2015
DOI: 10.1007/s13402-014-0215-3
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Molecular basis of chronic lymphocytic leukemia diagnosis and prognosis

Abstract: Specific chromosomal abnormalities and gene mutations may serve as diagnostic and prognostic indicators for disease progression and survival. The identification of these anomalies by state-of-the-art molecular (cyto)genetic techniques such as fluorescence in situ hybridization (FISH), comparative genomic hybridization (CGH), single nucleotide polymorphism (SNP) microarray-based genomic profiling and next-generation sequencing (NGS) can be of paramount help for the clinical management of these patients, includi… Show more

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Cited by 34 publications
(30 citation statements)
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“…CLL is the most common leukemia in middle age and is associated with abnormal proliferation of lymphocytes and their resistance to apoptosis [96]. About 60-65 % of CLL cases bear mutation in variable region of the immunoglobulin heavy chain (IGHV), which may change the affinity of B-cell receptor (BCR) for antigens.…”
Section: Chronic Lymphocytic Leukemia (Cll)mentioning
confidence: 99%
See 1 more Smart Citation
“…CLL is the most common leukemia in middle age and is associated with abnormal proliferation of lymphocytes and their resistance to apoptosis [96]. About 60-65 % of CLL cases bear mutation in variable region of the immunoglobulin heavy chain (IGHV), which may change the affinity of B-cell receptor (BCR) for antigens.…”
Section: Chronic Lymphocytic Leukemia (Cll)mentioning
confidence: 99%
“…Twist-2 promoter in CLL patients with mutated IGHV (associated with favorable prognosis) is largely methylated, which results in silencing of TWIST-2 genes in these patients, while Twist2 is expressed in unmutated subtypes [96,100]. Some studies suggest that the expression of Twist-2 in unmutated IGHV patients with unmethylated Twist-2 can interfere with P53 pathway, but it has not been proved yet.…”
Section: Chronic Lymphocytic Leukemia (Cll)mentioning
confidence: 99%
“…SmIgdim, CD5+, CD19+, CD20dim, CD23+) in peripheral blood, bone marrow, lymph nodes and other lymphoid tissues (Hodgson et al, 2011;Shahjahani et al, 2015). It is a heterogeneous disease with a variable clinical outcome (Mozaheb et al, 2012;.…”
Section: Introductionmentioning
confidence: 99%
“…Imatinib, a first generation TKI, is a 2-phenylamiropyrimidine (PAP) derivative that competitively blocks the adenosine triphosphate (ATP) binding site of the BCR-ABL fusion protein, thereby preventing ATP from interacting with its catalytic domain [152]. This inhibitory activity impairs BCR-ABL auto-phosphorylation and its downstream signaling, leading to reduced proliferation and apoptosis-mediated cell death.…”
Section: Targeting Leukemia Stem Cellsmentioning
confidence: 99%