| Literature DB >> 27692896 |
Tairong Kuang1, Lingqian Chang2, Xiangfang Peng3, Xianglong Hu4, Daniel Gallego-Perez5.
Abstract
Heterogeneities and oncogenesis essentially result from proteomic disorders orchestrated by changes in DNA and/or cytoplasmic mRNA. These genetic fluctuations, however, cannot be decoded through conventional label-free methods (e.g., patch clamps, electrochemical cellular biosensors, etc.) or morphological characterization. Molecular beacons (MBs) have recently emerged as efficient probes for interrogating biomarkers in live cancer cells. MBs hybridize with their intracellular targets (e.g., mRNAs, DNAs, or proteins), emitting a fluorescent signal that can be quantified and correlated with the expression levels of their targets. In this review we discuss MB probes with different delivery platforms for intracellular probing as well as novel MB designs for detecting a variety of targets in living cancer cells. Finally, we describe current trends in MB-based intracellular biosensors.Entities:
Keywords: cancer cells; heterogeneities; intracellular delivery; intracellular probes; mRNAs; molecular beacons
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Year: 2016 PMID: 27692896 DOI: 10.1016/j.tibtech.2016.09.003
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536