J Appl Biomed 4:135-139, 2006 | DOI: 10.32725/jab.2006.014

Parthenolide has apoptotic and cytotoxic selective effect on B-chronic lymphocytic leukemia cells

Gustavo Horacio Marin, Eduardo Mansilla*
Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Argentina

B-chronic lymphocytic leukemia (B-CLL) is the most common form of leukemia in the western world. It results from a relentless accumulation of small mature monoclonal lymphocytes. Following a recent demonstration of a significant increase in the proliferative pool of CLL cells in vivo, the gradual accumulation of malignant B-CLL cells seems to be primarily the consequence of their selective survival advantages relative to their normal B-cell counterparts. As the disease is mainly caused by defective apoptosis it is thus a good candidate for treatment by proapoptotic agents. Even though a large amount of research has been done during the last past years, the prognosis has not changed. Because of this, new therapeutic strategies are urgently needed, especially those that could switch on new apoptotic responses. In order to test the ability of parthenolide, a sesquiterpene lactone, to induce apoptosis and cytotoxicity of B-CLL cells in vitro, we cultured these cells in the presence of this substance. Incubations were continued for 3 days. Samples of cells were taken from cultures at 0, 24, 48 and 72 hours to measure apoptosis and cell viability. Peripheral Blood Mononuclear Cells (PBMCs) from five normal donors were submitted to the same techniques and served as control samples. In this study we show for the first time that parthenolide has a potent apoptotic and cytotoxic effect on B-CLL. It is noteworthy that this substance has almost no impact on normal PBMCs. This evidence suggests that parthenolide might be a promising therapy for B-CLL.

Keywords: parthenolide; apoptosis; B-CLL

Received: January 12, 2006; Revised: March 14, 2006; Published: July 31, 2006  Show citation

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Marin GH, Mansilla E. Parthenolide has apoptotic and cytotoxic selective effect on B-chronic lymphocytic leukemia cells. J Appl Biomed. 2006;4(3):135-139. doi: 10.32725/jab.2006.014.
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