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@article{1405392, author = {Vychytilová, Petra and Merhautová, Jana and Macháčková, Táňa and GutierrezandGarcia, Irene and GarciaandSolano, José and Radová, Lenka and Brchnelová, Dominika and Slabá, Kateřina and Svoboda, Marek and Halámková, Jana and Demlová, Regina and Kiss, Igor and Vyzula, Rostislav and ConesaandZamora, Pablo and Slabý, Ondřej}, article_location = {New York, USA}, article_number = {11}, doi = {http://dx.doi.org/10.1038/s41389-017-0006-6}, keywords = {miR-215; colorectal cancer; EGFR; proliferation; tumor suppressor; HOXB9; epiregulin}, language = {eng}, issn = {2157-9024}, journal = {Oncogenesis}, title = {MiR-215-5p is a tumor suppressor in colorectal cancer targeting EGFR ligand epiregulin and its transcriptional inducer HOXB9}, url = {https://www.nature.com/articles/s41389-017-0006-6}, volume = {6}, year = {2017} }
TY - JOUR ID - 1405392 AU - Vychytilová, Petra - Merhautová, Jana - Macháčková, Táňa - Gutierrez-Garcia, Irene - Garcia-Solano, José - Radová, Lenka - Brchnelová, Dominika - Slabá, Kateřina - Svoboda, Marek - Halámková, Jana - Demlová, Regina - Kiss, Igor - Vyzula, Rostislav - Conesa-Zamora, Pablo - Slabý, Ondřej PY - 2017 TI - MiR-215-5p is a tumor suppressor in colorectal cancer targeting EGFR ligand epiregulin and its transcriptional inducer HOXB9 JF - Oncogenesis VL - 6 IS - 11 SP - 399-412 EP - 399-412 PB - Nature publishing group SN - 21579024 KW - miR-215 KW - colorectal cancer KW - EGFR KW - proliferation KW - tumor suppressor KW - HOXB9 KW - epiregulin UR - https://www.nature.com/articles/s41389-017-0006-6 L2 - https://www.nature.com/articles/s41389-017-0006-6 N2 - Growing evidence suggests that microRNAs are involved in the development and progression of colorectal cancer (CRC). In the present study, deregulation and functioning of tumor-suppressive miR-215-5p was evaluated in CRC. In total, 448 tumor tissues and 325 paired adjacent healthy tissues collected from Czech and Spain cohorts of CRC patients have been used for miR-215-5p expression analyses. A series of in vitro experiments have been performed using transient transfection of miR-215-5p mimics into four CRC cell lines to identify specific cellular processes affected by miR-215-5p. Further, the effects of miR-215-5p on tumor growth were evaluated in vivo using NSG mice and stable cell line overexpressing miR-215-5p. Target mRNAs of miR-215-5p were tested using luciferase assay and western blot analyses. We found that miR-215-5p is significantly downregulated in tumor tissues compared with non-tumor adjacent tissues and its decreased levels correlate with the presence of lymph node metastases, tumor stage, and shorter overall survival in CRC patients. Overexpression of miR-215-5p significantly reduced proliferation, clonogenicity, and migration of CRC cells, lead to cell cycle arrest in G2/M phase and p53-dependent induction of apoptosis. The ability of miR-215-5p to inhibit tumor growth was confirmed in vivo. Finally, we confirmed epiregulin and HOXB9 to be the direct targets of miR-215-5p. As epiregulin is EGFR ligand and HOXB9 is its transcriptional inducer, we suggest that the main molecular link between miR-215-5p and CRC cells phenotypes presents the EGFR signaling pathway, which is one of the canonical pathogenic pathways in CRC. ER -
VYCHYTILOVÁ, Petra, Jana MERHAUTOVÁ, Táňa MACHÁČKOVÁ, Irene GUTIERREZ-GARCIA, José GARCIA-SOLANO, Lenka RADOVÁ, Dominika BRCHNELOVÁ, Kateřina SLABÁ, Marek SVOBODA, Jana HALÁMKOVÁ, Regina DEMLOVÁ, Igor KISS, Rostislav VYZULA, Pablo CONESA-ZAMORA and Ondřej SLABÝ. MiR-215-5p is a tumor suppressor in colorectal cancer targeting EGFR ligand epiregulin and its transcriptional inducer HOXB9. \textit{Oncogenesis}. New York, USA: Nature publishing group, 2017, vol.~6, No~11, p.~399-412. ISSN~2157-9024. Available from: https://dx.doi.org/10.1038/s41389-017-0006-6.
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