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| Hauptseite > Publikationsdatenbank > Induction of the chromosomal translocation t(14;18) by targeting theBCL-2 locus with specific binding I-125-labeled Triplex-Forming oligonucleotides > print |
| Hauptseite > Publikationsdatenbank > Induction of the chromosomal translocation t(14;18) by targeting theBCL-2 locus with specific binding I-125-labeled Triplex-Forming oligonucleotides > print |
| 001 | 255692 | ||
| 005 | 20210129220524.0 | ||
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| 037 | _ | _ | |a FZJ-2015-05824 |
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| 100 | 1 | _ | |a Dahmen, Volker |0 P:(DE-Juel1)133468 |b 0 |u fzj |
| 111 | 2 | _ | |a 15th International Congress of Radiation Reasearch |g ICRR |c Kyoto |d 2015-05-25 - 2015-05-29 |w Japan |
| 245 | _ | _ | |a Induction of the chromosomal translocation t(14;18) by targeting theBCL-2 locus with specific binding I-125-labeled Triplex-Forming oligonucleotides |
| 260 | _ | _ | |c 2015 |
| 336 | 7 | _ | |a Conference Paper |0 33 |2 EndNote |
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| 520 | _ | _ | |a Triplex-Forming oligonucleotides (TFO) are able to bind DNA in a sequence specific manner and are a promising tool to manipulate genes or gene regulatory units in a cellular environment. TFO possess a therapeutic potential e.g. as a carrier molecule for Alpha- or Auger-Electron-Emitter (AEE) to target specific DNA sequences in tumor cells. We established a method for the effective labeling of TFO with the AEE Iodine-125 (I-125) and analyzed the influence of I-125-labeled TFO in SCL-II cells on gene expression and translocation frequency of the human BCL2 gene. The TFO-BCL2 employed in the present study binds to the BCL2 gene at approximately 5400 bp upstream of the 3´-end. TFO labeling with I-125 was performed using the primer extension method. SCL-II cells were transfected with TFO via electroporation and subsequently stored at -150°C for decay accumulation up to a range from 100 to 330 decays/cell. SCL-II cells either transfected with I-125-labeled multi-binding TFO (>300,000 targets per genome) or transfected with non-labeled TFO-BCL2 served as controls. Monitoring of BCL2 translocations was done with the Fluorescence-In-Situ-Hybridization (FISH) method. The utilized FISH probes were designed to detect a translocation of the BCL2 gene from chromosome 18 to chromosome 14, a common translocation found in follicular lymphomas leading to an overexpression of BCL-2 protein. Analysis of BCL2 gene expression levels was done via quantitative Real-Time PCR on the Real Time PCR System 7500 (Applied Biosystems).The relative gene expression of BCl-2 in I-125-TFO-BCL2 transfected cells showed a significant up-regulation when compared to the controls. Control SCL-II cells were either transfected with I-125-labeled multi-binding TFO (>300,000 targets per genome) or non-labeled TFO-BCL2. Analysis of the BCL2 t(14;18) translocation frequency revealed a significant 1.8- to 2-fold increase when compared to the control cells.We conclude that I-125 decays within the BCL2 gene facilitates the occurrence of the t(14;18) chromosomal translocation in SCL-II cells and that the increased translocation frequency of t(14;18) contributes to the observed overall enhanced BCL-2 expression. However, it seems unlikely that these rare translocation events fully explain the observed enhanced gene expression of BCL-2.Funded by Bundesministerium für Bildung und Forschung (BMBF), Grant 02NUK005A |
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| 700 | 1 | _ | |a Kriehuber, Ralf |0 P:(DE-Juel1)133469 |b 1 |e Corresponding author |u fzj |
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