MicroRNA-182 drives metastasis of primary sarcomas by targeting multiple genes.

Journal Article (Journal Article)

Metastasis causes most cancer deaths, but is incompletely understood. MicroRNAs can regulate metastasis, but it is not known whether a single miRNA can regulate metastasis in primary cancer models in vivo. We compared the expression of miRNAs in metastatic and nonmetastatic primary mouse sarcomas and found that microRNA-182 (miR-182) was markedly overexpressed in some tumors that metastasized to the lungs. By utilizing genetically engineered mice with either deletion of or overexpression of miR-182 in primary sarcomas, we discovered that deletion of miR-182 substantially decreased, while overexpression of miR-182 considerably increased, the rate of lung metastasis after amputation of the tumor-bearing limb. Additionally, deletion of miR-182 decreased circulating tumor cells (CTCs), while overexpression of miR-182 increased CTCs, suggesting that miR-182 regulates intravasation of cancer cells into the circulation. We identified 4 miR-182 targets that inhibit either the migration of tumor cells or the degradation of the extracellular matrix. Notably, restoration of any of these targets in isolation did not alter the metastatic potential of sarcoma cells injected orthotopically, but the simultaneous restoration of all 4 targets together substantially decreased the number of metastases. These results demonstrate that a single miRNA can regulate metastasis of primary tumors in vivo by coordinated regulation of multiple genes.

Full Text

Duke Authors

Cited Authors

  • Sachdeva, M; Mito, JK; Lee, C-L; Zhang, M; Li, Z; Dodd, RD; Cason, D; Luo, L; Ma, Y; Van Mater, D; Gladdy, R; Lev, DC; Cardona, DM; Kirsch, DG

Published Date

  • October 2014

Published In

Volume / Issue

  • 124 / 10

Start / End Page

  • 4305 - 4319

PubMed ID

  • 25180607

Pubmed Central ID

  • PMC4191039

Electronic International Standard Serial Number (EISSN)

  • 1558-8238

Digital Object Identifier (DOI)

  • 10.1172/JCI77116


  • eng

Conference Location

  • United States