| 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. |