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Demonstration of apoptosis in neuroblastoma and its relationship to tumour regression

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Abstract

The in vivo occurrence of apoptosis in neuroblastomas was investigated. Histologically, a number of tumour cells showed typical apoptotic changes, including cell shrinkage, condensed and fragmented nuclei, eosinophilic cytoplasm, and absence of the inflammatory response. These cells coincided closely with the so-called karyorrhectic cells. An electrophoretic DNA ladder, a functional hallmark of apoptosis, was demonstrated in four of six tumours, and DNA fragmentation was detected in situ by terminal deoxytransferase-mediated nick end-labelling in 26 of 35 tumour specimens (74%). The labelled cell counts ranged from 5 to 62 per 5000 tumour cells (mean±SD: 15.0±14.5). Immunoperoxidase staining revealed that an apoptosis-suppressing protein, bcl-2, was expressed abundantly in advanced-stage tumours, whereas it was absent from karyorrhectic-apoptotic cells. Several tumours with the potential for spontaneous regression were bcl-2-deficient. Immunostaining of the Fas receptor for apoptosis demonstrated that the tumour cells expressed this molecule on their cell surfaces. Our results provide evidence of apoptosis in neuroblastomas and suggest that bcl-2 and the Fas receptor may play a role in its regulatory mechanisms.

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Authors and Affiliations

  1. The Second Department of Pathology, St. Marianna University School of Medicine, Miyamae-ku, 216, Kawasaki, Japan

    H. Koizumi, T. Takakuwa & T. Uchikoshi

  2. The Third Department of Surgery, St. Marianna University School of Medicine, Miyamae-ku, 216, Kawasaki, Japan

    M. Wakisaka, K. Nakada, T. Fujioka & N. Yamate

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  1. H. Koizumi
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  2. T. Takakuwa
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  3. T. Uchikoshi
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  4. M. Wakisaka
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  5. K. Nakada
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  6. T. Fujioka
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  7. N. Yamate
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Koizumi, H., Takakuwa, T., Uchikoshi, T. et al. Demonstration of apoptosis in neuroblastoma and its relationship to tumour regression. Vichows Archiv A Pathol Anat 427, 167–173 (1995). https://doi.org/10.1007/BF00196522

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  • DOI: https://doi.org/10.1007/BF00196522

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