Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2407-12-232
Title: MicroRNA-143 down-regulates Hexokinase 2 in colon cancer cells
Authors: Gregersen, L.H
Jacobsen, A 
Frankel, L.B
Wen, J
Krogh, A
Lund, A.H
Keywords: glucose
hexokinase
lactic acid
microRNA 143
protein HK2
unclassified drug
3' untranslated region
anaerobic glycolysis
article
cancer cell culture
colon cancer
colon carcinogenesis
controlled study
down regulation
enzyme release
gene overexpression
glucose metabolism
human
human cell
microarray analysis
protein depletion
protein targeting
Cell Line, Tumor
Cell Proliferation
Colonic Neoplasms
Down-Regulation
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Hexokinase
Humans
MicroRNAs
RNA Interference
Signal Transduction
Issue Date: 2012
Citation: Gregersen, L.H, Jacobsen, A, Frankel, L.B, Wen, J, Krogh, A, Lund, A.H (2012). MicroRNA-143 down-regulates Hexokinase 2 in colon cancer cells. BMC Cancer 12 : 232. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2407-12-232
Rights: Attribution 4.0 International
Abstract: Background: MicroRNAs (miRNAs) are well recognized as gene regulators and have been implicated in the regulation of development as well as human diseases. miR-143 is located at a fragile site on chromosome 5 frequently deleted in cancer, and has been reported to be down-regulated in several cancers including colon cancer.Methods: To gain insight into the role of miR-143 in colon cancer, we used a microarray-based approach in combination with seed site enrichment analysis to identify miR-143 targets.Results: As expected, transcripts down-regulated upon miR-143 overexpression had a significant enrichment of miR-143 seed sites in their 3'UTRs. Here we report the identification of Hexokinase 2 (HK2) as a direct target of miR-143. We show that re-introduction of miR-143 in the colon cancer cell line DLD-1 results in a decreased lactate secretion.Conclusion: We have identified and validated HK2 as a miR-143 target. Furthermore, our results indicate that miR-143 mediated down-regulation of HK2 affects glucose metabolism in colon cancer cells. We hypothesize that loss of miR-143-mediated repression of HK2 can promote glucose metabolism in cancer cells, contributing to the shift towards aerobic glycolysis observed in many tumors. © 2012 Gregersen et al.; licensee BioMed Central Ltd.
Source Title: BMC Cancer
URI: https://scholarbank.nus.edu.sg/handle/10635/181607
ISSN: 14712407
DOI: 10.1186/1471-2407-12-232
Rights: Attribution 4.0 International
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