Are two better than one? A novel double‐mutant KIT in GIST that responds to Imatinib. Issue 4 (21st March 2013)

• Record Type: Journal Article
• Authors: Conca, Elena; Miranda, Claudia; Col, Valentina Dal; Fumagalli, Elena; Pelosi, Giuseppe; Mazzoni, Mara; Fermeglia, Maurizio; Laurini, Erik; Pierotti, Marco A.; Pilotti, Silvana; Greco, Angela; Pricl, Sabrina; Tamborini, Elena
• Is Part Of: Molecular oncology. Volume 7:Issue 4(2013:Aug.)
• Page Start: 756
• Page End: 762
• Publication Date: 2013-03-21
• Subjects: GIST -- Imatinib -- KIT mutations -- Molecular modeling -- Free energy of binding -- Functional analysis; Cancer -- Molecular aspects -- Periodicals; 616.994005
• DOI: 10.1016/j.molonc.2013.02.019
• Languages: English
• ISSNs: 1574-7891

Abstract

Abstract : Gastrointestinal stromal tumors carry in about 85% of the cases activating mutations in KIT gene. Generally only one KIT mutation is found in primary tumors and the majority of mutations affecting KIT exon 11 is sensitive to Imatinib. We report upon a GIST case harboring a double‐mutant KIT gene at exon 11, which expresses a receptor bearing the known activating W557G mutation and a newly discovered missense Y578C alteration. The relative affinities for ATP and Imatinib of each single (W557G, Y578C) and double (W557G/Y578C) mutant KITs were predicted by in silico studies (computer‐based molecular simulations), and compared with those obtained for known Imatinib sensitive and resistant KIT mutants. In parallel, biochemical analysis of the single and double KIT mutants expressed in mammalian cells was performed. Both the in‐silico/in‐vitro investigations showed constitutive activation and sensitivity to Imatinib of the yet mentioned Y578C mutation as well as of the double mutant, providing evidence that the concomitant presence of the W557G and Y578C mutations does not affect Imatinib response compare to the single mutations, in line with what observed in Imatinib treated patient. Highlights: ► Two mutations, one novel, in KIT exon 11 were identified in one GIST patient. ► KIT exon 11 PCR fragment subcloning showed the mutations were on the same allele. ► KIT receptor carries the two corresponding aminoacidic substitutions. ► Biochemical/ in silico analyses showed double KIT mutant is Imatinib sensitive. ► The patient, Imatinib treated, continues to respond well to the therapy.