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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="id">8233</item><item key="factors"><item><item key="GSM361017"><item key="SAMPLE">SZ32</item><item key="SEX">M</item></item></item><item><item key="GSM361018"><item key="SAMPLE">SZ20</item><item key="SEX">M</item></item></item><item><item key="GSM361019"><item key="SAMPLE">SZ26</item><item key="SEX">M</item></item></item><item><item key="GSM361020"><item key="SAMPLE">SZ33</item><item key="SEX">M</item></item></item><item><item key="GSM36102"><item key="SAMPLE">SZ27</item><item key="SEX">M</item></item></item><item><item key="GSM361022"><item key="SAMPLE">SZ19</item><item key="SEX">M</item></item></item><item><item key="GSM361023"><item key="SAMPLE">SZ21</item><item key="SEX">M</item></item></item><item><item key="GSM361024"><item key="SAMPLE">SZ23</item><item key="SEX">M</item></item></item><item><item key="GSM361025"><item key="SAMPLE">SZ25</item><item key="SEX">M</item></item></item><item><item key="GSM361026"><item key="SAMPLE">SZ14</item><item key="SEX">M</item></item></item><item><item key="GSM361027"><item key="SAMPLE">SZ15</item><item key="SEX">F</item></item></item><item><item key="GSM361028"><item key="SAMPLE">SZ17</item><item key="SEX">M</item></item></item><item><item key="GSM361029"><item key="SAMPLE">SZ22</item><item key="SEX">M</item></item></item><item><item key="GSM361030"><item key="SAMPLE">SZ31</item><item key="SEX">M</item></item></item><item><item key="GSM36103"><item key="SAMPLE">SZ18</item><item key="SEX">M</item></item></item><item><item key="GSM361032"><item key="SAMPLE">SZ24</item><item key="SEX">M</item></item></item></item><item key="pop_total">0</item><item key="platform">7</item><item key="summary_wrapped">The biologic basis for NSCLC metastasis is not well understood. Here we addressed this deficiency by transcriptionally profiling tumors...</item><item key="pubmed_id">19404390</item><item key="geo_gse_id">E-GEOD-14449</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">16</item><item key="tags"><item>adenocarcinoma</item><item>disease</item><item>liquid</item><item>lung</item><item>lung adenocarcinoma</item><item>nsclc</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-14449_A-AFFY-23</item><item key="slug">gene-expression-profiles-of-spontaneous-metastasis</item><item key="geo_gds_id"/><item key="name">Gene expression profiles of spontaneous metastasis in a K-ras/p53 mutant mouse model</item><item key="created">Nov.23, 2014</item><item key="summary">The biologic basis for NSCLC metastasis is not well understood. Here we addressed this deficiency by transcriptionally profiling tumors from a genetic mouse model of human lung adenocarcinoma that develops metastatic disease owing to the expression of K-rasG12D and p53R172H. We identified 2,209 genes that were differentially expressed in distant metastases relative to matched lung tumors. Mining of publicly available data bases revealed this expression signature in a subset of NSCLC patients who had a poorer prognosis than those without the signature. Primary lung adenocarcinomas and metastases from p53R172H&#8710;g/+ K-rasLA1/+ mice or syngeneic tumors were isolated, carefully dissected to remove the adjacent tissue, snap-frozen in liquid nitrogen and stored at -80&#176; until use. Part of each dissected tumor was histologically evaluated by a board-certified pathologist.  Synthesis of cRNA and hybridization to Mouse Expression Array 430A 2.0 chips were performed.  Two-sided t-paired tests using log-transformed expression values determined significant differences between primary tumors and metastasis.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-14449</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-14449/samples/</item></data></biogps>
