cancer tissues (2.27±0.66) (P < 0.001) and normal adjacent tissues (0.83 ± 0.09) (P < 0.001). Clinical data analysis showed that ciRS-7 expression was significantly associated with molecular typing, tumor invasion and lymph node metastasis (all P < 0.05), not associated with patients' age, tumor diameter or pathological grade (all P > 0.05). After silencing ciRS-7, the migration and invasion of MDA-MB-231 and BT-549 cells were significantly reduced (all P < 0.05). The number of lung metastasis clones was significantly reduced in ciRS-7 knockdown group (P < 0.05).
    Conclusion ciRS-7 is highly expressed in TNBC and may enhance the invasion and migration of TNBC cells.

     

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