Fujii Hiroko, Amano Osamu, Kochi Mutsuyuki, Sakagami Hiroshi
Department of Oral Anatomy II, Meikai University School of Dentistry, Sakado Saitama, 350-0283, Japan.
Anticancer Res. 2003 Mar-Apr;23(2B):1353-6.
Previous studies have demonstrated the dramatic antitumor activity of sodium 5,6-benzylidene-L-ascorbate (SBA). However, the molecular mechanism of this antitumor action is unclear. We investigated the changes in the fine structures of a human submandibular gland carcinoma cell line, HSG, during the cell death induced by SBA. When HSG cells were incubated for 6 hours with non-cytotoxic concentrations of SBA, changes in the mitochondria, such as the disassembly of cristae and decrease in the electron density, were discrenible. At cytotoxic concentrations, the swelling and vacuolization of the mitochondria became apparent, while the nuclear architecture including the profile and ratio of heterochromatin and euchromatin and thickness of the nuclear membrane were intact. These data suggest that the mitochondria, not the nucleus, may be the target organelle of SBA, and support the ability of SBA to induce non-apoptotic cell death in HSG cells.
先前的研究已证明5,6-亚苄基-L-抗坏血酸钠(SBA)具有显著的抗肿瘤活性。然而,这种抗肿瘤作用的分子机制尚不清楚。我们研究了人下颌下腺癌细胞系HSG在SBA诱导的细胞死亡过程中精细结构的变化。当HSG细胞在无细胞毒性浓度的SBA中孵育6小时时,可观察到线粒体的变化,如嵴的解体和电子密度的降低。在细胞毒性浓度下,线粒体的肿胀和空泡化变得明显,而包括异染色质和常染色质的轮廓、比例以及核膜厚度在内的核结构保持完整。这些数据表明,线粒体而非细胞核可能是SBA的靶细胞器,并支持SBA诱导HSG细胞发生非凋亡性细胞死亡的能力。