{"owner": "ArrayExpress Uploader", "pop_total": 0, "species": "human", "factors": [{"GSM914190": {"CELL LINE": "LNCAP", "CELL TYPE": "Human prostate cancer"}}, {"GSM914190": {"CELL LINE": "LNCAP", "CELL TYPE": "Human prostate cancer"}}, {"GSM914188": {"CELL LINE": "HBC5", "CELL TYPE": "Human breast cancer"}}, {"GSM914188": {"CELL LINE": "HBC5", "CELL TYPE": "Human breast cancer"}}], "id": 2069, "ownerprofile_id": "arrayexpress_sid", "platform": 4, "summary_wrapped": "De novo lipogenesis is activated in most cancers. Several lipogenic enzymes are implicated in oncogenesis and represent potential cancer...", "geo_gse_id": "E-GEOD-37243", "owner_profile": "/profile/8773/arrayexpressuploader", "factor_count": 2, "sample_count": 4, "tags": ["basal", "cancer", "cell", "colon", "colon cancer", "fatty acid", "line", "lipid", "protein"], "lastmodified": "Dec.12, 2014", "is_default": false, "geo_gds_id": "", "slug": "expression-data-by-acly-knockdown", "geo_id_plat": "E-GEOD-37243_A-AFFY-44", "name": "Expression data by ACLY knockdown", "created": "Jul.11, 2014", "summary": "De novo lipogenesis is activated in most cancers. Several lipogenic enzymes are implicated in oncogenesis and represent potential cancer therapeutic targets. RNA interference-mediated depletion of ATP citrate lyase (ACLY), the enzyme that catalyzes the first step of de novo lipogenesis, leads to growth suppression in a subset of human cancer cells. Here we demonstrate the molecular basis and potential biomarkers for ACLY-targeting therapy. First, suppression of cancer cell growth by ACLY depletion involves down-regulation of fatty acid elongase ELOVL6 at the transcriptional level. Lipid profiling revealed that ACLY depletion alters fatty acid composition in triglyceride; increased palmitate and decreased longer fatty acids, in accordance with ELOVL6 down-regulation. Second, ACLY depletion increases reactive oxygen species (ROS), whereas addition of antioxidant reduces ROS and attenuates the growth suppression. Third, ACLY depletion or ROS stimulation induce phosphorylation of AMP-activated protein kinase (AMPK), a sensor of energy and lipid metabolism. Analysis of various cancer cell lines revealed that the levels of AMPK phosphorylation (p-AMPK) correlate with the basal ROS levels, and that cancer cells with low basal p-AMPK (i.e., low basal ROS) levels are highly susceptible to ACLY depletion-mediated growth suppression. Finally, in clinical colon cancer tissues, p-AMPK levels are significantly decreased in aggressive tumors and correlate with the levels of 8-hydroxydeoxyguanosine, a hallmark of ROS stimulation. Together, these data suggest that ACLY inhibition suppresses cancer growth via palmitate-mediated lipotoxicity, and p-AMPK could be a predictive biomarker for its therapeutic outcome. Two cell lines are treated with ACLY siRNA. The samples include controls of each cell line.", "source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-37243", "sample_source": "http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-37243/samples/"}