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通过慢病毒中的 shRNA 敲低 PROX1 可减少小细胞肺癌细胞系的增殖。

Proliferation of small cell lung cancer cell line reduced by knocking-down PROX1 via shRNA in lentivirus.

机构信息

DABT, Assistant Professor, Department of Pulmonary and Critical Care Medicine, College of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55902, USA.

出版信息

Anticancer Res. 2013 Aug;33(8):3169-75.

Abstract

The present study aimed to find whether PROX1 is expressed in small cell lung cancer (SCLC) cell lines, and whether PROX1 knockdown with shRNA via lentivirus resulted in decreased cell proliferation. SCLC cell lines H69, H82, H187 and H889 were selected for the study. PROX1 mRNA and protein levels were determined with real-time reverse-transcription polymerase chain reaction(RT-PCR) and western blot, respectively. The localization and distribution of PROX1 was mapped by immunocytochemistry with a specific antibody. Three pairs of shRNA were selected from a pool of shRNA pairs, and packaged into lentivirus particles to infect the above cell lines. The non-target sequence (NT) and a house-keeping gene, glyceraldehyde 3 phosphate dehydrogenase (GAPDH), were employed as controls. SCLC cell proliferation rates were measured with bromine deoxyuridine (BrdU) incorporation method. The results indicated levels of that PROX1 mRNA were detected in SCLC cell lines in the following rank order H69>H889>H187>H82. A similar profile for PROX1 protein expression was captured. The majority of PROX1 was concentrated at the cell nucleus. H69 was selected to represent the above SCLC cell lines. The PROX1 level in H69 cells was successfully reduced with shRNA lentivirus, and the cell proliferation rate of infected H69 cells was dramatically reduced by 20-50%. Hence, it is concluded that PROX1 expression in SCLC cell line is high, and can be reduced with shRNA lentivirus, thereby reducing the cell proliferation rate.

摘要

本研究旨在探讨 PROX1 是否在小细胞肺癌(SCLC)细胞系中表达,以及通过慢病毒介导的 shRNA 敲低 PROX1 是否会导致细胞增殖减少。选择 SCLC 细胞系 H69、H82、H187 和 H889 进行研究。使用实时逆转录聚合酶链反应(RT-PCR)和 Western blot 分别测定 PROX1 mRNA 和蛋白水平。通过免疫细胞化学用特异性抗体绘制 PROX1 的定位和分布。从一组 shRNA 中选择三对 shRNA,并包装成慢病毒颗粒感染上述细胞系。非靶向序列(NT)和管家基因甘油醛 3 磷酸脱氢酶(GAPDH)被用作对照。通过溴脱氧尿苷(BrdU)掺入法测量 SCLC 细胞的增殖率。结果表明,在 SCLC 细胞系中检测到 PROX1 mRNA 的水平按以下顺序排列:H69>H889>H187>H82。捕获到 PROX1 蛋白表达的相似图谱。大多数 PROX1 集中在细胞核内。选择 H69 来代表上述 SCLC 细胞系。用 shRNA 慢病毒成功降低了 H69 细胞中的 PROX1 水平,感染的 H69 细胞的增殖率降低了 20-50%。因此,结论是 SCLC 细胞系中 PROX1 的表达水平较高,并且可以通过 shRNA 慢病毒降低,从而降低细胞增殖率。

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