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Knockdown of OCT4 may sensitize NSCLC cells to cisplatin
Liu, X; Ma, M; Duan, X; Zhang, H; Yang, M.
Afiliação
  • Liu, X; Tianjin Medical University Cancer Institute and Hospital. The Second Department of Thoracic Oncology. Key Laboratory of Cancer Prevention and Therapy. Tianjin. China
  • Ma, M; Tianjin Medical University Cancer Institute and Hospital. The Second Department of Thoracic Oncology. Key Laboratory of Cancer Prevention and Therapy. Tianjin. China
  • Duan, X; Tianjin Medical University Cancer Institute and Hospital. The Second Department of Thoracic Oncology. Key Laboratory of Cancer Prevention and Therapy. Tianjin. China
  • Zhang, H; Tianjin Medical University Cancer Institute and Hospital. The Second Department of Thoracic Oncology. Key Laboratory of Cancer Prevention and Therapy. Tianjin. China
  • Yang, M; Tianjin Medical University Cancer Institute and Hospital. The Second Department of Thoracic Oncology. Key Laboratory of Cancer Prevention and Therapy. Tianjin. China
Clin. transl. oncol. (Print) ; 19(5): 587-592, mayo 2017. ilus, graf
Artigo em Inglês | IBECS | ID: ibc-162192
Biblioteca responsável: ES1.1
Localização: BNCS
ABSTRACT
Purpose. Cisplatin is commonly used in non-small-cell lung cancer (NSCLC) chemotherapy; however, chemoresistance to cisplatin remains a great clinical challenge. Octamer-binding protein 4 (OCT4) has been reported to be overexpressed in NSCLC. In this study, we aimed to investigate the potential role of OCT4 in NSCLC with chemoresistance to cisplatin. Methods. Expressions of OCT4 was detected in NSCLC tissues and cell lines. We utilized siRNA to knock down OCT4 expression in human NSCLC cells and analyzed their phenotypic changes. Results. We found that the difference of OCT4 expression between NSCLC and the adjacent non-tumourous tissues was statistically significant. Knockdown of OCT4 in NSCLC cells could decrease cell proliferation, and potentiate apoptosis induced by cisplatin, suggesting OCT4 may contribute to cisplatin resistance in NSCLC. Conclusion. Our findings indicate that targeting OCT4 could improve cisplatin effect in NSCLC, confirming their role in modulating cisplatin sensitivity (AU)
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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Cisplatino / Carcinoma Pulmonar de Células não Pequenas / Fatores de Transcrição de Octâmero Limite: Feminino / Humanos / Masculino Idioma: Inglês Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Artigo Instituição/País de afiliação: Tianjin Medical University Cancer Institute and Hospital/China
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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Cisplatino / Carcinoma Pulmonar de Células não Pequenas / Fatores de Transcrição de Octâmero Limite: Feminino / Humanos / Masculino Idioma: Inglês Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Artigo Instituição/País de afiliação: Tianjin Medical University Cancer Institute and Hospital/China
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