From teratocarcinomas to embryonic stem cells

被引:192
作者
Andrews, PW [1 ]
机构
[1] Univ Sheffield, Dept Biomed Sci, Sheffield S10 2TN, S Yorkshire, England
关键词
embryonic stem cells; teratocarcinoma; embryonal carcinoma; human differentiation; plasticity;
D O I
10.1098/rstb.2002.1058
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The recent derivation of human embryonic stem (ES) cell lines, together with results suggesting an unexpected degree of plasticity in later, seemingly more restricted, stem cells (so-called adult stem cells), have combined to focus attention on new opportunities for regenerative medicine, as well as for understanding basic aspects of embryonic development and diseases such as cancer. Many of the ideas that are now discussed have a long history and much has been underpinned by the earlier studies of teratocarcinomas, and their embryonal carcinoma (EC) stem cells, which present a malignant surrogate for the normal stem cells of the early embryo. Nevertheless, although the potential of EC and ES cells to differentiate into a wide range of tissues is now well attested, little is understood of the key regulatory mechanisms that control their differentiation. Apart from the intrinsic biological interest in elucidating these mechanisms, a clear understanding of the molecular process involved will be essential if the clinical potential of these cells is to be realized. The recent observations of stem-cell plasticity suggest that perhaps our current concepts about the operation of cell regulatory pathways are inadequate, and that new approaches for analysing complex regulatory networks will be essential.
引用
收藏
页码:405 / 417
页数:13
相关论文
共 158 条
  • [1] Cell differentiation - Hepatocytes from nonhepatic adult stem cells
    Alison, MR
    Poulsom, R
    Jeffery, R
    Dhillon, AP
    Quaglia, A
    Jacob, J
    Novelli, M
    Prentice, G
    Williamson, J
    Wright, NA
    [J]. NATURE, 2000, 406 (6793) : 257 - 257
  • [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] CELL-SURFACE ANTIGENS OF A CLONAL HUMAN EMBRYONAL CARCINOMA CELL-LINE - MORPHOLOGICAL AND ANTIGENIC DIFFERENTIATION IN CULTURE
    ANDREWS, PW
    GOODFELLOW, PN
    SHEVINSKY, LH
    BRONSON, DL
    KNOWLES, BB
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1982, 29 (05) : 523 - 531
  • [5] ANDREWS PW, 1994, LAB INVEST, V71, P243
  • [6] A COMPARATIVE-STUDY OF 8 CELL-LINES DERIVED FROM HUMAN TESTICULAR TERATOCARCINOMA
    ANDREWS, PW
    BRONSON, DL
    BENHAM, F
    STRICKLAND, S
    KNOWLES, BB
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1980, 26 (03) : 269 - 280
  • [7] ANDREWS PW, 1984, LAB INVEST, V50, P147
  • [8] 3 MONOCLONAL-ANTIBODIES DEFINING DISTINCT DIFFERENTIATION ANTIGENS ASSOCIATED WITH DIFFERENT HIGH MOLECULAR-WEIGHT POLYPEPTIDES ON THE SURFACE OF HUMAN EMBRYONAL CARCINOMA-CELLS
    ANDREWS, PW
    BANTING, G
    DAMJANOV, I
    ARNAUD, D
    AVNER, P
    [J]. HYBRIDOMA, 1984, 3 (04): : 347 - 361
  • [9] DIFFERENT PATTERNS OF GLYCOLIPID ANTIGENS ARE EXPRESSED FOLLOWING DIFFERENTIATION OF TERA-2 HUMAN EMBRYONAL CARCINOMA-CELLS INDUCED BY RETINOIC ACID, HEXAMETHYLENE BISACETAMIDE (HMBA) OR BROMODEOXYURIDINE (BUDR)
    ANDREWS, PW
    NUDELMAN, E
    HAKOMORI, SI
    FENDERSON, BA
    [J]. DIFFERENTIATION, 1990, 43 (02) : 131 - 138
  • [10] Andrews PW, 1996, INT J CANCER, V66, P806, DOI 10.1002/(SICI)1097-0215(19960611)66:6<806::AID-IJC17>3.0.CO