Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of human xenograft laboratory models and primary tumors of small cell lung cancer


ABSTRACT: Gene expression was measured on the Affymetrix platform in primary xenografts, xenograft-derived cell lines, secondary xenografts, normal lung, and primary tumors obtained from chemotherapy naive Small Cell Lung Cancer (SCLC). The SCLC primary xenografts were serially propagated in vivo in immunodeficient mice. Cell lines were derived from each xenograft and grown for 6 months using conventional tissue culture conditions. Secondary xenografts were obtained from cell cultures by re-implantation in immunodeficient mice. Such SCLC laboratory models were analyzed along with conventional SCLC cell lines and the derivative secondary xenografts, with normal lung and primary tumors, to assess irreversible gene expression changes induced by culturing conditions. Experiment Overall Design: SCLC primary xenografts were compared to the corresponding xenograft-derived cell lines, and to the secondary xenografts established from the cell lines using the Affymetrix GeneChip Human Genome U133 Plus 2.0 Array. Gene expression from SCLC primary tumors was measured using the Affymetrix GeneChip Human Genome U133A 2.0 Array. 3 datasets: GSM380476-GSM380512, GSM380513-GSM380516, and GSM380517-GSM380520

ORGANISM(S): Homo sapiens

SUBMITTER: Luigi Marchionni 

PROVIDER: E-GEOD-15240 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

A primary xenograft model of small-cell lung cancer reveals irreversible changes in gene expression imposed by culture in vitro.

Daniel Vincent C VC   Marchionni Luigi L   Hierman Jared S JS   Rhodes Jonathan T JT   Devereux Wendy L WL   Rudin Charles M CM   Yung Rex R   Parmigiani Giovanni G   Dorsch Marion M   Peacock Craig D CD   Watkins D Neil DN  

Cancer research 20090407 8


Traditional approaches to the preclinical investigation of cancer therapies rely on the use of established cell lines maintained in serum-based growth media. This is particularly true of small-cell lung cancer (SCLC), where surgically resected tissue is rarely available. Recent attention has focused on the need for better models that preserve the integrity of cancer stem cell populations, as well as three-dimensional tumor-stromal interactions. Here we describe a primary xenograft model of SCLC  ...[more]

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