Comment[ArrayExpressAccession] E-GEOD-43097 MAGE-TAB Version 1.1 Public Release Date 2014-05-02 Investigation Title Integrin α3b1-dependent gene expression in MDA-MB-231 breast cancer cells Comment[Submitted Name] Integrin α3b1-dependent gene expression in MDA-MB-231 breast cancer cells Experiment Description Gene-level and exon-level analysis of gene expression in MDA-MB-231 cells that stably express control shRNA or integrin α3-targeting shRNA. The laminin-332-binding integrin α3b1 is expressed highly in many breast cancer cells, but its roles in regulating gene expression programs that promote breast cancer progression have not been explored. In order to identify genes that are regulated by α3b1 in human breast cancer cells, we used a lentiviral approach to express an α3-targeting shRNA to suppress integrin α3b1 in MDA-MB-231 cells, and we identified subsequent changes in gene expression and alternate exon useage. We used the Affymetrix Human Exon 1.0 ST platform to analyze biological replicates of MDA-MB-231 cells that were transduced with lentivirus to stably express either control shRNA or α3-targeting shRNA. Array data was processed by Affymetrix Exon Array Computational Tool. Term Source Name ArrayExpress EFO Term Source File http://www.ebi.ac.uk/arrayexpress/ http://www.ebi.ac.uk/efo/efo.owl Person Last Name Chittur DiPersio Subbaram Chittur Person First Name Sridar C Sita Sridar Person Mid Initials M V Person Email schittur@albany.edu Person Affiliation SUNY-University at Albany Person Phone 518-591-7215 Person Address Center for Functional Genomics, SUNY-University at Albany, One Discovery Drive, CRC 342G, Rensselaer, NY, USA Person Roles submitter Protocol Name P-GSE43097-1 P-GSE43097-4 P-GSE43097-5 P-GSE43097-2 P-GSE43097-3 P-GSE43097-6 Protocol Description CHP files generated at both gene- and exon-level with Affymetrix Expression Console using Core probeset ID_REF = VALUE = Quantification Standard Affymetrix WT protocol starting with 1ug total RNA and incuding riboreduction Standard Affymetrix WT protocol MDA-MB-231 cells with stable expression of either control shRNA or α3-targeting shRNA were maintained at 37 degrees C, 5% CO2, on standard tissue culture plates. Cells were grown in DMEM supplemented with 10% FBS 100 units/ml penicillin and 100 μg/ml streptomycin. Total cellular RNA was isolated from cells using the RNeasy Plus isolation kit (Qiagen, Valencia, CA), and quality was confirmed on an Agilent Bioanalyzer. Standard Affymetrix rotocol for GCS30007G scanner Protocol Type normalization data transformation protocol labelling protocol hybridization protocol growth protocol nucleic acid extraction protocol array scanning protocol Experimental Factor Name GENOTYPE Experimental Factor Type genotype PubMed ID 24434582 Comment[SecondaryAccession] GSE43097 Comment[GEOReleaseDate] 2014-05-02 Comment[ArrayExpressSubmissionDate] 2012-12-21 Comment[GEOLastUpdateDate] 2014-05-02 Comment[AEExperimentType] transcription profiling by array Comment[AdditionalFile:Data1] GSE43097_MD_1_MBA231_con1.CEL Comment[AdditionalFile:Data2] GSE43097_MD_2_MBA231_con2.CEL Comment[AdditionalFile:Data3] GSE43097_MD_3_MBA231_alpha3_kd1.CEL Comment[AdditionalFile:Data4] GSE43097_MD_4_MBA231_alpha3_kd2.CEL SDRF File E-GEOD-43097.sdrf.txt