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CIAPIN1 gene silencing enhances chemosensitivity in a drug-resistant animal model in vivo.
Wang, X M; Gao, S J; Guo, X F; Sun, W J; Yan, Z Q; Wang, W X; Xu, Y Q; Lu, D.
Affiliation
  • Wang XM; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Gao SJ; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Guo XF; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Sun WJ; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Yan ZQ; Department of Breast Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Wang WX; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Xu YQ; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
  • Lu D; Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
Braz J Med Biol Res ; 47(4): 273-8, 2014 Apr.
Article in En | MEDLINE | ID: mdl-24676475
Overexpression of cytokine-induced apoptosis inhibitor 1 (CIAPIN1) contributes to multidrug resistance (MDR) in breast cancer. This study aimed to evaluate the potential of CIAPIN1 gene silencing by RNA interference (RNAi) as a treatment for drug-resistant breast cancer and to investigate the effect of CIAPIN1 on the drug resistance of breast cancer in vivo. We used lentivirus-vector-based RNAi to knock down CIAPIN1 in nude mice bearing MDR breast cancer tumors and found that lentivirus-vector-mediated silencing of CIAPIN1 could efficiently and significantly inhibit tumor growth when combined with chemotherapy in vivo. Furthermore, Western blot analysis showed that both CIAPIN1 and P-glycoprotein expression were efficiently downregulated, and P53 was upregulated, after RNAi. Therefore, we concluded that lentivirus-vector-mediated RNAi targeting of CIAPIN1 is a potential approach to reverse MDR of breast cancer. In addition, CIAPIN1 may participate in MDR of breast cancer by regulating P-glycoprotein and P53 expression.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Doxorubicin / Drug Resistance, Neoplasm / Gene Silencing / Intracellular Signaling Peptides and Proteins / Antibiotics, Antineoplastic Limits: Animals / Female / Humans Language: En Journal: Braz J Med Biol Res Year: 2014 Document type: Article Affiliation country: China Country of publication: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Doxorubicin / Drug Resistance, Neoplasm / Gene Silencing / Intracellular Signaling Peptides and Proteins / Antibiotics, Antineoplastic Limits: Animals / Female / Humans Language: En Journal: Braz J Med Biol Res Year: 2014 Document type: Article Affiliation country: China Country of publication: Brazil