Tsubaki Masanobu, Ogawa Naoki, Takeda Tomoya, Sakamoto Kotaro, Shimaoka Hirotaka, Fujita Arisa, Itoh Tatsuki, Imano Motohiro, Satou Takao, Nishida Shozo
Division of Pharmacotherapy, Kinki University School of Pharmacy, Kowakae, Higashi-Osaka, Japan.
Division of Pharmacotherapy, Kinki University School of Pharmacy, Kowakae, Higashi-Osaka, Japan; Department of Pharmacy, Sakai City Hospital, Sakai, Osaka, Japan.
Biomed Pharmacother. 2014 Oct;68(8):999-1005. doi: 10.1016/j.biopha.2014.09.009. Epub 2014 Sep 29.
Dimethyl fumarate (DMF) is a fumaric acid ester that is used to treat psoriasis and multiple sclerosis. Recently, DMF was found to exhibit anti-tumor effects. However, the molecular mechanisms underlying these effects have not been elucidated. In this study, we investigated the mechanism of DMF-induced apoptosis in different human hematopoietic tumor cell lines. We found that DMF induced apoptosis in different human hematopoietic tumor cell lines but it did not affect the normal human B lymphocyte cell line RPMI 1788. We also observed a concurrent increase in caspase-3 activity and in the number of Annexin-V-positive cells. Furthermore, an examination of the survival signals, which are activated by apoptotic stimuli, revealed that DMF significantly inhibited nuclear factor-κB (NF-κB) p65 nuclear translocation. In addition, DMF suppressed B-cell lymphoma extra-large (Bcl-xL) and X-linked inhibitor of apoptosis (XIAP) expression whereas Bcl-2, survivin, Bcl-2-associated X protein (Bax), and Bim levels did not change. These results indicated that DMF induced apoptosis by suppressing NF-κB activation, and Bcl-xL and XIAP expression. These findings suggested that DMF might have potential as an anticancer agent that could be used in combination therapy with other anticancer drugs for the treatment of human hematopoietic tumors.
富马酸二甲酯(DMF)是一种富马酸酯,用于治疗银屑病和多发性硬化症。最近,发现DMF具有抗肿瘤作用。然而,这些作用背后的分子机制尚未阐明。在本研究中,我们调查了DMF诱导不同人类造血肿瘤细胞系凋亡的机制。我们发现DMF诱导不同人类造血肿瘤细胞系凋亡,但不影响正常人类B淋巴细胞系RPMI 1788。我们还观察到caspase-3活性和膜联蛋白V阳性细胞数量同时增加。此外,对由凋亡刺激激活的存活信号的检查显示,DMF显著抑制核因子κB(NF-κB)p65核转位。此外,DMF抑制B细胞淋巴瘤-超大(Bcl-xL)和X连锁凋亡抑制蛋白(XIAP)表达,而Bcl-2、生存素、Bcl-2相关X蛋白(Bax)和Bim水平未改变。这些结果表明,DMF通过抑制NF-κB激活以及Bcl-xL和XIAP表达诱导凋亡。这些发现提示,DMF可能具有作为抗癌剂的潜力,可与其他抗癌药物联合用于治疗人类造血肿瘤。