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Validating the effect of anti-angiogenic treatment on tumor cell invasion and metastasis in NSCLC

Subject Area Hematology, Oncology
Term from 2014 to 2017
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 256380049
 
Final Report Year 2018

Final Report Abstract

Anti-angiogenic treatment targeting VEGF-VEGFR2 signaling has shown limited efficacy in lung cancer patients. Here, we demonstrate that inhibition of VEGFR2 in tumor cells – which is expressed in around 20% of NSCLC patients – leads to a proinvasive phenotype. Druginduced inhibition of tumor VEGFR2 releases a newly identified EphA2/VEGFR2 heterocomplex, thereby allowing RSK to interact with Serine 897 of EphA2. Inhibition of RSK decreases phosphorylation of Serine 897 EphA2. Selective genetic modeling of Serine 897 of EphA2 or inhibition of EphA2 abrogates the formation of metastases in vivo upon VEGFR2 inhibition. In summary, these findings demonstrate that VEGFR2-targeted therapy conditions VEGFR2-positive NSCLC to Serine 897 EphA2-dependent aggressive tumor growth and metastasis. These data shed light on the molecular mechanisms explaining the limited efficacy of VEGFR2-targeted anti-angiogenic treatment in lung cancer patients.

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