Crown Biosciences Inc, Science & Technology Innovation Park, Taicang, China.
Elife. 2019 Mar 12;8:e43511. doi: 10.7554/eLife.43511.
As part of the Reproducibility Project: Cancer Biology, we published a Registered Report (Li et al., 2015), that described how we intended to replicate selected experiments from the paper 'The microRNA miR-34a inhibits prostate cancer stem cells and metastasis by directly repressing CD44' (Liu et al., 2011). Here we report the results. We found the microRNA, miR-34a, was expressed at twice the level in CD44 prostate cancer cells purified from xenograft tumors (LAPC4 cells) compared to CD44 LAPC4 cells, whereas the original study reported miR-34a was underexpressed in CD44 LAPC4 cells (Figure 1B; Liu et al., 2011). When LAPC4 cells engineered to express miR-34a were injected into mice, we did not observe changes in tumor growth or CD44 expression; however, unexpectedly miR-34a expression was lost . In the original study, LAPC4 cells expressing miR-34a had a statistically significant reduction in tumor regeneration and reduced CD44 expression compared to control (Figure 4A and Supplemental Figures 4A,B and 5C; Liu et al., 2011). Furthermore, when we tested if miR-34a regulated CD44 through binding sites in the 3'UTR we did not find a statistically significant difference, whereas the original study reported miR-34a decreased CD44 expression that was partially abrogated by mutation of the binding sites in the 3'UTR (Figure 4D; Liu et al., 2011). Finally, where possible, we report meta-analyses for each result.
癌症生物学的一部分,我们发表了一份已注册的报告(Li 等人,2015 年),其中描述了我们如何打算复制论文“microRNA miR-34a 通过直接抑制 CD44 抑制前列腺癌干细胞和转移”(Liu 等人,2011 年)中的选定实验。在这里,我们报告结果。我们发现,在源自异种移植肿瘤的 CD44 前列腺癌细胞(LAPC4 细胞)中,microRNA miR-34a 的表达水平是 CD44 LAPC4 细胞的两倍,而原始研究报告 miR-34a 在 CD44 LAPC4 细胞中表达不足(图 1B;Liu 等人,2011 年)。当表达 miR-34a 的 LAPC4 细胞被注射到小鼠中时,我们没有观察到肿瘤生长或 CD44 表达的变化;然而,出人意料的是,miR-34a 的表达丢失了。在原始研究中,与对照相比,表达 miR-34a 的 LAPC4 细胞的肿瘤再生和 CD44 表达明显减少(图 4A 和补充图 4A、B 和 5C;Liu 等人,2011 年)。此外,当我们测试 miR-34a 是否通过 3'UTR 中的结合位点调节 CD44 时,我们没有发现统计学上的显著差异,而原始研究报告说 miR-34a 降低了 CD44 的表达,这种表达被 3'UTR 中的结合位点突变部分阻断(图 4D;Liu 等人,2011 年)。最后,在可能的情况下,我们报告了每个结果的荟萃分析。