Testicular germ cell tumoun (TGCT) are cured in over 80% of patients by using combination chemotherapy. However, the mechanism regulating this sensitivity has not been defined. Because cells derived from patients with DNA repair syndromes are similar to TCGT in their sensitivity to certain DNA-damag
Hypersensitivity of human testis-tumour cell lines to chemotherapeutic drugs
✍ Scribed by John R. W. Masters; Edward J. Osborne; M. Claire Walker; Christopher N. Parris
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 670 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Metastatic testis tumours, in contrast to most other types of cancer, can be cured by drugs. To investigate which classes of chemotherapeutic drug are differentially toxic to testis‐tumour cells, we compared the in vitro dose‐response curves of 5 human testis and 5 bladder‐cancer cell lines to 12 compounds. The testis cells were hypersensitive to drugs that interact directly with DNA (m‐amsa, bleomycin, cisplatin, doxorubicin, methylni‐ trosourea, mitozolomide, etoposide, mitomycin‐C), but little or no difference between the 2 cell types was seen following exposure to drugs whose mechanisms of action do not involve direct interaction with DNA (methotrexate, 5‐fluorouracil, colchicine, vinblastine). We conclude that testis tumour cells are either less tolerant of, or have a reduced capacity to repair, DNA damage.
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