Abstract
Although CBR3 Antisense RNA 1 (CBR3-AS1) has been characterized as an oncogenic long non-coding RNA (lncRNA) in several cancers, a recent study reported the downregulation of CBR3-AS1 in colorectal cancer (CRC). Therefore, we analyzed its role in CRC. CBR3-AS1 and microRNA-29a (miR-29a) expression in tissue samples from CRC patients were analyzed by RT-qPCR. The interaction between CBR3-AS1 and miR-29a was predicted by IntaRNA and validated by RNA pull-down assay. The location of CBR3-AS1 was analyzed by nuclear fractionation assay. CBR3-AS1 overexpression was performed to analyze its role in miR-29a expression. The roles of CBR3-AS1 and miR-29a in CRC cell migration and invasion were analyzed by Transwell assay. CBR3-AS1 was downregulated, and miR-29a was upregulated in CRC. CBR3-AS1 and miR-29a directly interacted with each other. CBR3-AS1 was localized in both nucleus and cytoplasm fractions. CBR3-AS1 overexpression failed to alter miR-29a expression but reduced its enhancing effects on cell invasion and migration. CBR3-AS1 is downregulated in CRC and inhibits miR-29a-mediated cell migration and invasion by sponging miR-29a.
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MY and WXC: manuscript writing, literature research and data analysis; HJL, LY: data analysis, experimental work and statistical analysis. MWT and YHL: literature research, project management and research design. All authors read and approved the final manuscript.
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12033_2021_444_MOESM1_ESM.tif
Supplemental Figure 1 CBR3-AS1 increased the accumulation of CDC42BPA (A) and B7-H3 (B) mRNA in CRC cells. (*p<0.05) (TIF 6355 kb)
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Yang, M., Chen, W., Liu, H. et al. Long Non-coding RNA CBR3 Antisense RNA 1 is Downregulated in Colorectal Cancer and Inhibits miR-29a-Mediated Cell Migration and Invasion. Mol Biotechnol 64, 773–779 (2022). https://doi.org/10.1007/s12033-021-00444-2
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DOI: https://doi.org/10.1007/s12033-021-00444-2