Apoptosis: Molecular regulation of cell death and hematologic malignancies

被引:2
作者
Chiarugi, V [1 ]
Cinelli, M [1 ]
Magnelli, L [1 ]
Dello Sbarba, P [1 ]
机构
[1] Univ Florence, Dept Expt Pathol & Oncol, I-50134 Florence, Italy
关键词
apoptosis; hematologic malignancies;
D O I
10.1385/MB:20:3:305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe the molecular mechanisms of apoptosis and its relationships with hematologic malignancies, stressing the concept that, both positive and negative deregulation of apoptosis, may be involved in hematologic human diseases. So, this fundamental process must be balanced by so far unknown mechanisms, involving, caspases (cysteine proteases, cleaving the protein substrate after an aspartate residue). These, so far known, ten proteases, are interconnected in a molecular cascade, initiated by the release of cytochrome C from mitochondrial membranes and its interaction with APAF-1 (the homolog of the Caenorhabditis e. CED-4) and with caspase 9, that initiates the proteolitic cascade (1,2). The conclusion is that apoptosis is a very important process, but yet poorly known in molecular details, in spite of the efforts of many scientists. Even the role of bcl-2, the main gene protecting from apoptosis, is still unknown. We close this chapter with a list of ten different technical approaches that can be useful tools to study apoptosis, and tracing the molecular principles on which they are based.
引用
收藏
页码:305 / 314
页数:10
相关论文
共 51 条
  • [1] 2 SUBSETS OF HUMAN LYMPHOCYTES-T EXPRESSING GAMMA-ANTIGEN DELTA-ANTIGEN RECEPTOR ARE IDENTIFIABLE BY MONOCLONAL-ANTIBODIES DIRECTED TO 2 DISTINCT MOLECULAR-FORMS OF THE RECEPTOR
    BOTTINO, C
    TAMBUSSI, G
    FERRINI, S
    CICCONE, E
    VARESE, P
    MINGARI, MC
    MORETTA, L
    MORETTA, A
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (02) : 491 - 505
  • [2] Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development
    Cecconi, F
    Alvarez-Bolado, G
    Meyer, BI
    Roth, KA
    Gruss, P
    [J]. CELL, 1998, 94 (06) : 727 - 737
  • [3] PROTECTION FROM FAS-MEDIATED APOPTOSIS BY A SOLUBLE FORM OF THE FAS MOLECULE
    CHENG, JH
    ZHOU, T
    LIU, CD
    SHAPIRO, JP
    BRAUER, MJ
    KIEFER, MC
    BARR, PJ
    MOUNTZ, JD
    [J]. SCIENCE, 1994, 263 (5154) : 1759 - 1762
  • [4] Signal transduction by DR3, a death domain-containing receptor related to TNFR-1 and CD95
    Chinnaiyan, AM
    ORourke, K
    Yu, GL
    Lyons, RH
    Garg, M
    Duan, DR
    Xing, L
    Gentz, R
    Ni, J
    Dixit, VM
    [J]. SCIENCE, 1996, 274 (5289) : 990 - 992
  • [5] Chinnaiyan AM, 1996, J BIOL CHEM, V271, P4961
  • [6] CLONING AND STRUCTURAL-ANALYSIS OF CDNAS FOR BCL-2 AND A HYBRID BCL-2/IMMUNOGLOBULIN TRANSCRIPT RESULTING FROM THE T(14-18) TRANSLOCATION
    CLEARY, ML
    SMITH, SD
    SKLAR, J
    [J]. CELL, 1986, 47 (01) : 19 - 28
  • [7] COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
  • [8] COTTER TG, 1992, ANTICANCER RES, V12, P773
  • [9] THE ROLE OF APOPTOSIS IN ANTIBODY-DEPENDENT CELLULAR CYTOTOXICITY
    CURNOW, SJ
    GLENNIE, MJ
    STEVENSON, GT
    [J]. CANCER IMMUNOLOGY IMMUNOTHERAPY, 1993, 36 (03) : 149 - 155
  • [10] D'Mello SR, 1998, J NEUROCHEM, V70, P1809