Loss of plakoglobin promotes decreased cell-cell contact, increased invasion, and breast cancer cell dissemination in vivo

• Published in: Breast cancer research : BCR 2012-05, Vol.14 (3), p.R86-R86, Article 3000
• Main Authors: Holen, Ingunn, Whitworth, Jacob, Nutter, Faith, Evans, Alyson, Brown, Hannah K, Lefley, Diane V, Barbaric, Ivana, Jones, Mark, Ottewell, Penelope D
• Format: Article
• Language: English
• Subjects: Animals; Breast cancer; Cell Adhesion; Cell adhesion molecules; Cell Communication; Cell Line, Tumor; Cell Movement; Cell Proliferation; Comparative analysis; Development and progression; Female; gamma Catenin - genetics; gamma Catenin - metabolism; Gene Expression Regulation, Neoplastic; Genetic vectors; Humans; Mammary Neoplasms, Animal - genetics; Mammary Neoplasms, Animal - metabolism; Mammary Neoplasms, Animal - pathology; MCF-7 Cells; Metastasis; Mice; Mice, Inbred BALB C; MicroRNA; Neoplasm Invasiveness; Neoplastic Cells, Circulating; Physiological aspects; RNA Interference; RNA, Small Interfering
• ISSN: 1465-542X; 1465-5411; 1465-542X
• DOI: 10.1186/bcr3201

The majority of deaths from breast cancer are a result of metastases; however, little is understood about the genetic alterations underlying their onset. Genetic profiling has identified the adhesion molecule plakoglobin as being three-fold reduced in expression in primary breast tumors that have metastasized compared with nonmetastatic tumors. In this study, we demonstrate a functional role for plakoglobin in the shedding of tumor cells from the primary site into the circulation. We investigated the effects of plakoglobin knockdown on breast cancer cell proliferation, migration, adhesion, and invasion in vitro and on tumor growth and intravasation in vivo. MCF7 and T47D cells were stably transfected with miRNA sequences targeting the plakoglobin gene, or scramble vector. Gene and protein expression was monitored by quantitative polymerase chain reaction (qPCR) and Western blot. Cell proliferation, adhesion, migration, and invasion were measured by cell counting, flow cytometry, and scratch and Boyden Chamber assays. For in vivo experiments, plakoglobin knockdown and control cells were inoculated into mammary fat pads of mice, and tumor growth, shedding of tumor cells into the bloodstream, and evidence of metastatic bone lesions were monitored with caliper measurement, flow cytometry, and microcomputed tomography (μCT), respectively. Plakoglobin and γ-catenin expression were reduced by more than 80% in all knockdown cell lines used but were unaltered after transfection with the scrambled sequence. Reduced plakoglobin resulted in significantly increased in MCF7 and T47D cell proliferation in vitro and in vivo, compared with control, with significantly more tumor cells being shed into the bloodstream of mice bearing plakoglobin knockdown tumors. In addition, plakoglobin knockdown cells showed a >250% increase in invasion through basement membrane and exhibited reduced cell-to-cell adhesion compared with control cells. Decreased plakoglobin expression increases the invasive behavior of breast cancer cells. This is the first demonstration of a functional role for plakoglobin/γ-catenin in the metastatic process, indicating that this molecule may represent a target for antimetastatic therapies.