Hedgehog pathway overexpression in pancreatic cancer is abrogated by new-generation taxoid SB-T-1216
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F75010330%3A_____%2F17%3A00011803" target="_blank" >RIV/75010330:_____/17:00011803 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15110/16:33160468 RIV/65269705:_____/17:00067268 RIV/00023001:_____/17:00076157 RIV/00216224:14110/17:00098092 RIV/00216208:11120/17:43915997
Result on the web
<a href="http://www.nature.com/tpj/journal/v17/n5/full/tpj201655a.html" target="_blank" >http://www.nature.com/tpj/journal/v17/n5/full/tpj201655a.html</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/tpj.2016.55" target="_blank" >10.1038/tpj.2016.55</a>
Alternative languages
Result language
angličtina
Original language name
Hedgehog pathway overexpression in pancreatic cancer is abrogated by new-generation taxoid SB-T-1216
Original language description
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
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30101 - Human genetics
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Pharmacogenomics Journal
ISSN
1470-269X
e-ISSN
1473-1150
Volume of the periodical
17
Issue of the periodical within the volume
5
Country of publishing house
GB - UNITED KINGDOM
Number of pages
9
Pages from-to
452-460
UT code for WoS article
000411849200008
EID of the result in the Scopus database
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