cd56 antigen
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Author(s):  
Jurijs Nazarovs ◽  
Regīna Kleina ◽  
Sandra Lejniece

Abstract CD56, p53, and Cyclin D1 detection in plasma cells (PC) can help to predict prognosis of multiple myeloma (MM). Clinical and biochemical prognostic parameters were analysed in a group of 122 patients with primary diagnosed MM in the period 2011–2015. Bone marrow biopsies were analysed with Cyclin D1, p53, CD56 antibodies. Statistical analysis was performed using Microsoft Excel 2010 and Graph Pad Prism 5. Lack of CD56 expression and p53-positivity were significantly correlated with a low glomerular filtration rate (GFR), low platelet count and haemoglobin level, as well as with high serum creatinine levels. Patients with Cyclin D1 expression in PC had a significantly higher serum calcium level and more common osteolytic lesion in bones. CD56-negative as well as p53, Cyclin D1-positive groups had advanced Salmon–Durie MM stages by and significantly higher ß2-microglobulin. Expression of p53, Cyclin D1 and lack of CD56 antigen in PC are negative predictive factors in cases of MM, as these patients were diagnosed as having late Salmon–Durie stage and higher ß2-microglobulin level. Expression of p53 and lack of CD56 antigen in PC is associated with an increased creatinine level in blood and decreased GFR; therefore, these are criteria for chronic renal failure progression and poorer prognosis of MM.


2011 ◽  
Vol 29 (3) ◽  
pp. 2077-2082 ◽  
Author(s):  
Irena Djunic ◽  
Marijana Virijevic ◽  
Vladislava Djurasinovic ◽  
Aleksandra Novkovic ◽  
Natasa Colovic ◽  
...  

2011 ◽  
Vol 33 (3) ◽  
pp. 202-206 ◽  
Author(s):  
Ana Paula Alegretti ◽  
Christina Matzenbacher Bittar ◽  
Rosane Bittencourt ◽  
Amanda Kirchner Piccoli ◽  
Laiana Schneider ◽  
...  

2010 ◽  
Vol 92 (2) ◽  
pp. 306-313 ◽  
Author(s):  
Dong Wook Jekarl ◽  
Myungshin Kim ◽  
Jihyang Lim ◽  
Yonggoo Kim ◽  
Kyungja Han ◽  
...  

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4677-4677
Author(s):  
Bing Xu ◽  
Xiaoyan Song ◽  
Pengcheng Shi ◽  
Pengnan Xiao ◽  
Zhengshan Yu ◽  
...  

Abstract Abstract 4677 Introdution The expression of CD56 antigen and over-expression of the multidrug resistance gene 1 (MDR1) seems to confer the poor therapeutic outcome to AML. The aim of this study is to investigate the relationship between CD56 antigen expression and MDR1 gene expression in patients with de novo AML and explore the indicating effect of these two factors on clinical drug resistance. Patients and methods A real-time quantitative reverse transcriptase polymerase chain reaction method was established for detecting MDR1 expression levels and a three-color flow cytometry analysis with CD45/SSC gating was used to examine CD56 antigen expression in 79 patients with de novo AML. Results CD56 antigen was recorded in 19 out of 79 cases (24.1%) and particularly in those with M5 subtype and t(8;21) AML. Moreover, CD56 expression was significantly associated with unfavorable cytogenetic abnormalities (P< 0.05). Significantly higher percentage (57.1%, 4/7) of patients with t(8;21) demonstrated CD56 expression than those with favorable cytogenetic abnormalities (P< 0.05). CD56+ AML patients had higher incidence of splenohepatomegalia and level of lactate dehydrogenase than CD56- patients (P< 0.05). The median expression level of MDR1 was statistically higher in CD56+ AML patients than that in CD56- cases (P< 0.001) and 89.5% (17/19) CD56+ AML patients were found with high MDR1 expression. The CR rate in high MDR1 / CD56+ AML patients was significantly lower than that in low MDR1/ CD56- cases. (58.8% vs 89.2%, P< 0.01). Conclusions There is a linear correlation between MDR1 and CD56 expression in AML. This relationship may explain why CD56 expression is related to a poor prognosis in AML. Therefore both with high MDR1 expression level and CD56 antigen expression can identify AML patients with unfavorable outcome. Disclosures: No relevant conflicts of interest to declare.


2004 ◽  
Vol 45 (9) ◽  
pp. 1783-1789 ◽  
Author(s):  
Shigeki Ito ◽  
Yoji Ishida ◽  
Tatsuo Oyake ◽  
Mamiko Satoh ◽  
Yusei AOKI ◽  
...  

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