Detail publikace

Comparative gene expression profiling of human metallothionein-3 up-regulation in neuroblastoma cells and its impact on susceptibility to cisplatin

MERLOS RODRIGO, M. DOSTÁLOVÁ, S. BUCHTELOVÁ, H. STRMISKA, V. MICHÁLEK, P. KŘÍŽKOVÁ, S. VÍCHA, A. JENČOVÁ, P. ECKSCHLAGER, T. STIBOROVÁ, M. HEGER, Z. ADAM, V.

Originální název

Comparative gene expression profiling of human metallothionein-3 up-regulation in neuroblastoma cells and its impact on susceptibility to cisplatin

Typ

článek v časopise ve Web of Science, Jimp

Jazyk

angličtina

Originální abstrakt

Human metallothionein-3 (hMT-3), also known as growth inhibitory factor, is predominantly expressed in the central nervous system. hMT-3 is presumed to participate in the processes of heavy metal detoxification, regulation of metabolism and protection against oxidative damage of free radicals in the central nervous system; thus, it could play important neuromodulatory and neuroprotective roles. However, the primary functions of hMT-3 and the mechanism underlying its multiple functions in neuroblastoma have not been elucidated so far. First, we confirmed relatively high expression of hMT-3 encoding mRNA in biopsies (n = 23) from high-risk neuroblastoma subjects. Therefore, we focused on investigation of the impact of hMT-3 up-regulation in N-Myc amplifying neuroblastoma cells. The differentially up-regulated genes involved in biological pathways related to cellular senescence and cell cycle were identified using electrochemical microarray with consequent bioinformatic processing. Further, as experimental verification of microarray data, the cytotoxicity of the cisplatin (CDDP) was examined in hMT-3 and mock cells by MTT and clonogenic assays. Overall, our data strongly suggest that up-regulation of hMT-3 positively correlates with the genes involved in oncogene-induced senescence (CDKN2B and ANAPC5) or apoptosis (CASP4). Moreover, we identified a significant increase in chemoresistance to cisplatin (CDDP) due to hMT-3 up-regulation (24IC(50): 7.5 vs. 19.8 mu g/ml), indicating its multipurpose biological significance.

Klíčová slova

apoptosis; cisplatin; chemoresistance; metallothionein; oncogene-induced senescence

Autoři

MERLOS RODRIGO, M.; DOSTÁLOVÁ, S.; BUCHTELOVÁ, H.; STRMISKA, V.; MICHÁLEK, P.; KŘÍŽKOVÁ, S.; VÍCHA, A.; JENČOVÁ, P.; ECKSCHLAGER, T.; STIBOROVÁ, M.; HEGER, Z.; ADAM, V.

Vydáno

12. 1. 2018

Nakladatel

Impact Journals

ISSN

1949-2553

Periodikum

Oncotarget

Ročník

9

Číslo

4

Stát

Spojené státy americké

Strany od

4427

Strany do

4439

Strany počet

13

URL

Plný text v Digitální knihovně

BibTex

@article{BUT145110,
  author="MERLOS RODRIGO, M. and DOSTÁLOVÁ, S. and BUCHTELOVÁ, H. and STRMISKA, V. and MICHÁLEK, P. and KŘÍŽKOVÁ, S. and VÍCHA, A. and JENČOVÁ, P. and ECKSCHLAGER, T. and STIBOROVÁ, M. and HEGER, Z. and ADAM, V.",
  title="Comparative gene expression profiling of human metallothionein-3 up-regulation in neuroblastoma cells and its impact on susceptibility to cisplatin",
  journal="Oncotarget",
  year="2018",
  volume="9",
  number="4",
  pages="4427--4439",
  doi="10.18632/oncotarget.23333",
  issn="1949-2553",
  url="http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=view&path[]=23333&path[]=73538"
}