Detailed Information on Publication Record
2014
MicroRNA-155 influences B-cell receptor signaling and associates with aggressive disease in chronic lymphocytic leukemia.
CUI, B., L. CHEN, S. ZHANG, Marek MRÁZ, J.F. FECTEAU et. al.Basic information
Original name
MicroRNA-155 influences B-cell receptor signaling and associates with aggressive disease in chronic lymphocytic leukemia.
Authors
CUI, B. (840 United States of America), L. CHEN (840 United States of America), S. ZHANG (840 United States of America), Marek MRÁZ (203 Czech Republic, guarantor, belonging to the institution), J.F. FECTEAU (840 United States of America), J. YU (840 United States of America), E.M. GHIA (840 United States of America), L. ZHANG (840 United States of America), L. BAO (840 United States of America), LZ. RASSENTI (840 United States of America), K. MESSER (840 United States of America), GA. CALIN (840 United States of America), CM. CROCE (840 United States of America) and TJ. KIPPS (840 United States of America)
Edition
Blood, USA, W.B. Saunders, 2014, 0006-4971
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 10.452
RIV identification code
RIV/00216224:14740/14:00078339
Organization unit
Central European Institute of Technology
UT WoS
000342619600018
Keywords in English
B-cell receptor; miR-155; chronic lymphocytic leukemia
Tags
Tags
International impact, Reviewed
Změněno: 11/3/2015 15:41, Martina Prášilová
Abstract
V originále
High-level leukemia cell expression of micro-RNA 155 (miR-155) is associated with more aggressive disease in patients with chronic lymphocytic leukemia (CLL), including those cases with a low-level expression of -chain-associated protein of 70 kD. CLL with high-level miR-155 expressed lower levels of Src homology-2 domain-containing inositol 5-phosphatase 1 and were more responsive to B-cell receptor (BCR) ligation than CLL with low-level miR-155. Transfection with miR-155 enhanced responsiveness to BCR ligation, whereas transfection with a miR-155 inhibitor had the opposite effect. CLL in lymphoid tissue expressed higher levels of miR155HG than CLL in the blood of the same patient. Also, isolated CD5(bright)CXCR4(dim) cells, representing CLL that had been newly released from the microenvironment, expressed higher levels of miR-155 and were more responsive to BCR ligation than isolated CD5(dim)CXCR4(bright) cells of the same patient. Treatment of CLL or normal B cells with CD40-ligand or B-cell-activating factor upregulated miR-155 and enhanced sensitivity to BCR ligation, effects that could be blocked by inhibitors to miR-155. This study demonstrates that the sensitivity to BCR ligation can be enhanced by high-level expression of miR-155, which in turn can be induced by crosstalk within the tissue microenvironment, potentially contributing to its association with adverse clinical outcome in patients with CLL.