Human male germ cell tumor resistance to cisplatin is linked to TP53 gene mutation Journal Article


Authors: Houldsworth, J.; Xiao, H.; Murty, V. V. V. S.; Chen, W.; Ray, B.; Reuter, V. E.; Bosl, G. J.; Chaganti, R. S. K.
Article Title: Human male germ cell tumor resistance to cisplatin is linked to TP53 gene mutation
Abstract: Male germ cell tumors (GCTs) are uniquely sensitive to cisplatin-based chemotherapy, with more than 90% of newly diagnosed cases cured. The underlying cause for resistance to treatment in 20-30% of metastatic lesions remains to be identified. Unlike other solid tumors, no mutations in the TP53 gene have been identified to date in random panels of GCT specimens, which could account for the exquisite sensitivity of these tumors to genotoxic insult. However, in a panel of resistant GCTs that did either not respond to cisplatin-based chemotherapy or subsequently relapsed and resulted in the death of the patient, we have now identified a subset of tumors to contain TP53 mutations within exons 6-9. A cell line derived from one of these tumors (228A) displayed the same TP53 mutation as the tumor specimen, expressed only mutant TP53 mRNA, and exhibited a relative resistance to cisplatin in vitro in comparison to a cell line (218A) derived from a responsive tumor with wild-type TP53. The resistant cell line displayed a much reduced apoptotic cell death and did not exhibit an induction of transcription of the p53-responsive genes WAF1 and MDM2 following cisplatin treatment, compared to that observed in the sensitive cell line. The levels of bax, an agonist of apoptosis, were found to be reduced in the resistant cell line. The simplest explanation for the resistance of this subset of GCTs that are resistant to cisplatin-based chemotherapy, is the inability of the cells to mount an apoptotic response following exposure due to a functionally inactivating mutation in the TP53 gene.
Keywords: cancer chemotherapy; controlled study; gene mutation; human cell; mutation; cisplatin; antineoplastic agents; cell survival; apoptosis; gene expression; cancer cell culture; drug resistance; tumor cells, cultured; protein p53; oncogene; tumor suppressor gene; messenger rna; teratoma; neoplasms, germ cell and embryonal; gene induction; rhabdomyosarcoma; protein p21; germ cell tumor; spermatozoa; resistance; genes, p53; sequence analysis, dna; protein bax; tp53; polymorphism, single-stranded conformational; humans; human; male; priority journal; article
Journal Title: Oncogene
Volume: 16
Issue: 18
ISSN: 0950-9232
Publisher: Nature Publishing Group  
Date Published: 1998-05-07
Start Page: 2345
End Page: 2349
Language: English
PUBMED: 9620551
PROVIDER: scopus
DOI: 10.1038/sj.onc.1201770
DOI/URL:
Notes: Article -- Export Date: 12 December 2016 -- Source: Scopus
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MSK Authors
  1. Han Xiao
    59 Xiao
  2. Weiyi Chen
    20 Chen
  3. Victor Reuter
    1224 Reuter
  4. Raju S K Chaganti
    391 Chaganti
  5. George Bosl
    430 Bosl
  6. Vundavalli V. V. S. Murty
    53 Murty