2017
The association of miR-126-3p, miR-126-5p and miR-664-3p expression profiles with outcomes of patients with metastatic colorectal cancer treated with bevacizumab
FIALA, O., P. PITULE, P. HOSEK, V. LISKA, O. SOREJS et. al.Základní údaje
Originální název
The association of miR-126-3p, miR-126-5p and miR-664-3p expression profiles with outcomes of patients with metastatic colorectal cancer treated with bevacizumab
Autoři
FIALA, O. (203 Česká republika), P. PITULE (203 Česká republika), P. HOSEK (203 Česká republika), V. LISKA (203 Česká republika), O. SOREJS (203 Česká republika), J. BRUHA (203 Česká republika), O. VYCITAL (203 Česká republika), T. BUCHLER (203 Česká republika), Alexandr POPRACH (203 Česká republika, garant, domácí), O. TOPOLCAN (203 Česká republika) a J. FINEK (203 Česká republika)
Vydání
Tumor Biology, Dordrecht, Springer, 2017, 1010-4283
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 3.650 v roce 2016
Kód RIV
RIV/00216224:14110/17:00098712
Organizační jednotka
Lékařská fakulta
UT WoS
000407152800001
Klíčová slova anglicky
Colorectal cancer; bevacizumab; chemotherapy; microRNA; miR-126-3p; miR-126-5p; miR-664-3p
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 21. 3. 2018 16:16, Soňa Böhmová
Anotace
V originále
MicroRNAs regulate the expression of genes involved in several important cancer-related processes including cell adhesion, proliferation, and tumour angiogenesis. Bevacizumab is routinely used in the treatment of patients with metastatic colorectal cancer, but, so far, no reliable biomarker predicting response to bevacizumab has been established. The aim of our retrospective study was to evaluate the association of miR-126-3p, miR-126-5p and miR-664-3p tumour expression levels with outcomes of patients with metastatic colorectal cancer treated with bevacizumab. The study included 63 patients. For the assessment of microRNA expression, gene-specific TaqMan assays were used. The median progression-free survival and overall survival for patients with low tumour expression of miR-126-3p were 8.8 and 20.6 months versus 13.5 months and median overall survival was not reached for patients with high expression (p = 0.0064 and p = 0.0027), respectively. The median progression-free survival and overall survival for patients with low tumour expression of miR-126-5p were 9.0 and 22.2 months versus 12.0 and 23.4 months for patients with high expression (p = 0.2113 and 0.6858), respectively. The median progression-free survival and overall survival for patients with low tumour expression of miR-664-3p were 9.1 and 22.5 months versus 8.8 and 23.4 months for patients with high expression (p = 0.2542 and p = 0.1922), respectively. The multivariable Cox proportional hazards model revealed that miR-126-3p expression was significantly associated with progression-free survival (hazard ratio = 0.28, p = 0.0053) and also with overall survival (hazard ratio = 0.18, p = 0.0046). In conclusion, the results of this study suggest that the expression of miR-126-3p in the tumour tissue was associated with outcome of metastatic colorectal cancer patients treated with bevacizumab.