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The association between the expression of solute carrier transporters and the prognosis of pancreatic cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F13%3A00071472" target="_blank" >RIV/00216224:14110/13:00071472 - isvavai.cz</a>

  • Alternative codes found

    RIV/65269705:_____/13:#0002129 RIV/00023001:_____/13:00058644 RIV/75010330:_____/13:00010098 RIV/00216208:11120/13:43907545 and 2 more

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s00280-013-2246-2" target="_blank" >http://dx.doi.org/10.1007/s00280-013-2246-2</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00280-013-2246-2" target="_blank" >10.1007/s00280-013-2246-2</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The association between the expression of solute carrier transporters and the prognosis of pancreatic cancer

  • Original language description

    The aim of this study was to investigate the prognostic significance of fourteen anticancer drug-relevant solute carrier transporters (SLCs) in pancreatic cancer in the context of clinical-pathological characteristics and the KRAS mutation status of tumors. Tumors and non-neoplastic pancreatic tissues were obtained from 32 histologically verified patients with pancreatic ductal adenocarcinoma. The transcript profile of SLCs was assessed using quantitative real-time PCR. KRAS mutations in exon 2 were assessed by high-resolution melting analysis and confirmed by sequencing. SLC22A3 and SLC22A18 were upregulated and SLC22A1, SLC22A2, SLC22A11, SLC28A1, SLC28A3 and SLC29A1 were downregulated when compared with non-neoplastic pancreatic tissues. Moreover, significantly lower levels of SLC22A1, SLC22A11 and SLC29A1 were found in tumors with angioinvasion. There was also a significantly higher transcript level of SLC28A1 in tumors with regional lymph nodes affected by metastasis.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    CANCER CHEMOTHERAPY AND PHARMACOLOGY

  • ISSN

    0344-5704

  • e-ISSN

  • Volume of the periodical

    72

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    14

  • Pages from-to

    669-682

  • UT code for WoS article

    000323653600019

  • EID of the result in the Scopus database