2016
MiR-205 functions as a tumor suppressor in adenocarcinoma and an oncogene in squamous cell carcinoma of esophagus
HÉŽOVÁ, Renata; Alena KOVAŘÍKOVÁ; Josef SROVNAL; Milada ZEMANOVÁ; Tomáš HARUSTIAK et. al.Základní údaje
Originální název
MiR-205 functions as a tumor suppressor in adenocarcinoma and an oncogene in squamous cell carcinoma of esophagus
Autoři
HÉŽOVÁ, Renata (203 Česká republika, domácí); Alena KOVAŘÍKOVÁ (203 Česká republika, domácí); Josef SROVNAL (203 Česká republika); Milada ZEMANOVÁ (203 Česká republika); Tomáš HARUSTIAK (703 Slovensko); Jiří EHRMANN (203 Česká republika); Marian HAJDÚCH (203 Česká republika); Milana ŠACHLOVÁ (203 Česká republika); Marek SVOBODA (203 Česká republika) a Ondřej SLABÝ (203 Česká republika, garant, domácí)
Vydání
Tumor Biology, Dordrecht, Springer, 2016, 1010-4283
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.650
Kód RIV
RIV/00216224:14740/16:00088840
Organizační jednotka
Středoevropský technologický institut
UT WoS
000376464700100
EID Scopus
2-s2.0-84951915614
Klíčová slova anglicky
Esophageal adenocarcinoma; Esophageal squamous cell carcinoma; miR-205; Tumor suppressor; Oncogene
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 27. 4. 2017 13:03, Mgr. Eva Špillingová
Anotace
V originále
Esophageal cancer is a malignant disease with poor prognosis, increasing incidence, and ineffective treatment options. MicroRNAs are post-transcriptional regulators of gene expression involved in many biological processes including carcinogenesis. We determined miR-205 expression levels in tumor/non-tumor tissues of 45 esophageal cancer patients using qPCR and found that decreased level of miR-205 in tumor tissue correlates with poor overall survival in esophageal adenocarcinoma patients. Further, we observed significantly higher levels of miR-205 in tumor tissue of esophageal squamous cell carcinoma. Ectopic overexpression of miR-205 in adenocarcinoma cell line SK-GT-4 led to decreased cell proliferation, cell cycle arrest in G1, and decreased migration ability. Conversely, in squamous cell line KYSE-150, same effects like inhibition of proliferation, migration, and colony-forming potential and cell cycle arrest in G2 were observed after silencing of miR-205. We performed global gene expression profiling and revealed that suppressive functioning of miR-205 in adenocarcinoma could be realized through regulation of epithelial-mesenchymal transition (EMT), whereas oncogenic in squamous cell carcinoma by regulation of metalloproteinase 10. Our results suggest that miR-205 could serve as biomarker in esophageal cancer and acts as a tumor suppressor in esophageal adenocarcinoma and oncogene in esophageal squamous cell carcinoma.
Návaznosti
ED1.1.00/02.0068, projekt VaV |
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NT13547, projekt VaV |
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NV15-34678A, projekt VaV |
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