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181   $ctxt$2rdacontent
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200 10$aScaffold Protein p140Cap as a Molecular Hub for Limiting Cancer Progression $eA New Paradigm in Neuroblastoma /$fwritten by Giorgia Centonze [and eight others]
210  1$aLondon :$cIntechOpen,$d2021.
215   $a1 online resource (130 pages)
311   $a1-83969-050-X 
327   $a1. Introduction -- 2. The p140Cap adaptor protein -- 3. SRCIN1 mRNA expression is an independent prognostic marker for NB -- 4. p140Cap negatively affects tumorigenic features -- 5. Molecular mechanisms and therapeutic targets in neuroblastoma -- 6. p140Cap impairs the Src/p130Cas and the STAT3/Jak2 signaling pathways -- 7. p140Cap increases NB cell sensitivity to chemotherapeutic treatment -- 8. p140Cap increases NB cell sensitivity to Src kinase inhibitors -- 9. Conclusions -- Acknowledgments -- Conflict of interest -- Rights and permissions -- Abbreviations -- References.
330   $aNeuroblastoma, the most common extra-cranial pediatric solid tumor, is responsible for 9-15% of all pediatric cancer deaths. Its intrinsic heterogeneity makes it difficult to successfully treat, resulting in overall survival of 50% for half of the patients. Here we analyze the role in neuroblastoma of the adaptor protein p140Cap, encoded by the SRCIN1 gene. RNA-Seq profiles of a large cohort of neuroblastoma patients show that SRCIN1 mRNA levels are an independent risk factor inversely correlated to disease aggressiveness. In high-risk patients, SRCIN1 was frequently altered by hemizygous deletion, copy-neutral loss of heterozygosity, or disruption. Functional assays demonstrated that p140Cap is causal in dampening both Src and Jak2 kinase activation and STAT3 phosphorylation. Moreover, p140Cap expression decreases in vitro migration and anchorage-independent cell growth, and impairs in vivo tumor progression, in terms of tumor volume and number of spontaneous lung metastasis. p140Cap also contributes to an increased sensitivity of neuroblastoma cells to chemotherapy drugs and to the combined usage of doxorubicin and etoposide with Src inhibitors. Overall, we provide the first evidence that SRCIN1/p140Cap is a new independent prognostic marker for patient outcome and treatment, with a causal role in curbing the aggressiveness of neuroblastoma. We highlight the potential clinical impact of SRCIN1/p140Cap expression in neuroblastoma tumors, in terms of reducing cytotoxic effects of chemotherapy, one of the main issues for pediatric tumor treatment.
517   $aScaffold Protein p140Cap as a Molecular Hub for Limiting Cancer Progression
606   $aNeuroblastoma
615  0$aNeuroblastoma.
676   $a616.9948
700   $aCentonze$b Giorgia$01348392
801  0$bNjHacI
801  1$bNjHacl
906   $aBOOK
912   $a9910633982803321
996   $aScaffold Protein p140Cap as a Molecular Hub for Limiting Cancer Progression$93085871
997   $aUNINA