4.3 Article

Gli1 enhances migration and invasion via up-regulation of MMP-11 and promotes metastasis in ERα negative breast cancer cell lines

Journal

CLINICAL & EXPERIMENTAL METASTASIS
Volume 28, Issue 5, Pages 437-449

Publisher

SPRINGER
DOI: 10.1007/s10585-011-9382-z

Keywords

Breast cancer; Gli1; Gli-mediated transcription; MMP-11; Invasion; Migration; Metastasis

Categories

Funding

  1. American Cancer Society [RSG-05-207-01-TBE]
  2. Susan G. Komen Foundation [BCTR0707453]
  3. National Institutes of Health [1R03CA130057]
  4. Department of Defense [BC083907]
  5. National Foundation for Cancer Research

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Gli1 is an established oncogene and its expression in Estrogen Receptor (ER) alpha negative and triple negative breast cancers is predictive of a poor prognosis; however, the biological functions regulated by Gli1 in breast cancer have not been extensively evaluated. Herein, Gli1 was over-expressed or down-regulated (by RNA interference and by expression of the repressor form of Gli3) in the ER alpha negative, human breast cancer cell lines MDA-MB-231 and SUM1315. Reduced expression of Gli1 in these two cell lines resulted in a decrease in migration and invasion. Gli1 over-expression increased the migration and invasion of MDA-MB-231 cells with a corresponding increase in expression of MMP-11. Silencing MMP-11 in MDA-MB-231 cells that over-expressed Gli1 abrogated the Gli1-induced enhancement of migration and invasion. Sustained suppression of Gli1 expression decreased growth of MDA-MB-231 in vitro by increasing apoptosis and decreasing proliferation. In addition, silencing of Gli1 reduced the numbers and sizes of pulmonary metastases of MDA-MB-231 in an in vivo experimental metastasis assay. In summary, Gli1 promotes the growth, survival, migration, invasion and metastasis of ER alpha negative breast cancer. Additionally, MMP-11 is up-regulated by Gli1 and mediates the migration and invasion induced by Gli1 in MDA-MB-231.

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