<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/003/SRR2973263/SRR2973263_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/002/SRR2973262/SRR2973262_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/000/SRR2973260/SRR2973260_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/009/SRR2973259/SRR2973259_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/002/SRR2973262/SRR2973262_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/009/SRR2973259/SRR2973259_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/003/SRR2973263/SRR2973263_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/001/SRR2973261/SRR2973261_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/003/SRR2973213/SRR2973213_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/000/SRR2973260/SRR2973260_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/001/SRR2973261/SRR2973261_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR297/003/SRR2973213/SRR2973213_2.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Vanderbilt University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA304768</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>It is increasingly appreciated that properties of cultured epithelial cells differ dramatically in 2D compared to 3D, and the latter more faithfully recapitulates in vivo behavior. By studying a battery of human colorectal cancer (CRC) cell lines in type-1 collagen, we have found that HCA-7 cells form colonies with two distinctive and persistent morphological and functional properties. We observed predominantly single-layered polarized cysts (cystic colonies, CC) and a smaller fraction displaying disorganized solid masses (spiky colonies, SC) that were highly invasive in vivo. Despite overall genomic similarity, CC and SC exhibited distinct and dynamic patterns of gene expression in 3D that could largely be attributed to global changes in histone methylation. One of the most upregulated genes in CC was the prostaglandin-degrading enzyme HPGD that exhibits tumor-suppressive activity by metabolizing PGE2 to 15-keto-PGE2. HPGD protein and 15-keto-PGE2 were elevated in CC in 3D as was HPGD protein in nude mouse xenografts. The most upregulated gene in SC was versican (VCAN) and VCAN protein was markedly increased in SC conditioned medium and in SC nude mouse xenografts. Comparative ChIP analysis between CC and SC in 3D revealed extensive reprogramming of chromatin modifications across the VCAN locus in the absence of copy number changes, suggesting an epigenetic basis for overexpression of VCAN in SC cells. Analysis of a CRC tissue microarray revealed that epithelial, but not stromal, VCAN staining correlated with reduced survival, and combined epithelial VCAN and absent HPGD staining portended a poorer prognosis. We demonstrate the utility of this 3D system to identify disease-relevant genes in CRC.</long_description><repository>ENA</repository><description_synonyms>other disease, Colorectal Neoplasm, Carcinoma, Materials, Colorectal Cancer, Neoplasms, disorders, Gene, medical condition, Cultural Backgrounds, Tumor, Cistrons, autosomal dominant, Colorectal, colorectal cancer, Background, Cultural Background, Cultures, diseases, Cultural, Diseases, Neoplasm, disease or disorder, condition, Genetic Materials, diseases and disorders, CRC, Colorectal Cancers, Genetic Material, Backgrounds, Colorectal Tumors, Carcinomas, large bowel cancer, ethnicity, human disease, anatomical systems, Genetic, Cultural Beliefs, susceptibility to, Colorectal Carcinoma, Cultural Relativisms, Colorectal Carcinomas, Cancers, Colorectal Tumor, cancer of large bowel, large intestine cancer, non-neoplastic, cancer of the large intestine, disease, colon cancer, Material, Customs, cancer of the large bowel, Relativisms, disorder, Homo sapiens disease, Cistron, culture, cancer of large intestine, colorectal (colon or rectal) cancer., Relativism, Cultural Relativism, somatic mutation, Tumors, Cancer</description_synonyms><name_synonyms>Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern Man</name_synonyms></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>A new 3D culture system to identify disease-relevant genes in colorectal cancer</description><dates><last_updated>2025-09-24</last_updated><first_public>2017-04-19</first_public></dates><accession>PRJNA304768</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>