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CIAPIN1基因沉默增强了体内耐药动物模型的化疗敏感性。

CIAPIN1 gene silencing enhances chemosensitivity in a drug-resistant animal model in vivo.

作者信息

Wang X M, Gao S J, Guo X F, Sun W J, Yan Z Q, Wang W X, Xu Y Q, Lu D

机构信息

Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.

Department of Breast Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.

出版信息

Braz J Med Biol Res. 2014 Apr;47(4):273-8. doi: 10.1590/1414-431x20133356. Epub 2014 Mar 21.


DOI:10.1590/1414-431x20133356
PMID:24676475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4075290/
Abstract

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.

摘要

细胞因子诱导的凋亡抑制因子1(CIAPIN1)的过表达导致乳腺癌的多药耐药(MDR)。本研究旨在评估通过RNA干扰(RNAi)沉默CIAPIN1基因作为耐药乳腺癌治疗方法的潜力,并研究CIAPIN1在体内对乳腺癌耐药性的影响。我们使用基于慢病毒载体的RNAi在携带MDR乳腺癌肿瘤的裸鼠中敲低CIAPIN1,发现慢病毒载体介导的CIAPIN1沉默在体内与化疗联合使用时能够有效且显著地抑制肿瘤生长。此外,蛋白质印迹分析表明,RNAi后CIAPIN1和P-糖蛋白的表达均有效下调,而P53上调。因此,我们得出结论,慢病毒载体介导的针对CIAPIN1的RNAi是逆转乳腺癌MDR的一种潜在方法。此外,CIAPIN1可能通过调节P-糖蛋白和P53的表达参与乳腺癌的MDR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/287ad09d6cb7/1414-431X-bjmbr-47-04-00273-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/b8ca4d709788/1414-431X-bjmbr-47-04-00273-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/a1892917cea2/1414-431X-bjmbr-47-04-00273-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/287ad09d6cb7/1414-431X-bjmbr-47-04-00273-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/b8ca4d709788/1414-431X-bjmbr-47-04-00273-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/a1892917cea2/1414-431X-bjmbr-47-04-00273-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc00/4075290/287ad09d6cb7/1414-431X-bjmbr-47-04-00273-gf003.jpg

相似文献

[1]
CIAPIN1 gene silencing enhances chemosensitivity in a drug-resistant animal model in vivo.

Braz J Med Biol Res. 2014-4

[2]
Down regulation of CIAPIN1 reverses multidrug resistance in human breast cancer cells by inhibiting MDR1.

Molecules. 2012-6-20

[3]
CIAPIN1 confers multidrug resistance by upregulating the expression of MDR-1 and MRP-1 in gastric cancer cells.

Cancer Biol Ther. 2006-3

[4]
CIAPIN1 confers multidrug resistance through up-regulation of MDR-1 and Bcl-L in LoVo/Adr cells and is independent of p53.

Oncol Rep. 2011-1-14

[5]
A new apoptosis inhibitor, CIAPIN1 (cytokine-induced apoptosis inhibitor 1), mediates multidrug resistance in leukemia cells by regulating MDR-1, Bcl-2, and Bax.

Biochem Cell Biol. 2007-12

[6]
Co-suppression of MDR1 (multidrug resistance 1) and GCS (glucosylceramide synthase) restores sensitivity to multidrug resistance breast cancer cells by RNA interference (RNAi).

Cancer Biol Ther. 2009-6

[7]
P-glycoprotein silencing with siRNA delivered by DOPE-modified PEI overcomes doxorubicin resistance in breast cancer cells.

Nanomedicine (Lond). 2012-1

[8]
Targeting ETS1 with RNAi-based supramolecular nanoassemblies for multidrug-resistant breast cancer therapy.

J Control Release. 2017-3-14

[9]
Reversal of MDR1/P-glycoprotein-mediated multidrug resistance by vector-based RNA interference in vitro and in vivo.

Cancer Biol Ther. 2006-1

[10]
[Reversal of multidrug resistance of gastric cancer cells by down-regulation of CIAPIN1 with CIAPIN1 siRNA].

Mol Biol (Mosk). 2008

引用本文的文献

[1]
The regulation of microRNAs on chemoresistance in triple-negative breast cancer: a recent update.

Epigenomics. 2024-4-19

[2]
Prediction of CIAPIN1 (Cytokine-Induced Apoptosis Inhibitor 1) Signaling Pathway and Its Role in Cholangiocarcinoma Metastasis.

J Clin Med. 2022-7-1

[3]
Hsa-miRNA-143-3p Reverses Multidrug Resistance of Triple-Negative Breast Cancer by Inhibiting the Expression of Its Target Protein Cytokine-Induced Apoptosis Inhibitor 1 .

J Breast Cancer. 2018-9

[4]
Upregulation of microRNA-143 reverses drug resistance in human breast cancer cells via inhibition of cytokine-induced apoptosis inhibitor 1.

Oncol Lett. 2017-6

本文引用的文献

[1]
Down regulation of CIAPIN1 reverses multidrug resistance in human breast cancer cells by inhibiting MDR1.

Molecules. 2012-6-20

[2]
Reversing multidrug resistance in breast cancer cells by silencing ABC transporter genes with nanoparticle-facilitated delivery of target siRNAs.

Int J Nanomedicine. 2012-6-5

[3]
Chemotherapy-resistant metastatic breast cancer.

Curr Treat Options Oncol. 2012-6

[4]
Trends in cancer mortality in China: an update.

Ann Oncol. 2012-4-6

[5]
p53 Family: Role of Protein Isoforms in Human Cancer.

J Nucleic Acids. 2012

[6]
Stable knockdown of MYCN by lentivirus-based RNAi inhibits human neuroblastoma cells growth in vitro and in vivo.

Biochem Biophys Res Commun. 2011-6-12

[7]
CIAPIN1 confers multidrug resistance through up-regulation of MDR-1 and Bcl-L in LoVo/Adr cells and is independent of p53.

Oncol Rep. 2011-1-14

[8]
Small interfering RNA for effective cancer therapies.

Mini Rev Med Chem. 2011-2

[9]
Viral vector-mediated RNA interference.

Curr Opin Pharmacol. 2010-7-9

[10]
CIAPIN1 as a therapeutic target in cancer.

Expert Opin Ther Targets. 2010-6

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