microRNAs can play a job in most cancers improvement and are thought to solely suppress protein expression in dividing cells, reminiscent of tumor cells. But new analysis printed in ACS Central Science reveals that a few of these tiny molecules can elevate the expression of a selected gene in dividing human cells and in most cancers cells, difficult typical knowledge.
Only just a few nucleotides in size, microRNAs, or miRNAs for brief, do not encode proteins. Instead, they largely downregulate, or suppress, protein manufacturing by silencing the expression of sure genes. One class of mobile equipment regulated by miRNAs are the enzymes concerned in mediating glycosylation, which add carbohydrates to sure proteins. In most cancers cells, nevertheless, this course of will be extremely dysregulated, suggesting that miRNAs might be doing one thing uncommon. So, Lara Mahal and colleagues got down to examine precisely how miRNAs perform inside the glycosylation course of, and whether or not the molecules could be functioning in a brand new manner.
Previously, the researchers developed a fluorescence assay that may analyze how miRNAs work together with their targets, and whether or not they improve or lower the quantity of protein produced. They used the assay to analyze the regulation of cancer-related glycosylation enzymes ST6GAL1 and ST6GAL2, and located that for the previous, the miRNAs appeared to immediately upregulate the method in noncancerous human cells. This challenges the present understanding that miRNAs solely downregulate protein manufacturing. They additionally examined for miRNA-mediated upregulation in a number of most cancers cell traces and noticed the identical outcomes. The researchers say that this work expands the understanding of how miRNAs work, an vital consideration for utilizing miRNA-based therapeutics in each present and future medical trials.
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Journal reference:
Jame-Chenarboo, F., et al. (2022) High-Throughput Analysis Reveals miRNA Upregulating α-2,6-Sialic Acid by Direct miRNA–mRNA Interactions. ACS Central Science. doi.org/10.1021/acscentsci.2c00748.