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Circular RNA circPLK1 promotes breast cancer cell proliferation migration and invasion by regulating miR-4500/IGF1 axis

机译:圆形RNA循环通过调节miR-4500 / IGF1轴来促进乳腺癌细胞增殖迁移和侵袭

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摘要

CircPLK1 expression was enhanced in BC tissues and cells. a The expression of circPLK1 was detected by qRT-PCR in 35 pairs of BC tissues and adjacent normal tissues. b ΔΔct is the difference between the ΔCT of BC tissues and the ΔCT of adjacent normal tissues. Relative circPLK1 expression in BC tissues (n = 35) compared with corresponding non-tumor tissues (n = 35). Positive − ΔΔct meant high circPLK1 expression. Negative − ΔΔct meant low circPLK1 expression. c CircPLK1 expression was determined by qRT-PCR in BC cells (BT549 and HCC38) and MCF-10A cells. d The relative levels of circPLK1 and PLK1 mRNA were measured after treatment with RNase R by qRT-PCR. e Relative RNA levels of circPLK1 and PLK1 mRNA were detected after reverse transcription with random primers and Oligo (dT) 18 primers by qRT-PCR. ***P < 0.001
机译:在BC组织和细胞中,Circlk1表达增强。 QRT-PCR在35对BC组织和相邻的正常组织中检测到循环循环表达。 BΔΔCt是BC组织的ΔCt与相邻正常组织的ΔCt之间的差异。与相应的非肿瘤组织(n = 35)相比,BC组织中的相对循环表达(n = 35)。正 - ΔΔct意味着高循环型表达。负 - ΔΔCt意味着低循环循环表达。 C循环循环表达由BC细胞(BT549和HCC38)和MCF-10A细胞中的QRT-PCR测定。 d通过QRT-PCR处理后测量Circlk1和PLK1 mRNA的相对水平。通过通过QRT-PCR逆转随机引物和寡核苷酸(DT)18引物在逆转转录后检测e相对RNA水平。 *** p <0.001

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