Association of BIM Deletion Polymorphism and BIM-γ RNA Expression in NSCLC with EGFR Mutation

This pilot study assessed the association of BIM deletion polymorphism and BIM RNA isoform in patients with EGFR-positive non-small cell lung cancer (NSCLC). The study included 33 patients with EGFR-positive NSCLC treated with gefitinib. BIM deletion polymorphism and BIM RNA isoform (EL/L/S/γ) were...

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Veröffentlicht in:Cancer Genomics & Proteomics 2016-11, Vol.13 (6), p.475-482
Hauptverfasser: Isobe, Kazutoshi, Kakimoto, Atsushi, Mikami, Tetsuo, Kaburaki, Kyohei, Kobayashi, Hiroshi, Yoshizawa, Takahiro, Makino, Takashi, Otsuka, Hajime, Sano, G O, Sugino, Keishi, Sakamoto, Susumu, Takai, Yujiro, Tochigi, Naobumi, Iyoda, Akira, Homma, Sakae
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Sprache:eng
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Zusammenfassung:This pilot study assessed the association of BIM deletion polymorphism and BIM RNA isoform in patients with EGFR-positive non-small cell lung cancer (NSCLC). The study included 33 patients with EGFR-positive NSCLC treated with gefitinib. BIM deletion polymorphism and BIM RNA isoform (EL/L/S/γ) were determined by polymerase chain reaction (PCR). BIM-γ expression was significantly higher in patients with BIM deletion polymorphism than among those without BIM deletion polymorphism inside tumors (p=0.038) and around tumors (p=0.0024). Relative BIM-γ expression was significantly higher in patients with BIM deletion polymorphism than among those without BIM deletion polymorphism (p=0.0017). Patients with BIM-γ had significantly shorter progression-free survival than those without BIM-γ (median: 304 vs. 732 days; p=0.023). Expression of BIM-γ mRNA and BIM deletion polymorphism were strongly associated. BIM-γ overexpression may have a role in apoptosis related to EGFR-tyrosine kinase inhibitor.
ISSN:1790-6245
1109-6535
1790-6245
DOI:10.21873/cgp.20010