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人胰腺癌样本、相邻正常组织以及源自这些肿瘤的异种移植瘤之间特定微小RNA(miRNA)水平及其潜在蛋白质靶点的变化。

Alteration in Levels of Specific miRNAs and Their Potential Protein Targets between Human Pancreatic Cancer Samples, Adjacent Normal Tissue, and Xenografts Derived from These Tumors.

作者信息

O'Neill Fiona, Allen-Coyle Taylor-Jade, Roche Sandra, Meiller Justine, Conlon Neil T, Swan Niall, Straubinger Robert M, Geoghegan Justin, Straubinger Ninfa L, Conlon Kevin, McDermott Ray, O'Sullivan Finbarr, Henry Michael, Meleady Paula, McVey Gerard, O'Connor Robert, Moriarty Michael, Clynes Martin

机构信息

National Institute for Cellular Biotechnology, Dublin City University, D09 NR58 Dublin, Ireland.

SSPC, The Science Foundation Ireland Research Centre for Pharmaceuticals, V94 T9PX Limerick, Ireland.

出版信息

Life (Basel). 2023 Feb 22;13(3):608. doi: 10.3390/life13030608.

Abstract

Herein, we describe the global comparison of miRNAs in human pancreatic cancer tumors, adjacent normal tissue, and matched patient-derived xenograft models using microarray screening. RNA was extracted from seven tumor, five adjacent normal, and eight FI PDX tumor samples and analyzed by Affymetrix GeneChip miRNA 4.0 array. A transcriptome analysis console (TAC) was used to generate comparative lists of up- and downregulated miRNAs for the comparisons, tumor vs. normal and F1 PDX vs. tumor. Particular attention was paid to miRNAs that were changed in the same direction in both comparisons. We identified the involvement in pancreatic tumor tissue of several miRNAs, including miR4534, miR3154, and miR4742, not previously highlighted as being involved in this type of cancer. Investigation in the parallel mRNA and protein lists from the same samples allowed the elimination of proteins where altered expression correlated with corresponding mRNA levels and was thus less likely to be miRNA regulated. Using the remaining differential expression protein lists for proteins predicted to be targeted for differentially expressed miRNA on our list, we were able to tentatively ascribe specific protein changes to individual miRNA. Particularly interesting target proteins for miRs 615-3p, 2467-3p, 4742-5p, 509-5p, and 605-3p were identified. Prominent among the protein targets are enzymes involved in aldehyde metabolism and membrane transport and trafficking. These results may help to uncover vulnerabilities that could enable novel approaches to treating pancreatic cancer.

摘要

在此,我们描述了通过微阵列筛选对人类胰腺癌肿瘤、癌旁正常组织以及匹配的患者来源异种移植模型中的微小RNA(miRNA)进行的全面比较。从7个肿瘤样本、5个癌旁正常样本和8个F1 PDX肿瘤样本中提取RNA,并通过Affymetrix GeneChip miRNA 4.0阵列进行分析。使用转录组分析控制台(TAC)生成上调和下调miRNA的比较列表,用于肿瘤与正常组织以及F1 PDX与肿瘤的比较。特别关注在两种比较中方向相同的miRNA。我们确定了几种miRNA参与胰腺肿瘤组织,包括miR4534、miR3154和miR4742,这些miRNA之前未被强调与这类癌症有关。对相同样本的平行mRNA和蛋白质列表进行研究,使得与相应mRNA水平相关的表达改变的蛋白质被排除,因此这些蛋白质不太可能受miRNA调控。利用剩余的差异表达蛋白质列表,针对我们列表中预测为差异表达miRNA靶向的蛋白质,我们能够初步将特定的蛋白质变化归因于单个miRNA。确定了miR 615 - 3p、miR 2467 - 3p、miR 4742 - 5p、miR 509 - 5p和miR 605 - 3p特别有趣的靶蛋白。在蛋白质靶标中突出的是参与醛代谢以及膜转运和运输的酶。这些结果可能有助于揭示潜在的薄弱环节,从而为治疗胰腺癌开辟新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64f9/10057657/6b54c18ead36/life-13-00608-g001.jpg

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