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维生素E琥珀酸酯是一种强效的新型抗肿瘤药物,在体内对肿瘤坏死因子相关凋亡诱导配体(Apo2配体)具有高选择性和协同性。

Vitamin E succinate is a potent novel antineoplastic agent with high selectivity and cooperativity with tumor necrosis factor-related apoptosis-inducing ligand (Apo2 ligand) in vivo.

作者信息

Weber Tobias, Lu Min, Andera Ladislav, Lahm Harald, Gellert Nina, Fariss Marc W, Korinek Vladimir, Sattler Wolfgang, Ucker David S, Terman Alexei, Schröder Andreas, Erl Wolfgang, Brunk Ulf T, Coffey Robert J, Weber Christian, Neuzil Jiri

机构信息

Institute for Prevention of Cardiovascular Diseases, Ludwig Maximilians University, Munich, 80336 Germany.

出版信息

Clin Cancer Res. 2002 Mar;8(3):863-9.

Abstract

Alpha-tocopheryl succinate (alpha-TOS), a redox-inactive analogue of vitamin E, is a strong inducer of apoptosis, whereas alpha-tocopherol (alpha-TOH) lacks apoptogenic activity (J. Neuzil et al., FASEB J., 15: 403-415, 2001). Here we investigated the possible antineoplastic activities of alpha-TOH and alpha-TOS and further explored the potential of alpha-TOS as an antitumor agent. Using nude mice with colon cancer xenografts, we found that alpha-TOH exerted modest antitumor activity and acted by inhibiting tumor cell proliferation. In contrast, alpha-TOS showed a more profound antitumor effect, at both the level of inhibition of proliferation and induction of tumor cell apoptosis. alpha-TOS was nontoxic to normal cells and tissues, triggered apoptosis in p53(-/-) and p21(Waf1/Cip1(-/-)) cancer cells, and exerted a cooperative proapoptotic activity with tumor necrosis factor-related apoptosis-inducing ligand (Apo2 ligand) due to differences in proapoptotic signaling. Finally, alpha-TOS cooperated with tumor necrosis factor-related apoptosis-inducing ligand in suppression of tumor growth in vivo. Vitamin E succinate is thus a potent and highly specific anticancer agent and/or adjuvant of considerable therapeutic potential.

摘要

α-生育酚琥珀酸酯(α-TOS)是维生素E的一种氧化还原惰性类似物,是一种强大的凋亡诱导剂,而α-生育酚(α-TOH)则缺乏凋亡诱导活性(J. Neuzil等人,《美国实验生物学会联合会杂志》,15: 403 - 415,2001年)。在此,我们研究了α-TOH和α-TOS可能的抗肿瘤活性,并进一步探索了α-TOS作为抗肿瘤药物的潜力。使用患有结肠癌异种移植瘤的裸鼠,我们发现α-TOH具有适度的抗肿瘤活性,其作用机制是抑制肿瘤细胞增殖。相比之下,α-TOS在抑制增殖和诱导肿瘤细胞凋亡水平上均显示出更显著的抗肿瘤效果。α-TOS对正常细胞和组织无毒,能诱导p53基因敲除和p21(Waf1/Cip1基因敲除)癌细胞凋亡,并且由于促凋亡信号的差异,与肿瘤坏死因子相关凋亡诱导配体(Apo2配体)发挥协同促凋亡活性。最后,α-TOS与肿瘤坏死因子相关凋亡诱导配体协同抑制体内肿瘤生长。因此,维生素E琥珀酸酯是一种具有强大且高度特异性的抗癌药物和/或具有相当治疗潜力的佐剂。

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