KIT (CD117): a review on expression in normal and neoplastic tissues, and mutations and their clinicopathologic correlation

M Miettinen, J Lasota - Applied immunohistochemistry & molecular …, 2005 - journals.lww.com
CD117 (KIT) is a type III receptor tyrosine kinase operating in cell signal transduction in
several cell types. Normally KIT is activated (phosphorylated) by binding of its ligand, the …

[HTML][HTML] Receptor tyrosine kinases: Characterisation, mechanism of action and therapeutic interests for bone cancers

AI Ségaliny, M Tellez-Gabriel, MF Heymann… - Journal of bone …, 2015 - Elsevier
Bone cancers are characterised by the development of tumour cells in bone sites,
associated with a dysregulation of their environment. In the last two decades, numerous …

Morphologic and immunophenotypic diversity in Ewing family tumors: a study of 66 genetically confirmed cases

AL Folpe, JR Goldblum, BP Rubin… - The American journal …, 2005 - journals.lww.com
More than 85% of Ewing sarcoma/primitive neuroectodermal tumor (ES/PNET), or “Ewing
family of tumors”(EFTs), have the translocation, t (11; 22)(q24; q12), with others having …

A phase II study of imatinib mesylate in children with refractory or relapsed solid tumors: a Children's Oncology Group study

M Bond, ML Bernstein, A Pappo… - Pediatric blood & …, 2008 - Wiley Online Library
Background Imatinib mesylate is a small molecule inhibitor of certain tyrosine kinases, most
notably the chimeric bcr‐abl fusion protein found in CML. It also inhibits KIT and PDGF …

Synergistic antitumor effect of melatonin with several chemotherapeutic drugs on human Ewing sarcoma cancer cells: potentiation of the extrinsic apoptotic pathway

S Casado‐Zapico, J Rodriguez‐Blanco… - Journal of pineal …, 2010 - Wiley Online Library
Ewing sarcoma, the second most frequent bone cancer type, affects mainly adolescents,
who have a survival of 50% 5 yr after diagnosis. Current treatments include a combination of …

Targets for cancer therapy in childhood sarcomas

M Wachtel, BW Schäfer - Cancer treatment reviews, 2010 - Elsevier
Development of chemotherapeutic treatment modalities resulted in a dramatic increase in
the survival of children with many types of cancer. Still, in case of some pediatric cancer …

Insulin-like growth factor I receptor pathway inhibition by ADW742, alone or in combination with imatinib, doxorubicin, or vincristine, is a novel therapeutic approach in …

AS Martins, C Mackintosh, DH Martín, M Campos… - Clinical Cancer …, 2006 - AACR
Purpose: Ewing tumor cell survival and proliferation depends on several autocrine loops.
Targeting these loops is a promising therapeutic approach. We recently showed the …

Inducible expression of chimeric EWS/ETS proteins confers Ewing's family tumor-like phenotypes to human mesenchymal progenitor cells

Y Miyagawa, H Okita, H Nakaijima… - … and cellular biology, 2008 - Am Soc Microbiol
Ewing's family tumor (EFT) is a rare pediatric tumor of unclear origin that occurs in bone and
soft tissue. Specific chromosomal translocations found in EFT cause EWS to fuse to a subset …

The stem cell factor/c-kit receptor pathway enhances proliferation and invasion of pancreatic cancer cells

A Yasuda, H Sawai, H Takahashi, N Ochi, Y Matsuo… - Molecular cancer, 2006 - Springer
Background The transmembrane protein c-kit is a receptor tyrosine kinase (KIT) and KIT is
expressed in solid tumors and hematological malignancies such as gastrointestinal stromal …

Blocking the road, stopping the engine or killing the driver? Advances in targeting EWS/FLI-1 fusion in Ewing sarcoma as novel therapy

H Kovar - Expert opinion on therapeutic targets, 2014 - Taylor & Francis
Introduction: Ewing sarcoma (ES) represents the paradigm of an aberrant E-twenty-six (ETS)
oncogene-driven cancer. It is characterized by specific rearrangements of one of five …