-
Something wrong with this record ?
Evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute lymphoblastic leukemia using biochip array technology
JM. Horacek, T. Kupsa, M. Vasatova, L. Jebavy, P. Zak,
Language English Country Ukraine
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Freely Accessible Science Journals
from 2006
ROAD: Directory of Open Access Scholarly Resources
from 2006
PubMed
24084464
Knihovny.cz E-resources
- MeSH
- Precursor Cell Lymphoblastic Leukemia-Lymphoma blood MeSH
- Protein Array Analysis methods MeSH
- Cytokines blood MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Cell Adhesion Molecules blood MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
AIM: Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with acute lymphoblastic leukemia (ALL) and in healthy subjects using biochip array technology. This approach allows multi-analytical determination from a single sample. METHODS: A total of 15 ALL patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by biochip based immunoassays on the Evidence Investigator analyzer. T-tests were used for statistical analysis. RESULTS: Comparing cytokine and adhesion molecule levels in ALL patients and in healthy subject, we found significant increase in serum VCAM-1 (p < 0.000001), ICAM-1 (p < 0.0001), L-selectin (p < 0.0001), IL-8 (p < 0.001), MCP-1 (p < 0.01), and significant decrease (p < 0.01) in serum IL-3 and IL-4. CONCLUSION: Our results indicate that serum levels of specific cytokines and adhesion molecules (VCAM-1, ICAM-1, L-selectin, IL-8, IL-3, IL-4, MCP-1) are significantly altered in patients with newly diagnosed ALL, reflecting acti-vity of the disease. Further investigation is needed to establish if these alterations could be used as a prognostic indicator for ALL.
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14050789
- 003
- CZ-PrNML
- 005
- 20140409123057.0
- 007
- ta
- 008
- 140401s2013 un f 000 0|eng||
- 009
- AR
- 035 __
- $a (PubMed)24084464
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a un
- 100 1_
- $a Horacek, J M
- 245 10
- $a Evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute lymphoblastic leukemia using biochip array technology / $c JM. Horacek, T. Kupsa, M. Vasatova, L. Jebavy, P. Zak,
- 520 9_
- $a AIM: Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with acute lymphoblastic leukemia (ALL) and in healthy subjects using biochip array technology. This approach allows multi-analytical determination from a single sample. METHODS: A total of 15 ALL patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by biochip based immunoassays on the Evidence Investigator analyzer. T-tests were used for statistical analysis. RESULTS: Comparing cytokine and adhesion molecule levels in ALL patients and in healthy subject, we found significant increase in serum VCAM-1 (p < 0.000001), ICAM-1 (p < 0.0001), L-selectin (p < 0.0001), IL-8 (p < 0.001), MCP-1 (p < 0.01), and significant decrease (p < 0.01) in serum IL-3 and IL-4. CONCLUSION: Our results indicate that serum levels of specific cytokines and adhesion molecules (VCAM-1, ICAM-1, L-selectin, IL-8, IL-3, IL-4, MCP-1) are significantly altered in patients with newly diagnosed ALL, reflecting acti-vity of the disease. Further investigation is needed to establish if these alterations could be used as a prognostic indicator for ALL.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a molekuly buněčné adheze $x krev $7 D015815
- 650 _2
- $a cytokiny $x krev $7 D016207
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a akutní lymfatická leukemie $x krev $7 D054198
- 650 _2
- $a čipová analýza proteinů $x metody $7 D040081
- 650 _2
- $a mladý dospělý $7 D055815
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kupsa, T $u -
- 700 1_
- $a Vasatova, M $u -
- 700 1_
- $a Jebavy, L $u -
- 700 1_
- $a Zak, P $u -
- 773 0_
- $w MED00174402 $t Experimental oncology $x 1812-9269 $g Roč. 35, č. 3 (2013), s. 229-30
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24084464 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20140401 $b ABA008
- 991 __
- $a 20140409123146 $b ABA008
- 999 __
- $a ok $b bmc $g 1017925 $s 849369
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 35 $c 3 $d 229-30 $i 1812-9269 $m Experimental oncology $n Exp Oncol $x MED00174402
- LZP __
- $a Pubmed-20140401