Onconase mediated NFKβ downregulation in malignant pleural mesothelioma

被引:51
|
作者
Goparaju, C. M. [1 ]
Blasberg, J. D. [2 ]
Volinia, S. [3 ]
Palatini, J. [3 ]
Ivanov, S. [4 ]
Donington, J. S. [1 ]
Croce, C. [3 ]
Carbone, M. [5 ]
Yang, H. [5 ]
Pass, H. I. [1 ]
机构
[1] NYU, Med Ctr, Dept Cardiothorac Surg, New York, NY 10016 USA
[2] Columbia Univ Coll Phys & Surg, St Lukes Roosevelt Med Ctr, Dept Gen Surg, New York, NY 10032 USA
[3] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[4] Vanderbilt Univ, Med Ctr, Dept Otolaryngol, Nasville, TN USA
[5] Univ Hawaii, Canc Res Ctr Hawaii, Honolulu, HI 96813 USA
关键词
mesothelioma; microRNA; multidrug resistance; CYTOTOXIC RIBONUCLEASE ONCONASE; TYROSINE KINASE INHIBITOR; HUMAN LUNG-CANCER; KAPPA-B; ANTITUMOR RIBONUCLEASE; CELL-LINES; EXPRESSION PROFILES; RADIATION RESPONSE; INDUCED APOPTOSIS; DRUG-RESISTANCE;
D O I
10.1038/onc.2010.643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Treatment of malignant pleural mesothelioma (MPM) with Ranpirnase (Onconase) results in disruption of protein translation and cell apoptosis. We hypothesize that Onconase exerts an effect via downregulation of nuclear factor kappa B (NFK beta) by specific microRNAs (miRNAs) and that interference of this pathway could have implications for MPM resistance to chemotherapy. Three immortalized MPM cell lines (H2959, H2373 and H2591) were exposed to Onconase at 0-20 mu g/ml. Cell counts were measured at 48 and 72 h. Gene expression in miRNA-enriched RNA was validated by reverse transcription-PCR (RT-PCR). The functional implications of miRNA expression were evaluated by transfecting miRNA mimics or inhibitors into MPM cell lines, and performing Matrigel invasion, cell proliferation, soft agar colony formation and scratch closure assays. Effects on NFK beta expression and downstream targets including ABC transporters, BCL-xl and IAP were assessed by RT-PCR and western blotting. Treatment with 20 mu g/ml of Onconase significantly decreased cell count and invasion. Hsa-miR-17* was significantly upregulated and hsa-miR-30c was significantly downregulated by Onconase treatment in all cell lines. Forced expression of hsa-miR-17* mimic and hsa-miR-30c inhibitor each significantly decreased functional activity of Onconase in all assays. NFKB1 (p50) expression and downstream targets were also decreased with Onconase treatment, as well as with forced expression of miRNA mimic and inhibitors. Onconase treatment caused a significant decrease in cell proliferation, invasion and in expression of certain miRNAs. Recapitulation of the resultant miRNA expression pattern with hsa-miR-17* mimic and hsa-miR-30c inhibitor resulted in downregulation of NFKB1 and reduced malignant behavior in functional assays. Thus, Onconase likely exerts its antitumor effect through these miRNAs. Oncogene (2011) 30, 2767-2777; doi: 10.1038/onc.2010.643; published online 14 February 2011
引用
收藏
页码:2767 / 2777
页数:11
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