Mir S S, Richter B W, Duckett C S
Metabolism Branch, Division of Clinical Sciences, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Blood. 2000 Dec 15;96(13):4307-12.
CD30 is a member of the tumor necrosis factor (TNF) receptor superfamily that is expressed on activated lymphocytes, as well as on neoplastic cells of Hodgkin disease (HD) and anaplastic large cell lymphoma (ALCL). A number of reports have shown that, depending on cellular context, CD30 signaling can exert a variety of effects, ranging from cell death to cellular proliferation. In the present study this disparity was examined, using a number of ALCL- and HD-derived cell lines. Activation of CD30 led to the induction of apoptotic death of ALCL cells, along with the selective reduction of TNF receptor-associated factor 2 and impairment in the ability of these cells to activate the pro-survival transcription factor nuclear factor kappa B (NF-kappa B). In contrast, HD cells, which constitutively express NF-kappa B, were not susceptible to CD30-induced apoptosis but could be sensitized following ectopic overexpression of a superdominant I kappa B. These studies suggest that NF-kappa B plays a determining role in the sensitivity or resistance of lymphoma cells to CD30-induced apoptosis, which may have important consequences in the clinical treatment of CD30-positive neoplasia. (Blood. 2000;96:4307-4312)
CD30是肿瘤坏死因子(TNF)受体超家族的成员,在活化淋巴细胞以及霍奇金病(HD)和间变性大细胞淋巴瘤(ALCL)的肿瘤细胞上表达。许多报告表明,根据细胞环境的不同,CD30信号传导可产生多种效应,从细胞死亡到细胞增殖。在本研究中,使用多种源自ALCL和HD的细胞系对这种差异进行了研究。CD30的激活导致ALCL细胞凋亡死亡的诱导,同时TNF受体相关因子2选择性减少,并且这些细胞激活促生存转录因子核因子κB(NF-κB)的能力受损。相比之下,组成性表达NF-κB的HD细胞对CD30诱导的凋亡不敏感,但在超显性IκB异位过表达后可被致敏。这些研究表明,NF-κB在淋巴瘤细胞对CD30诱导的凋亡的敏感性或抗性中起决定性作用,这可能对CD30阳性肿瘤的临床治疗产生重要影响。(《血液》。2000年;96:4307 - 4312)