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CD markers variations in chronic lymphocytic leukemia: New insights into prognosis

Chronic lymphocytic leukemia (CLL) is one of the most commonly occurring adult leukemias that is associated with clonal accumulation of mature apoptosis‐resistant B‐cells in bone marrow, peripheral blood, and specific tissues. Different pathogenesis factors can contribute to the aggression of the cl...

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Bibliographic Details
Published in:Journal of cellular physiology 2019-11, Vol.234 (11), p.19420-19439
Main Authors: Vosoughi, Tina, Bagheri, Marziye, Hosseinzadeh, Mehran, Ehsanpour, Ali, Davari, Nader, Saki, Najmaldin
Format: Article
Language:English
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Summary:Chronic lymphocytic leukemia (CLL) is one of the most commonly occurring adult leukemias that is associated with clonal accumulation of mature apoptosis‐resistant B‐cells in bone marrow, peripheral blood, and specific tissues. Different pathogenesis factors can contribute to the aggression of the clinical course in this disease. Cytogenetic abnormalities and surface biomarkers of neoplastic CLL cells can be effective in the outcome of CLL, and the examination of changing CD markers expressions in the progression of CLL can be related to the prognosis of this disease. Changing expression levels of CD markers on lymphocytes and other cells in CLL patients can play a role in the aggressive clinical outcomes such as organomegaly, immunodeficiency, and advanced disease stages through their interaction with CLL microenvironment. Given the involvement of CD markers in the pathogenesis of CLL, it can be stated that recognizing the expression changes of CD markers in the cells involved in CLL can be a proper approach to evaluate prognosis among these patients. Chronic lymphocytic leukemia (CLL) is one of the most commonly occurring adult leukemias that various pathogenesis factors can contribute to the aggression of the clinical course in this disease. The examination of changing CD markers expressions as one of these factors can be related to the prognosis of CLL.
ISSN:0021-9541
1097-4652
DOI:10.1002/jcp.28724