Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

MLL-Aberrations, Associated to T-AML, Are Induced by Chemotherapy In Vivo.

View through CrossRef
Abstract Background: Therapy related acute myelogenous leukemias (t-AML) are frequently observed following previous chemotherapy with alkylating agents and topoisomerase II-inhibitors (topo II-i.). Their incidence ranges between 5 – 15% in non-myeloablative and myeloablative treatment protocols respectively. T-AML after topo II-i. therapy often exhibit balanced MLL/11q23 translocations, e.g. t(9;11) and t(11;19). It is thought that the first step to induce MLL translocations is breakage and illegitimate recombination at the MLL breakpoint cluster region (bcr), which can be detected by genomic MLL-inverse PCR in vitro (Libura et al. 2004, Blood). The aim of this study was to detect the induction of MLL-aberrations in vivo after topo II-i. containing treatment regimens, using RT- and genomic inverse PCR (iPCR) and evaluate this information for early recognition of t-AML. Material and Methods: Patients with non-Hodgkin’s lymphoma, treated by intermediate or high dose chemotherapy, (MegaCHOEP protocol of the DSNHL) were enrolled. 216 samples of 75 patients were taken as peripheral blood (PB) after informed consent according to the convention of Helsinki. Peripheral blood of healthy adult donors were used as control. Blood samples were subjected either to a nested t(9;11) and t(11;19) RT- PCR or the genomic MLL-iPCR allowing detection of non specific aberrations in the MLL breakpoint cluster region. iPCR was carried out as described (Libura et al.). Processing of samples was carried out according to GLP guidelines for PCR. Results: 215 samples of 76 patients, taken at different time points of therapy have been investigated. The incidence of the t(9;11) and t(11,19) ranges between 0,5% (1/216) and 9,7% (21/216) of all samples and 1,3% (1/76) and 27,6% (21/76) of all patients. There was a tendency towards a higher incidence of these aberrations in patients which have completed therapy. Pretherapeutic samples were always PCR-negative and none of the patients has developed a t-AML so far. A total of 36 samples (18 healthy subjects, 18 patients) were subjected to MLL-iPCR. Surprisingly, the incidence of MLL-aberrations (deletions, insertions) in the healthy cohort was comparable to that of the patients’ samples (14/18 vs.12/18). We speculated that MLL-aberrations ex vivo might correlate with spontaneous apoptosis. We studied 10 samples of healthy donors at 0, 24 and 48h after having taken the sample. MLL-aberrations were not observed at 0 hrs, but emerged in 5/10 and 7/10 samples after 24 and 48h, respectively. Conclusion: These results show, that chemotherapy seems to induce the emergence of the t-AML associated MLL-translocations t(9;11) and t(11;19). Since their incidence exceeds the incidence of t-AML, characterized by these translocations, most of the positive PCR-results seem to represent a transient chemotherapy induced genetic instability and not a t-AML in a preleukemic phase. The genomic MLL iPCR is currently used for the detection of chemotherapy-induced MLL-genomic aberrations. Our results indicate, that apoptosis might induce aberrations in the MLL bcr, which need to be discerned from those which are provoked by chemotherapy.
Title: MLL-Aberrations, Associated to T-AML, Are Induced by Chemotherapy In Vivo.
Description:
Abstract Background: Therapy related acute myelogenous leukemias (t-AML) are frequently observed following previous chemotherapy with alkylating agents and topoisomerase II-inhibitors (topo II-i.
).
Their incidence ranges between 5 – 15% in non-myeloablative and myeloablative treatment protocols respectively.
T-AML after topo II-i.
therapy often exhibit balanced MLL/11q23 translocations, e.
g.
t(9;11) and t(11;19).
It is thought that the first step to induce MLL translocations is breakage and illegitimate recombination at the MLL breakpoint cluster region (bcr), which can be detected by genomic MLL-inverse PCR in vitro (Libura et al.
2004, Blood).
The aim of this study was to detect the induction of MLL-aberrations in vivo after topo II-i.
containing treatment regimens, using RT- and genomic inverse PCR (iPCR) and evaluate this information for early recognition of t-AML.
Material and Methods: Patients with non-Hodgkin’s lymphoma, treated by intermediate or high dose chemotherapy, (MegaCHOEP protocol of the DSNHL) were enrolled.
216 samples of 75 patients were taken as peripheral blood (PB) after informed consent according to the convention of Helsinki.
Peripheral blood of healthy adult donors were used as control.
Blood samples were subjected either to a nested t(9;11) and t(11;19) RT- PCR or the genomic MLL-iPCR allowing detection of non specific aberrations in the MLL breakpoint cluster region.
iPCR was carried out as described (Libura et al.
).
Processing of samples was carried out according to GLP guidelines for PCR.
Results: 215 samples of 76 patients, taken at different time points of therapy have been investigated.
The incidence of the t(9;11) and t(11,19) ranges between 0,5% (1/216) and 9,7% (21/216) of all samples and 1,3% (1/76) and 27,6% (21/76) of all patients.
There was a tendency towards a higher incidence of these aberrations in patients which have completed therapy.
Pretherapeutic samples were always PCR-negative and none of the patients has developed a t-AML so far.
A total of 36 samples (18 healthy subjects, 18 patients) were subjected to MLL-iPCR.
Surprisingly, the incidence of MLL-aberrations (deletions, insertions) in the healthy cohort was comparable to that of the patients’ samples (14/18 vs.
12/18).
We speculated that MLL-aberrations ex vivo might correlate with spontaneous apoptosis.
We studied 10 samples of healthy donors at 0, 24 and 48h after having taken the sample.
MLL-aberrations were not observed at 0 hrs, but emerged in 5/10 and 7/10 samples after 24 and 48h, respectively.
Conclusion: These results show, that chemotherapy seems to induce the emergence of the t-AML associated MLL-translocations t(9;11) and t(11;19).
Since their incidence exceeds the incidence of t-AML, characterized by these translocations, most of the positive PCR-results seem to represent a transient chemotherapy induced genetic instability and not a t-AML in a preleukemic phase.
The genomic MLL iPCR is currently used for the detection of chemotherapy-induced MLL-genomic aberrations.
Our results indicate, that apoptosis might induce aberrations in the MLL bcr, which need to be discerned from those which are provoked by chemotherapy.

Related Results

Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Objective: To determine the frequency of common chromosomal aberrations in local population idiopathic determine the frequency of common chromosomal aberrations in local population...
Abstract B35: Estradiol drives MLL gene fusions in infant acute leukemia
Abstract B35: Estradiol drives MLL gene fusions in infant acute leukemia
Abstract Translocation breakpoints involving the MLL gene linked to Infant Acute Leukemia (IAL) and therapy related acute leukemia (tAL) are tightly clustered betwee...
Abstract 4345: Epigenetic dysregulation of transcriptional program in MLL-EEN leukemia
Abstract 4345: Epigenetic dysregulation of transcriptional program in MLL-EEN leukemia
Abstract Aberrant DNA methylation is a typical feature of cancers, which is usually associated with deregulation of tumor suppressor genes and oncogenes. Mixed linea...
PRMT1 Activates Leukemic Stem Cell Program in MLL-Rearranged Leukemia
PRMT1 Activates Leukemic Stem Cell Program in MLL-Rearranged Leukemia
Abstract In MLL-rearranged leukemia, the Mixed Lineage Leukemia (MLL) gene undergoes chromosomal translocation that results in the loss of C-terminal histone methylt...
Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
Chromosomal rearrangements involving the MLL gene have been associated with many different types of hematological malignancies. Fluorescent in situ hybridization with a panel of pr...
Chemotherapy-Induced T-MDS/AML-Associated Genetic Aberrations.
Chemotherapy-Induced T-MDS/AML-Associated Genetic Aberrations.
Abstract Therapy-related solid and hematological neoplasias occur according to the treatment regimen and intensity. The cumulative incidence of therapy related myelo...
The Role of MLL1 and MLL2 in MLL Fusion Oncoprotein-Initiated Leukemia
The Role of MLL1 and MLL2 in MLL Fusion Oncoprotein-Initiated Leukemia
Abstract The MLL1 histone methyltransferase gene at 11q23 undergoes many distinct chromosomal translocations to yield poor prognosis leukemia. In these MLL-rearrange...
Flt3 Is Required for MLL-ENL-Induced Leukemogenesis In Vivo, but Not for LSC Function in Vitro
Flt3 Is Required for MLL-ENL-Induced Leukemogenesis In Vivo, but Not for LSC Function in Vitro
Abstract Abstract 2450 Flt3 is a type III tyrosine kinase receptor expressed on hematopoietic multipotential progenitors and more downstream progenito...

Back to Top