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TRAIL/TRAILR系统与凋亡 被引量:3

The System of TRAIL/TRAILR and Apoptosis
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摘要 TRAIL是近年来发现的凋亡分子之一 ,其最显著的特征就是能够选择性的诱导肿瘤细胞或转化细胞的凋亡 ,而对正常组织没有明显的毒性作用。目前发现TRAIL分子在体内有 4个膜结合型受体 ,和一个分泌型受体。这些受体在体内不同组织的选择性表达参与调控不同组织对TRAIL诱导凋亡的敏感性。因此 ,本文从TRAIL和TRAILR的发现、分子结构、表达调控、和诱导凋亡的分子机制 4个方面详细介绍了TRAIL与凋亡的关系。
作者 刘书逊
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 2001年第3期227-230,共4页 Chinese Journal of Cancer Biotherapy
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  • 1[1]Wiley SR, Schooley K, Smolak PJ, et al. Identification and characterization of a new member of the TNF family that induces apoptosis[J]. Immunity, 1995, 3: 673-682.
  • 2[2]Pan G, O′Rourke K, Chinnaiyan AM, et al. The receptor for the cytotoxic ligand TRAIL[ J ]. Science, 1997, 276: 111-113.
  • 3[3]Screaton GR, Mongkolsapaya J, Xu XN, et al. TRICK2, a new alternatively spliced receptor that transduces the cytotoxic signal from TRAIL[J]. Curr Biol, 1997, 7: 693-696.
  • 4[4]Pan G, Ni J, Wei YF, et al. An antagonist decoy receptor and a death domain-containing receptor for TRAIL [ J ]. Science, 1997,277: 815-818.
  • 5[5]Mongkolsapaya J, Cowper AE, Xu XN, et al. Lymphocyte inhibitor of TRAIL (TNF-related apoptosis-inducing ligand): A new receptor protecting lymphocytes from the death ligand TRAIL [ J ]. J Immunol,1998, 160: 3-6.
  • 6[6]Pan G, Ni J, Yu G, et al. TRUNDD, a new member of the TRAIL receptor family that antagonizes TRAIL signalling [ J ]. FEBS Lett,1998, 424: 41-45.
  • 7[7]Emery JG, McDonnell P, Burke MB, et al. Osteoprotegerin is a receptor for the cytotoxic ligand TRAIL[ J]. J Biol Chem, 1998, 273:14363-14367.
  • 8[8]Gruss HJ. Molecular, structural, and biological characteristics of the tumor necrosis factor ligand superfamily [ J ]. Int J Clin Lab Res,1996, 26: 143-159.
  • 9[9]Sheridan JP, Marsters SA, Pitti RM, et al. Control of TRAIL-induced apoptosis by a family of signaling and decoy receptors [J]. Science,1997, 277: 818-821.
  • 10[10]Degli-Esposti MA, Smolak PJ, Walczak H, et al. Cloning and characterization of TRAIL-R3, a novel member of the emerging TRAIL receptor family[J]. J Exp Med, 1997, 186: 1165-1170.

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