Angiopoietin-2 mRNA expression is increased in chronic lymphocytic leukemia patients with poor prognostic features
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- analýza přežití MeSH
- angiopoetin-2 krev genetika metabolismus MeSH
- antigeny CD38 krev metabolismus MeSH
- chronická lymfatická leukemie krev metabolismus patofyziologie MeSH
- dospělí MeSH
- exprese genu * MeSH
- geny pro těžké řetězce imunoglobulinů MeSH
- kohortové studie MeSH
- leukocyty mononukleární metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- membránové glykoproteiny krev metabolismus MeSH
- messenger RNA metabolismus MeSH
- nádorové biomarkery krev genetika metabolismus MeSH
- polymerázová řetězová reakce MeSH
- prognóza MeSH
- progrese nemoci MeSH
- senioři MeSH
- variabilní oblast imunoglobulinu genetika MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- angiopoetin-2 MeSH
- antigeny CD38 MeSH
- CD38 protein, human MeSH Prohlížeč
- membránové glykoproteiny MeSH
- messenger RNA MeSH
- nádorové biomarkery MeSH
- variabilní oblast imunoglobulinu MeSH
Several studies have demonstrated the potential prognostic importance of angiogenesis in chronic lymphocytic leukemia (CLL). Elevated expression of angiopoietin-2 (Ang-2), an angiogenic cytokine, was recently reported in CLL. However, data regarding prognostic significance of Ang-2 in CLL are limited. Therefore, we quantitated Ang-2 mRNA in purified mononuclear cells of 33 untreated CLL patients and compared the transcript levels to traditional as well as modern prognostic factors in patients with CLL (clinical stage, disease course, IgVH mutation status, CD38, and ZAP-70 expression). Elevated Ang-2 mRNA concentrations were detected in 12 cases; 21 patients had very low or undetectable levels of Ang-2 transcript. There was significant association between high Ang-2 mRNA levels and unmutated IgVH genes (n=27, P=0.010) and with CD38 expression (n=32, P=0.011), but not with ZAP-70 expression (n=32, P=0.784), Rai stage (n=33, P=0.305) or stable versus progressive clinical course (n=33, P=0.443). There was a trend towards shorter progression-free survival in patients with high Ang-2 expression; however, it did not reach statistical significance (P=0.090). Our pilot data show that Ang-2 mRNA is differentially expressed in patients with CLL and its increased expression appears to be associated with poor prognostic features. Further studies are needed to confirm the results in a larger patient cohort.
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