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Dysregulation of KRAS signaling in pancreatic cancer is not associated with KRAS mutations and outcome

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LEMSTROVA Radmila BRYNYCHOVA Veronika HUGHES David J. HLAVAS Viktor DVORAK Pavel DOHERTY Joanne E. MURRAY Helena A. CROCKARD Martin OLIVERIUS martin HLAVSA Jan HONSOVA Eva MAZANEC Jan KALA Zdeněk LOVECEK Martin HAVLIK Roman EHRMANN Jiri STROUHAL Ondrej SOUCEK Pavel MELICHAR Bohuslav MOHELNIKOVA-DUCHONOVA Beatrice

Rok publikování 2017
Druh Článek v odborném periodiku
Časopis / Zdroj Oncology Letters
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
Doi http://dx.doi.org/10.3892/ol.2017.6946
Obor Chirurgie včetně transplantologie
Klíčová slova pancreatic ductal adenocarcinoma; KRAS; gene expression; mutation; overall survival
Popis Pancreatic ductal adenocarcinoma (PDAC) is a tumor with a poor prognosis, and no targeted therapy is currently available. The aim of the present study was to investigate the prognostic significance of the expression of V-Ki-ras2 kirsten rat sarcoma viral oncogene homolog (KRAS), downstream signaling pathway genes and the association with clinical characteristics in PDAC patients undergoing radical surgery. Tumors and adjacent non-neoplastic pancreatic tissues were examined in 45 patients with histologically verified PDAC. KRAS and B-Raf proto-oncogene, serine/threonine kinase (BRAF) gene mutation analysis was performed using the KRAS/BRAF/phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha array.

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