The Tumor Suppressor MicroRNA-1 Exhibits Restricted Inhibition of Proliferation of Ovarian Cancer Cells

被引:0
|
作者
Stope, Matthias B. [1 ]
Hettenbach, Daria [2 ]
Kaul, Anne [2 ]
Paditz, Madeleine [2 ]
Diesing, Karoline [2 ]
Burchardt, Martin [1 ]
Zygmunt, Marek [2 ]
Mustea, Alexander [2 ]
Koensgen, Dominique [2 ]
机构
[1] Univ Med Greifswald, Dept Urol, Ferdinand Sauerbruch Str, D-17475 Greifswald, Germany
[2] Univ Med Greifswald, Dept Gynecol & Obstet, Greifswald, Germany
关键词
Ovarian cancer; microRNA miR-1; tumor suppressor; proliferation; MESENCHYMAL TRANSITION; TARGETING TAGLN2; DOWN-REGULATION; MIR-1; EXPRESSION; DIFFERENTIATION; IDENTIFICATION; APOPTOSIS; INVASION; MIRNAS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: MicroRNAs are able to control vital tumor biological processes, such as proliferation, tissue transformation and cell migration, as well as apoptosis. One of the micro RNAs, namely miR-1, has been classified as a tumor suppressor, however, preliminary data did not confirm this finding in ovarian cancer (OC) cells. This study examined the impact of miR-1 on OC cell growth. Materials and Methods: Recombinant miR-1 was overexpressed in human OC cell lines OVCAR-3, SK-OV-3, TOV-112D, and TOV-21G. Subsequently, cell growth was analyzed. Results: After transfection, 11- to 487-fold overexpression of miR-1 was detectable in the OC cells. However, no significant differences in proliferation compared to control cells were detected, neither in transiently nor in stably transfected cells. Conclusion: In numerous cancer entities miR-1 is defined as an antiproliferative tumor suppressor. Notably, the present study demonstrated a loss of growth-inhibitory functionality of miR-1 by so far unknown mechanisms, suggesting dysregulated miR-1 signaling or effector cascades in OC cells.
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页码:3329 / 3334
页数:6
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