Literature DB >> 27807070

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

Kazutoshi Isobe1, Atsushi Kakimoto2, Tetsuo Mikami3, Kyohei Kaburaki2, Hiroshi Kobayashi2, Takahiro Yoshizawa2, Takashi Makino4, Hajime Otsuka4, G O Sano2, Keishi Sugino2, Susumu Sakamoto2, Yujiro Takai2, Naobumi Tochigi5, Akira Iyoda3, Sakae Homma2.   

Abstract

AIM: 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). PATIENTS AND METHODS: 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).
RESULTS: 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).
CONCLUSION: 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. Copyright
© 2016, International Institute of Anticancer Research (Dr. John G. Delinasios), All rights reserved.

Entities:  

Keywords:  BIM; epidermal growth factor receptor tyrosine kinase inhibitor; non-small cell lung cancer

Mesh:

Substances:

Year:  2016        PMID: 27807070      PMCID: PMC5219921          DOI: 10.21873/cgp.20010

Source DB:  PubMed          Journal:  Cancer Genomics Proteomics        ISSN: 1109-6535            Impact factor:   4.069


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