Epithelioid sarcoma (ES) is a very aggressive soft-tissue tumor in vivo, but no experimental data on its invasive and metastatic behavior have been reported. In the present study, 3 different clonal sub-populations (GRU-1A, GRU-1B and GRU-1C), derived from the same human ES cell line, GRU-1, were in
Tumorigenicity of human lymphoblastoid cell lines, acquired during in vitro culture and associated with chromosome gains
โ Scribed by J. E. N. Morten; J. H. Hay; C. M. Steel; M. E. Foster; C. L. De; Angelis A. Busuttil
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- French
- Weight
- 835 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
Tumorigenicity of human lymphoma and lymphoblastoid &ell lines was assessed by their ability to form growing and transplantable masses on subcutaneous inoculation into neonatally thymectomized, Ara-C-protected, totalbody-irradiated mice. By these criteria, I 2 lines of known malignant origin were tumorigenic, I I lymphoblastoid lines, tested after less than one year of in vitro growth, were non-tumorigenic and 8/18 long-established lymphoblastoid lines produced transplantable tumours. All of the long-established lines had acquired karyotypic changes on prolonged culture, the predominant characteristic being a gain of whole chromosomes or of major chromosome segments. None showed the classical 8 I 4 translocation asrociated with Burkitt's lymphoma. Comparisons with nontumorigenic precursors (recovered from liquid nitrogen storage) and with other non-tumorigenic but chromoromally abnormal, lymphoblastoid lines suggest that imbalance of the dosage of genes carried on chromosomes 7.8 and 9 may be important in determining the tumorigenic phenotype.
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The human breast cell line HBLIOO acquires the capacity to invade normal tissues and to replace them by proliferation in vitro only at high passage levels (HPL). These cells therefore are a useful model for studying tumor progression in vitro. We have analyzed the expression of cell-surface markers