dc.contributor.author |
Szász, Attila Marcell |
|
dc.contributor.author |
Ács, Balázs |
|
dc.contributor.author |
Ágoston, Emese |
|
dc.contributor.author |
Sztupinszki, Zsófia |
|
dc.contributor.author |
Tőkés, Anna-Mária |
|
dc.contributor.author |
Szittya Liliána |
|
dc.contributor.author |
Székely, Borbála |
|
dc.contributor.author |
Szendrői, Miklós |
|
dc.contributor.author |
Li Quiyuan |
|
dc.contributor.author |
Harsányi, László |
|
dc.contributor.author |
Tímár, József |
|
dc.contributor.author |
Szállási Zoltán |
|
dc.contributor.author |
Swanton Charles |
|
dc.contributor.author |
Győrffy, Balázs |
|
dc.contributor.author |
Kulka, Janina |
|
dc.date.accessioned |
2015-11-02T12:59:25Z |
|
dc.date.available |
2015-11-02T12:59:25Z |
|
dc.date.issued |
2013 |
|
dc.identifier |
84876267460 |
|
dc.identifier.citation |
pagination=627-632;
journalVolume=154;
journalIssueNumber=16;
journalTitle=ORVOSI HETILAP; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/423 |
|
dc.identifier.uri |
doi:10.1556/OH.2013.29590 |
|
dc.description.abstract |
Background: Grade 2 breast carcinomas do not form a uniform prognostic group. Aim: To extend the number of patients and the investigated genes of a previously identified prognostic signature described by the authors that reflect chromosomal instability in order to refine characterization of grade 2 breast cancers and identify driver genes. Methods: Using publicly available databases, the authors selected 9 target and 3 housekeeping genes that are capable to divide grade 2 breast carcinomas into prognostic groups. Gene expression was investigated by polymerase chain reaction in 249 formalin-fixed, paraffin-embedded breast tumors. The results were correlated with relapse-free survival. Results: Histologically grade 2 carcinomas were split into good and a poor prognosis groups. Centroid-based ranking showed that 3 genes, FOXM1, TOP2A and CLDN4 were able to separate the good and poor prognostic groups of grade 2 breast carcinomas. Conclusion: Using appropriately selected control genes, a limited set of genes is able to split prognostic groups of breast carcinomas independently from their grade. |
|
dc.relation.ispartof |
urn:issn:0030-6002 |
|
dc.title |
Egyszerűsített, alacsony költségű génexpressziós teszt az emlődaganatos betegségek kimenetelének előrejelzésére rutin patológiai blokkok felhasználásával |
|
dc.type |
Journal Article |
|
dc.date.updated |
2014-11-06T10:42:50Z |
|
dc.language.rfc3066 |
hu |
|
dc.identifier.mtmt |
2286072 |
|
dc.contributor.department |
SE/ÁOK/K/I. Sz. Sebészeti Klinika |
|
dc.contributor.department |
SE/ÁOK/I/IISZPI/MTA-SE Molekuláris Onkológia Kutatócsoport |
|
dc.contributor.department |
SE/ÁOK/K/ISZGYK/MTA-SE Gyermekgyógyászati és Nephrológiai Kutatócsoport |
|
dc.contributor.department |
SE/AOK/I/II. Sz. Patológiai Intézet |
|
dc.contributor.department |
SE/AOK/K/Ortopédiai Klinika |
|
dc.contributor.institution |
Semmelweis Egyetem |
|
dc.mtmt.swordnote |
Szász A. Marcell, Ács Balázs, Ágoston Emese szerzők egyenlő mértékben járultak hozzá a közleményhez. |
|