The Microarray Expression Analysis Identifies BAX as a Mediator of β-Carotene Effects on Apoptosis
Authors:
Marek Bodzioch;
Aldona Dembinska-Kiec;
Jadwiga Hartwich;
Katarzyna Lapicka-Bodzioch;
Agnieszka Banas;
Anna Polus;
Joanna Grzybowska;
Iwona Wybranska;
Joanna Dulinska;
Dorota Gil;
Piotr Laidler;
Wojciech Placha;
Magdalena Zawada;
Agnieszka Balana-Nowak;
Tomasz Sacha;
Beata Kiec-Wilk;
Aleksander Skotnicki;
Christoph Moehle;
Thomas Langmann; Gerd Schmitz
DOI:
10.1207/s15327914nc5102_13
Publication Frequency:
6 issues per year
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Abstract
β-Carotene is a ubiquitous compound rich in foods. However, there are conflicting reports regarding its role in carcinogenesis. We performed a microarray expression analysis in normal [human umbilical vein endothelial cells (HUVECs)] and neoplastic (melanoma A375 and myelomonocytic leukemia U937) actively proliferating cells and found evidence that β-carotene stimulated vital cellular functions in the former and suppressed them in the latter. These differential effects correlated with the expression of the proapoptotic BCL2-associated X protein (BAX), which was downregulated in HUVECs and upregulated in the two neoplastic cell lines. The quantitative expression analysis using real-time polymerase chain reaction largely confirmed the inhibition of B-cell CLL/lymphoma 2 (BCL2) pathway-mediated apoptosis in HUVECs and its activation in melanoma and leukemic cells. The assays for apoptosis, detecting DNA breaks and caspase activation, showed consistent proapoptotic and antiapoptotic effects in U937 and HUVEC lines, respectively. However, β-carotene-induced expression changes of BAX and other BCL2 pathway genes did not lead to the predicted induction of apoptosis in the A375 cells.
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