-
Je něco špatně v tomto záznamu ?
Serum levels of soluble adhesion molecules in newly diagnosed acute myeloid leukemia and in complete remission suggest endothelial cell activation by myeloblasts
T. Kupsa, J. Vanek, Z. Pavel, L. Jebavy, J. M. Horacek
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
27833171
DOI
10.5507/bp.2016.054
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie krev MeSH
- C-reaktivní protein metabolismus MeSH
- cytokiny metabolismus MeSH
- endoteliální buňky fyziologie MeSH
- indukce remise MeSH
- lidé středního věku MeSH
- lidé MeSH
- molekuly buněčné adheze metabolismus MeSH
- počet leukocytů MeSH
- prekurzorové buňky granulocytů fyziologie MeSH
- studie případů a kontrol MeSH
- vaskulární endoteliální růstový faktor A metabolismus MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND AND AIMS: Despite high-dose multi-agent chemotherapy and allogeneic stem cell transplantation, the relapse rate of acute myeloid leukemia (AML) is high. Further, the disease is highly resistent to drugs. We speculated that deeper understanding of AML-endothelial cell interactions might provide new targets for selective modulation of the AML microenvironment and form the basis for novel treatment approaches. In this study, we evaluated levels of endothelium derived soluble adhesion molecules in active disease and in complete remission (CR) and their relationship with inflammatory cytokines. METHODS: Baseline serum levels of 25 cytokines and 5 soluble adhesion molecules were measured in 84 AML patients using biochip array technology. CR samples were evaluated in 44 patients of this cohort. The control group consisted of 15 healthy blood donors. RESULTS: All analytes were independent of age or disease origin. Some correlations were restricted to active AML, some were ubiquitous and some were found in remission. In active disease, E-selectin (E-SEL) and VCAM-1 correlated with leukocyte count, E-SEL correlated with P-selectin (P-SEL). Platelet count related to IL-7, EGF and VEGF but not to P-SEL. In CR, P-SEL correlated with platelet count and EGF but not with E-SEL. There was no relationship of P-SEL and E-SEL in the control group. CONCLUSIONS: Leukemic activity is associated with a different pattern of soluble adhesion molecule levels. Both E-SEL and P-SEL may be derived from endothelial cells. Their levels correlated in active disease. E-SEL correlated with leukocyte count. In CR, P-SEL physiologically correlated with platelet count. The correlation with E-SEL was insignificant and absent in the control group. Our data suggest activation of endothelial cells in the presence of myeloblasts.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17032089
- 003
- CZ-PrNML
- 005
- 20200211141212.0
- 007
- ta
- 008
- 171025s2017 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.5507/bp.2016.054 $2 doi
- 035 __
- $a (PubMed)27833171
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Kupsa, Tomáš $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences (FMHS), Hradec Kralove, Czech Republic; 4th Department of Internal Medicine - Hematology, University Hospital Hradec Kralove, Czech Republic $7 xx0267991
- 245 10
- $a Serum levels of soluble adhesion molecules in newly diagnosed acute myeloid leukemia and in complete remission suggest endothelial cell activation by myeloblasts / $c T. Kupsa, J. Vanek, Z. Pavel, L. Jebavy, J. M. Horacek
- 520 9_
- $a BACKGROUND AND AIMS: Despite high-dose multi-agent chemotherapy and allogeneic stem cell transplantation, the relapse rate of acute myeloid leukemia (AML) is high. Further, the disease is highly resistent to drugs. We speculated that deeper understanding of AML-endothelial cell interactions might provide new targets for selective modulation of the AML microenvironment and form the basis for novel treatment approaches. In this study, we evaluated levels of endothelium derived soluble adhesion molecules in active disease and in complete remission (CR) and their relationship with inflammatory cytokines. METHODS: Baseline serum levels of 25 cytokines and 5 soluble adhesion molecules were measured in 84 AML patients using biochip array technology. CR samples were evaluated in 44 patients of this cohort. The control group consisted of 15 healthy blood donors. RESULTS: All analytes were independent of age or disease origin. Some correlations were restricted to active AML, some were ubiquitous and some were found in remission. In active disease, E-selectin (E-SEL) and VCAM-1 correlated with leukocyte count, E-SEL correlated with P-selectin (P-SEL). Platelet count related to IL-7, EGF and VEGF but not to P-SEL. In CR, P-SEL correlated with platelet count and EGF but not with E-SEL. There was no relationship of P-SEL and E-SEL in the control group. CONCLUSIONS: Leukemic activity is associated with a different pattern of soluble adhesion molecule levels. Both E-SEL and P-SEL may be derived from endothelial cells. Their levels correlated in active disease. E-SEL correlated with leukocyte count. In CR, P-SEL physiologically correlated with platelet count. The correlation with E-SEL was insignificant and absent in the control group. Our data suggest activation of endothelial cells in the presence of myeloblasts.
- 650 _2
- $a C-reaktivní protein $x metabolismus $7 D002097
- 650 _2
- $a studie případů a kontrol $7 D016022
- 650 _2
- $a molekuly buněčné adheze $x metabolismus $7 D015815
- 650 _2
- $a cytokiny $x metabolismus $7 D016207
- 650 _2
- $a endoteliální buňky $x fyziologie $7 D042783
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a prekurzorové buňky granulocytů $x fyziologie $7 D042381
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a akutní myeloidní leukemie $x krev $7 D015470
- 650 _2
- $a počet leukocytů $7 D007958
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a indukce remise $7 D012074
- 650 _2
- $a vaskulární endoteliální růstový faktor A $x metabolismus $7 D042461
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Vaněk, Jan, $u Department of Informatics and Quantitative Methods, Faculty of Informatics and Management, University of Hradec Kralove, Hradec Kralove, Czech Republic $d 1978- $7 xx0114510
- 700 1_
- $a Žák, Pavel, $u 4th Department of Internal Medicine - Hematology, University Hospital Hradec Kralove, Czech Republic; 4th Department of Internal Medicine - Hematology, Faculty of Medicine, Charles University in Prague, Hradec Kralove, Czech Republic $d 1966- $7 mzk2006354145
- 700 1_
- $a Jebavý, Ladislav, $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences (FMHS), Hradec Kralove, Czech Republic; 4th Department of Internal Medicine - Hematology, University Hospital Hradec Kralove, Czech Republic $d 1950- $7 mzk2007408362
- 700 1_
- $a Horáček, Jan $u Department of Military Internal Medicine and Military Hygiene, University of Defence, Faculty of Military Health Sciences (FMHS), Hradec Kralove, Czech Republic; 4th Department of Internal Medicine - Hematology, University Hospital Hradec Kralove, Czech Republic $7 xx0040415
- 773 0_
- $w MED00012606 $t Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czech Republic $x 1213-8118 $g Roč. 161, č. 1 (2017), s. 92-99
- 910 __
- $a ABA008 $b A 1502 $c 958 $y 4 $z 0
- 990 __
- $a 20171025 $b ABA008
- 991 __
- $a 20200211141606 $b ABA008
- 999 __
- $a ok $b bmc $g 1267913 $s 993116
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 161 $c 1 $d 92-99 $e 20161110 $i 1213-8118 $m Biomedical papers of the Medical Faculty of the University Palacký, Olomouc Czech Republic $n Biomed. Pap. Fac. Med. Palacký Univ. Olomouc Czech Repub. (Print) $x MED00012606
- LZP __
- $b NLK118 $a Pubmed-20171025