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dc.citation.endPage 76 -
dc.citation.number 1 -
dc.citation.startPage 63 -
dc.citation.title CANCER CELL -
dc.citation.volume 23 -
dc.contributor.author Ryu, Seongho -
dc.contributor.author McDonnell, Kevin -
dc.contributor.author Choi, Hyejin -
dc.contributor.author Gao, Dingcheng -
dc.contributor.author Hahn, Mary -
dc.contributor.author Joshi, Natasha -
dc.contributor.author Park, Sun-Mi -
dc.contributor.author Catena, Raul -
dc.contributor.author Do, Yoonkyung -
dc.contributor.author Brazin, Jacqueline -
dc.contributor.author Vandat, Linda T. -
dc.contributor.author Silver, Randi B. -
dc.contributor.author Mittal, Vivek -
dc.date.accessioned 2023-12-22T04:17:28Z -
dc.date.available 2023-12-22T04:17:28Z -
dc.date.created 2013-06-10 -
dc.date.issued 2013-01 -
dc.description.abstract The progression of cancer to metastatic disease is a major cause of death. We identified miR-708 being transcriptionally repressed by polycomb repressor complex 2-induced H3K27 trimethylation in metastatic breast cancer. miR-708 targets the endoplasnnic reticulum protein neuronatin to decrease intracellular calcium level, resulting in reduction of activation of ERK and FAK, decreased cell migration, and impaired metastases. Ectopic expression of neuronatin refractory to suppression by miR-708 rescued cell migration and metastasis defects. In patients with breast cancer, miR-708 expression was decreased in lymph node and distal metastases, suggesting a metastasis-suppressive role. Our findings uncover a mechanistic role for miR-708 in metastasis and provide a rationale for developing nniR-708 as a therapeutic agent against metastatic breast cancer. -
dc.identifier.bibliographicCitation CANCER CELL, v.23, no.1, pp.63 - 76 -
dc.identifier.doi 10.1016/j.ccr.2012.11.019 -
dc.identifier.issn 1535-6108 -
dc.identifier.scopusid 2-s2.0-84872376809 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/2963 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84872376809 -
dc.identifier.wosid 000313759100008 -
dc.language 영어 -
dc.publisher CELL PRESS -
dc.title Suppression of miRNA-708 by Polycomb Group Promotes Metastases by Calcium-Induced Cell Migration -
dc.type Article -
dc.relation.journalWebOfScienceCategory Oncology; Cell Biology -
dc.relation.journalResearchArea Oncology; Cell Biology -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

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