In vitro modulation of Bcl-2 levels in small cell lung cancer cells: effects on cell viability

Brazilian Journal of Medical and Biological Research

A.o. Santos²  J.p. Pereira²  M.c. Pedroso De Lima¹  S. Simões²  J.n. Moreira² 

[1] ,University of Coimbra Faculty of Pharmacy Laboratory of Pharmaceutical Technology

关键词: Small cell lung cancer;    Gene silencing;    Bcl-2;    siRNA;    Antisense ODN;    Flow cytometry;    Chemosensitization;   

DOI  :  10.1590/S0100-879X2010007500099

来源: SciELO

【 摘 要 】

Small cell lung cancer (SCLC) is an aggressive disease, representing 15% of all cases of lung cancer, has high metastatic potential and low prognosis that urgently demands the development of novel therapeutic approaches. One of the proposed approaches has been the down-regulation of BCL2, with poorly clarified and controversial therapeutic value regarding SCLC. The use of anti-BCL2 small interfering RNA (siRNA) in SCLC has never been reported. The aim of the present study was to select and test the in vitro efficacy of anti-BCL2 siRNA sequences against the protein and mRNA levels of SCLC cells, and their effects on cytotoxicity and chemosensitization. Two anti-BCL2 siRNAs and the anti-BCL2 G3139 oligodeoxynucleotide (ODN) were evaluated in SCLC cells by the simultaneous determination of Bcl-2 and viability using a flow cytometry method recently developed by us in addition to Western blot, real-time reverse-transcription PCR, and cell growth after single and combined treatment with cisplatin. In contrast to previous reports about the use of ODN, a heterogeneous and up to 80% sequence-specific Bcl-2 protein knockdown was observed in the SW2, H2171 and H69 SCLC cell lines, although without significant sequence-specific reduction of cell viability, cell growth, or sensitization to cisplatin. Our results question previous data generated with antisense ODN and supporting the present concept of the therapeutic interest in BCL2 silencing per se in SCLC, and support the growing notion of the necessity of a multitargeting molecular approach for the treatment of cancer.

【 授权许可】

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