Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0023418 (
leukemia
)
93,477
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
This study was aimed to investigate various factors influencing long-term survival in adult AML patients with fusion gene
aml1
/eto positive. A single institutional retrospective study with long-term follow-up was performed to better define the prognostic factors for AML patients with
aml1
/eto positive. Newly diagnosed 89 adult AML patients with
aml1
/eto positive were followed up for 1 to 42 months (median 24 months) from January 2004 to July 2008. Univariate and multivariate analysis of potential factors influencing survival and prognosis were carried out by using Log-Rank and Cox regression method, including sex, age, initial WBC counts, extramedullary leukemic disease, central nervous system
leukemia
(CNSL), chromosome aberrations, immunophenotype, first induction regimen, chemotherapy course to complete remission (CR), time from induction therapy to CR, negative or positive rate of
aml1
/eto and allogeneic hematopoietic stem cell transplantation and so on. The results showed that the estimated 5-year overall survival (OS) and relapse-free survival (RFS) were (50.0 +/- 2.3)% and (47.0 +/- 1.9)% respectively in follow-up of 89 patients for 1 - 42 months (mean 24 months). Univariate analysis revealed that initial WBC counts, CNSL, chemotherapy course to CR, time from induction therapy to CR, persistent negative in remission and allogeneic hematopoietic stem cell transplantation were important prognostic factors for long-term surviva1. Multivariate study demonstrated that initial WBC counts, CNSL, CD56 positive, negative or positive rate of
aml1
/eto, time from induction therapy to CR, persistent negative result of RT-PCR assay in remission and allogeneic hematopoietic stem cell transplantation were all critical factors in relation to OS and RFS. It is concluded that Chinese adult AML patients with fusion gene
aml1
/eto positive have some different characteristics as compared with patients from other countries, a relatively poor outcome is observed in patients, HSCT should be recommended to adult AML patients.
...
PMID:[Long-term survival analysis in 89 adult patients with acute myeloid leukemia of fusion gene aml1/eto positive]. 1954 1
The aim of study was to investigate the application of a novel microarray approach for the eight most common
leukemia
translocations in children for routine molecular diagnostic hematopathology practice. Bone marrow samples from 84 children with
leukemia
were analyzed by multiplex nested RT-PCR combined with oligonucleotide microarray. The results showed that out of 84 leukemic samples, 31 (36. 90%) carried 8 types of fusion genes including tel/
aml1
, e2a/pbx1, bcr/ablp190, bcr/ablp210, mll/af4,
aml1
/eto, pml/raralpha, cbfbeta/myh11. The sensitivity and specificity of the assay is comparable with the RT-PCR technique. In conclusion, this multiplex nested RT-PCR could quickly screen 8 types of chromosome structural aberrations at the same time. It can provide reliable and helpful information for risk stratification, therapy evaluation and prognosis prediction in childhood
leukemia
. There are both advantages and disadvantages in applying this new method. The microarray-based assay will be an effective and reliable tool in the clinical screening of
leukemia
patients for the presence of specific gene rearrangements with important diagnostic and prognostic implications.
...
PMID:[Identification of gene rearrangements in childhood leukemia by using a multiplex polymerase chain reaction-microarray approach]. 1969 27
Acute leukemia, the most common cancer in childhood, affects children's health severely, whereas the pathogeny and mechanism have not been elucidated clearly yet. As many studies showed, it has been found that transformation of cytogenetics plays a crucial role in
leukemia
development, and is frequently involved in the transforming action of
aml1
gene, one of which is essential for regulation of normal hematogenesis. Moreover, in children acute leukemia, more than one third children with acute leukemia can be detected with dysfunction of the
aml1
gene. Our findings highlight the translocation of
aml1
gene in children acute leukemia, indicating its mechanism, especailly provide a new target for clinical diagnosis and therapy. In this review, the structure and function of
aml1
gene, the abnormality of
aml1
gene in acute lymphocytic leukemia, abnormality of
aml1
gene in acute myeloid leukemia and so on were summarized.
...
PMID:[Aml1 gene abnormality in pediatric acute leukemia-review]. 1969 65
In presented work, new approach for the control of
aml1
/eto gene expression in t(8;21)(q22;q22)-positive acute myeloid leukemia cells has been developed. The technique is based on using the RNA-interference and lentiviral transduction methodology. Two new lentiviral vector sets for induction of constitutive anti-
aml1
/eto RNA-interference in acute myeloid leukemia cells have been developed and tested. The first set was based on use of artificial microRNAs (miRNAs) and second one was intended for production of short hairpin RNAs (shRNAs). It was shown that Kasumi-1 and SKNO-1
leukemia
cells can be efficiency transduced by each new lentiviral vector. Moreover, the percent of modified
leukemia
cells that may be easily evaluated in multiplicity of infection (MOI) test achieved more than 90% for Kasumi-1 and SKNO-1 cells at MOI 40 and 20, respectively. Comparative study elucidated that the anti-
aml1
/eto shRNA-based approach induced a stronger knock-down of
aml1
/eto gene in Kasumi-1 and SKNO-1 cells than the miRNA-based method did. We hope that the proposed approach may become useful instrument for controlling the
aml1
/eto gene expression in vitro as well as in vivo investigations of function and biological role of the gene.
...
PMID:[Effective and specific control of aml1/eto gene expression in acute myeloid leukemia cells by lentivecior-based RNA-interference]. 2163 21