<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Yeh CY</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>A cross-talk between different receptor tyrosine kinases (RTKs) plays an important role in the pathogenesis of human cancers.&lt;h4>Methods&lt;/h4>Both NIH-Met5 and T24-Met3 cell lines harboring an inducible human c-Met gene were established. C-Met-related RTKs were screened by RTK microarray analysis. The cross-talk of RTKs was demonstrated by Western blotting and confirmed by small interfering RNA (siRNA) silencing, followed by elucidation of the underlying mechanism. The impact of this cross-talk on biological function was demonstrated by Trans-well migration assay. Finally, the potential clinical importance was examined in a cohort of 65 cases of locally advanced and metastatic bladder cancer patients.&lt;h4>Results&lt;/h4>A positive association of Axl or platelet-derived growth</pubmed_abstract><journal>BMC cancer</journal><pagination>139</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3101176</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transcriptional activation of the Axl and PDGFR-α by c-Met through a ras- and Src-independent mechanism in human bladder cancer.</pubmed_title><pmcid>PMC3101176</pmcid><pubmed_authors>Chow NH</pubmed_authors><pubmed_authors>Yeh CY</pubmed_authors><pubmed_authors>Shin JW</pubmed_authors><pubmed_authors>Wu TJ</pubmed_authors><pubmed_authors>Lee CT</pubmed_authors><pubmed_authors>Chang TY</pubmed_authors><pubmed_authors>Lee YC</pubmed_authors><pubmed_authors>Raghavaraju G</pubmed_authors><pubmed_authors>Shin SM</pubmed_authors><pubmed_authors>Tseng VS</pubmed_authors><pubmed_authors>Shen CH</pubmed_authors><pubmed_authors>Yeh HH</pubmed_authors><pubmed_authors>Chiang JH</pubmed_authors><pubmed_authors>Liu HS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptional activation of the Axl and PDGFR-α by c-Met through a ras- and Src-independent mechanism in human bladder cancer.</name><description>&lt;h4>Background&lt;/h4>A cross-talk between different receptor tyrosine kinases (RTKs) plays an important role in the pathogenesis of human cancers.&lt;h4>Methods&lt;/h4>Both NIH-Met5 and T24-Met3 cell lines harboring an inducible human c-Met gene were established. C-Met-related RTKs were screened by RTK microarray analysis. The cross-talk of RTKs was demonstrated by Western blotting and confirmed by small interfering RNA (siRNA) silencing, followed by elucidation of the underlying mechanism. The impact of this cross-talk on biological function was demonstrated by Trans-well migration assay. Finally, the potential clinical importance was examined in a cohort of 65 cases of locally advanced and metastatic bladder cancer patients.&lt;h4>Results&lt;/h4>A positive association of Axl or platelet-derived growth</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Apr</publication><modification>2026-04-07T14:00:22.153Z</modification><creation>2026-04-07T13:42:40.43Z</creation></dates><accession>S-EPMC3101176</accession><cross_references><pubmed>21496277</pubmed><doi>10.1186/1471-2407-11-139</doi></cross_references></HashMap>