PROTAC: A promising technology for cancer treatment
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Authors: Zhou, Xin; Dong, Ru; Zhang, Jin-Yang; Zheng, Xin; Sun, Li-Ping
Abstract
Proteolysis-targeting chimeric molecules (PROTACs), which attract much more attention today, may be a potential way to treat cancer. PROTACs are made up of ligands of target proteins, E3 ligase recruiting elements and linkers. PROTACs can hijack the intracellular inherent ubiquitin proteasome system in cells to degrade different target proteins. PROTACs targeting different cancer-related proteins have been successfully developed and outperform small inhibitors, the traditional way of treating cancer. In this review, we focus on PROTACs targeting cancer-related proteins and their superiority over inhibitors. (C) 2020 Elsevier Masson SAS. All rights reserved.
Evaluation of duplicated reference genes for quantitative real-time PCR analysis in genome unknown hexaploid oat (Avena sativaL.)
PLANT METHODS
Authors: Yang, Zheng; Wang, Kai; Aziz, Usman; Zhao, Cuizhu; Zhang, Meng
Abstract
Background Oat (Avena sativaL.), a hexaploid crop with unknown genome, has valuable nutritional, medicinal and pharmaceutical uses. However, no suitable RGs (reference genes) for qPCR (quantitative real-time PCR) has been documented for oat yet. Single-copy gene is often selected as RG, which is challengeable or impactable in unexplored polyploids. Results In this study, eleven candidate RGs, including four duplicated genes, were selected from oat transcriptome. The stability and the optimal combination of these candidate RGs were assessed in 18 oat samples by using four statistical algorithms including the Delta Ct method, geNorm, NormFinder and BestKeeper. The most stable RGs for "all samples", "shoots and roots of seedlings", "developing seeds" and "developing endosperms" wereEIF4A(Eukaryotic initiation factor 4A-3),UBC21(Ubiquitin-Conjugating Enzyme 21),EP(Expressed protein) andEIF4Arespectively. Among these RGs,UBC21was a four-copy duplicated gene. The reliability was validated by the expression patterns of four various genes normalized to the most and the least stable RGs in different sample sets. Conclusions Results provide a proof of concept that the duplicated RG is feasible for qPCR in polyploids. To our knowledge, this study is the first systematic research on the optimal RGs for accurate qPCR normalization of gene expression in different organs and tissues of oat.