4.6 Article

Selection and Validation of Reference Genes for Pan-Cancer in Platelets Based on RNA-Sequence Data

期刊

FRONTIERS IN GENETICS
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2022.913886

关键词

platelets; reference genes; quantitative real time polymerase chain reaction; normalization; pan-cancer

资金

  1. Sichuan Provincial Cadre Health Research Project [2021-804]
  2. Health and Family Planning Commission of Sichuan Province universal application project [19PJ275, 20PJ115]
  3. Science and Technology Bureau of Chengdu technological innovation project [2019-YF05-01279-SN]
  4. Chengdu Science and Technology Bureau [2019-YF09-00034-CG]
  5. Science and Technology Department of Sichuan Province [2018JY0311, 2019JDRC0049]

向作者/读者索取更多资源

Many studies have shown that certain messenger RNA (mRNA) in platelets can serve as biomarkers for diagnosing pan-cancer. This study used bioinformatics and functional analysis to identify and validate reference genes for pan-cancer diagnosis based on platelet transcript analysis. The results confirmed that GAPDH gene was the most suitable reference gene for this purpose, providing a platform for molecular diagnosis of pan-cancer using platelets.
Many studies in recent years have demonstrated that some messenger RNA (mRNA) in platelets can be used as biomarkers for the diagnosis of pan-cancer. The quantitative real-time polymerase chain reaction (RT-qPCR) molecular technique is most commonly used to determine mRNA expression changes in platelets. Accurate and reliable relative RT-qPCR is highly dependent on reliable reference genes. However, there is no study to validate the reference gene in platelets for pan-cancer. Given that the expression of some commonly used reference genes is altered in certain conditions, selecting and verifying the most suitable reference gene for pan-cancer in platelets is necessary to diagnose early stage cancer. This study performed bioinformatics and functional analysis from the RNA-seq of platelets data set (GSE68086). We generated 95 candidate reference genes after the primary bioinformatics step. Seven reference genes (YWHAZ, GNAS, GAPDH, OAZ1, PTMA, B2M, and ACTB) were screened out among the 95 candidate reference genes from the data set of the platelets' transcriptome of pan-cancer and 73 commonly known reference genes. These candidate reference genes were verified by another platelets expression data set (GSE89843). Then, we used RT-qPCR to confirm the expression levels of these seven genes in pan-cancer patients and healthy individuals. These RT-qPCR results were analyzed using the internal stability analysis software programs (the comparative Delta CT method, geNorm, NormFinder, and BestKeeper) to rank the candidate genes in the order of decreasing stability. By contrast, the GAPDH gene was stably and constitutively expressed at high levels in all the tested samples. Therefore, GAPDH was recommended as the most suitable reference gene for platelet transcript analysis. In conclusion, our result may play an essential part in establishing a molecular diagnostic platform based on the platelets to diagnose pan-cancer.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据