CD30 is a survival factor and a biomarker for transformed human pluripotent stem cells

被引:115
作者
Herszfeld, D
Wolvetang, E
Langton-Bunker, E
Chung, TL
Filipczyk, AA
Houssami, S
Jamshidi, P
Koh, K
Laslett, AL
Michalska, A
Nguyen, L
Reubinoff, BE
Tellis, I
Auerbach, JM
Ording, CJ
Looijenga, LHJ
Pera, MF
机构
[1] Monash Univ, Med Res Inst, Clayton, Vic 3800, Australia
[2] Australian Stem Cell Ctr, Clayton, Vic 3800, Australia
[3] Amer Type Culture Collect, Stem Cell Ctr, Manassas, VA 20110 USA
[4] Erasmus Univ, Med Ctr, Dr Daniel Den Hoed Canc Ctr, Josephine Nefkens Inst,Lab Exp Patho Oncol, NL-3000 DR Rotterdam, Netherlands
关键词
D O I
10.1038/nbt1197
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The application of human embryonic stem (hES) cells in regenerative medicine will require rigorous quality control measures to ensure the safety of hES cell-derived grafts. During propagation in vitro, hES cells can acquire cytogenetic abnormalities(1-3) as well as submicroscopic genetic lesions, such as small amplifications or deletions(4). Many of the genetic abnormalities that arise in hES cell cultures are also implicated in human cancer development. The causes of genetic instability of hES cells in culture are poorly understood, and commonly used cytogenetic methods for detection of abnormal cells are capable only of low-throughput analysis on small numbers of cells. The identification of biomarkers of genetic instability in hES cells would greatly facilitate the development of culture methods that preserve genomic integrity. Here we show that CD30, a member of the tumor necrosis factor receptor superfamily, is expressed on transformed but not normal hES cells, and that CD30 expression protects hES cells against apoptosis.
引用
收藏
页码:351 / 357
页数:7
相关论文
共 30 条
  • [1] Impaired negative selection of T cells in Hodgkin's disease antigen CD30-deficient mice
    Amakawa, R
    Hakem, A
    Kundig, TM
    Matsuyama, T
    Simard, JJL
    Timms, E
    Wakeham, A
    Mittruecker, HW
    Griesser, H
    Takimoto, H
    Schmits, R
    Shahinian, A
    Ohashi, PS
    Penninger, JM
    Mak, TW
    [J]. CELL, 1996, 84 (04) : 551 - 562
  • [2] Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture
    Amit, M
    Carpenter, MK
    Inokuma, MS
    Chiu, CP
    Harris, CP
    Waknitz, MA
    Itskovitz-Eldor, J
    Thomson, JA
    [J]. DEVELOPMENTAL BIOLOGY, 2000, 227 (02) : 271 - 278
  • [3] Andrews PW, 2005, NAT BIOTECHNOL, V23, P795, DOI 10.1038/nbt0705-798
  • [4] Karyotype of human ES cells during extended culture
    Buzzard, JJ
    Gough, NM
    Crook, JM
    Colman, A
    [J]. NATURE BIOTECHNOLOGY, 2004, 22 (04) : 381 - 382
  • [5] Cowan CA, 2004, NEW ENGL J MED, V350, P1353, DOI 10.1056/NEJMsr040330
  • [6] Involvement of Sp1 and microsatellite repressor sequences in the transcriptional control of the human CD30 gene
    Croager, EJ
    Gout, AM
    Abraham, LJ
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (05) : 1723 - 1731
  • [7] Development of potent monoclonal antibody auristatin conjugates for cancer therapy
    Doronina, SO
    Toki, BE
    Torgov, MY
    Mendelsohn, BA
    Cerveny, CG
    Chace, DF
    DeBlanc, RL
    Gearing, RP
    Bovee, TD
    Siegall, CB
    Francisco, JA
    Wahl, AF
    Meyer, DL
    Senter, PD
    [J]. NATURE BIOTECHNOLOGY, 2003, 21 (07) : 778 - 784
  • [8] Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells
    Draper, JS
    Smith, K
    Gokhale, P
    Moore, HD
    Maltby, E
    Johnson, J
    Meisner, L
    Zwaka, TP
    Thomson, JA
    Andrews, PW
    [J]. NATURE BIOTECHNOLOGY, 2004, 22 (01) : 53 - 54
  • [9] Dürkop H, 2000, J PATHOL, V190, P613
  • [10] MOLECULAR-CLONING AND EXPRESSION OF A NEW MEMBER OF THE NERVE GROWTH-FACTOR RECEPTOR FAMILY THAT IS CHARACTERISTIC FOR HODGKINS-DISEASE
    DURKOP, H
    LATZA, U
    HUMMEL, M
    EITELBACH, F
    SEED, B
    STEIN, H
    [J]. CELL, 1992, 68 (03) : 421 - 427