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Hedgehog pathway overexpression in pancreatic cancer is abrogated by new-generation taxoid SB-T-1216
B. Mohelnikova-Duchonova, M. Kocik, B. Duchonova, V. Brynychova, M. Oliverius, J. Hlavsa, E. Honsova, J. Mazanec, Z. Kala, I. Ojima, DJ. Hughes, JE. Doherty, HA. Murray, MA. Crockard, R. Lemstrova, P. Soucek,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
NV16-28375A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
NLK
ProQuest Central
od 2001-01-01 do Před 1 rokem
Open Access Digital Library
od 2001-01-01
Health & Medicine (ProQuest)
od 2001-01-01 do Před 1 rokem
PubMed
27573236
DOI
10.1038/tpj.2016.55
Knihovny.cz E-zdroje
- MeSH
- duktální karcinom slinivky břišní farmakoterapie genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace MeSH
- myši nahé MeSH
- nádory slinivky břišní farmakoterapie genetika MeSH
- přežití bez známek nemoci MeSH
- proteiny hedgehog genetika MeSH
- protoonkogenní proteiny p21(ras) genetika MeSH
- senioři MeSH
- taxoidy aplikace a dávkování terapeutické užití MeSH
- transkriptom účinky léků MeSH
- výsledek terapie MeSH
- xenogenní modely - testy protinádorové aktivity MeSH
- zvířata MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The Hedgehog pathway is one of the major driver pathways in pancreatic ductal adenocarcinoma. This study investigated prognostic importance of Hedgehog signaling pathway in pancreatic cancer patients who underwent a radical resection. Tumors and adjacent non-neoplastic pancreatic tissues were obtained from 45 patients with histologically verified pancreatic cancer. The effect of experimental taxane chemotherapy on the expression of Hedgehog pathway was evaluated in vivo using a mouse xenograft model prepared using pancreatic cancer cell line Paca-44. Mice were treated by experimental Stony Brook Taxane SB-T-1216. The transcript profile of 34 Hedgehog pathway genes in patients and xenografts was assessed using quantitative PCR. The Hedgehog pathway was strongly overexpressed in pancreatic tumors and upregulation of SHH, IHH, HHAT and PTCH1 was associated with a trend toward decreased patient survival. No association of Hedgehog pathway expression with KRAS mutation status was found in tumors. Sonic hedgehog ligand was overexpressed, but all other downstream genes were downregulated by SB-T-1216 treatment in vivo. Suppression of HH pathway expression in vivo by taxane-based chemotherapy suggests a new mechanism of action for treatment of this aggressive tumor.
Department of Surgery University Hospital and Medical Faculty Masaryk University Brno Czech Republic
Department of Toxicogenomics National Institute of Public Health Prague Czech Republic
Citace poskytuje Crossref.org
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- $a The Hedgehog pathway is one of the major driver pathways in pancreatic ductal adenocarcinoma. This study investigated prognostic importance of Hedgehog signaling pathway in pancreatic cancer patients who underwent a radical resection. Tumors and adjacent non-neoplastic pancreatic tissues were obtained from 45 patients with histologically verified pancreatic cancer. The effect of experimental taxane chemotherapy on the expression of Hedgehog pathway was evaluated in vivo using a mouse xenograft model prepared using pancreatic cancer cell line Paca-44. Mice were treated by experimental Stony Brook Taxane SB-T-1216. The transcript profile of 34 Hedgehog pathway genes in patients and xenografts was assessed using quantitative PCR. The Hedgehog pathway was strongly overexpressed in pancreatic tumors and upregulation of SHH, IHH, HHAT and PTCH1 was associated with a trend toward decreased patient survival. No association of Hedgehog pathway expression with KRAS mutation status was found in tumors. Sonic hedgehog ligand was overexpressed, but all other downstream genes were downregulated by SB-T-1216 treatment in vivo. Suppression of HH pathway expression in vivo by taxane-based chemotherapy suggests a new mechanism of action for treatment of this aggressive tumor.
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