کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1904718 1534654 2014 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The arachidonic acid–LTB4–BLT2 pathway enhances human B-CLL aggressiveness
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی سالمندی
پیش نمایش صفحه اول مقاله
The arachidonic acid–LTB4–BLT2 pathway enhances human B-CLL aggressiveness
چکیده انگلیسی


• B-CLL shows deregulation of the oxidative cascade of polyunsaturated fatty acids.
• Aggressive cells show enhanced expression of cPLA2alpha, iPLA2beta, 5LOX, and LTA4H.
• BLT2, rather than BLT1, plays a major role in B-CLL aggressiveness.

Deregulation of the oxidative cascade of poly-unsaturated fatty acids (PUFAs) has been associated with several cancers, including chronic lymphocytic leukemia (B-CLL). Leukotriene B4 (LTB4), a metabolite of arachidonic acid (AA), is produced by B-CLL and contributes to their survival. The aim of the present study was to analyze the activity of the oxidative cascade of PUFAs in B-CLL. Purified B cells from patients and normal B CD5 positive cells were subjected to flow cytometry, Western-blot and RT-qPCR analyses. LTB4 plasma and intracellular concentrations were determined by ELISA. Our results showed that aggressive B-CLL tumor cells, i.e. cells with an annual proliferation index above 2, over-expressed calcium-dependent and calcium-independent phospholipases A2 (cPLA2-alpha and iPLA2-beta, respectively), 5-lipoxygenase (5LOX) and leukotriene A4 hydroxylase (LTA4H). Intracellular LTB4 levels were lower in the most aggressive cells than in cells with a smaller proliferation index, despite equivalent plasma levels, and lower expression of cytochrome P450 4F3A (CYP4F3A), one major enzyme involved in LTB4 inactivation. Since BLT2, a LTB4 membrane receptor was also more often expressed on aggressive tumor cells, and since a BLT2 inhibitor significantly impaired B-CLL viability in vitro, we propose that LTB4 was efficiently trapped onto BLT2 present on aggressive tumors, thereby eliciting an autocrine response. Taken together our results demonstrate a major deregulation of the pathway leading to LTB4 synthesis and degradation in B-CLL cells, and provide a framework for understanding how these modifications promote cell survival and proliferation, especially in the most aggressive BCLL.

Legend: 5LOX: 5-lipoxygenase, LTA4H: leukotriene A4 hydrolase, AA: arachidonic acid, PL: membrane phospholipids, cPLA2: calcium-dependent phospholipase A2alpha, iPLA2: calcium-independent phospholipase A2beta.Figure optionsDownload high-quality image (184 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - Volume 1842, Issue 11, November 2014, Pages 2096–2105
نویسندگان
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