Skip to main content
Log in

Immunohistochemical analysis of the p53 family members in human craniopharyngiomas

  • Original Article
  • Published:
Brain Tumor Pathology Aims and scope Submit manuscript

Abstract

Craniopharyngiomas are intracranial tumors that usually arise in the site around the sella turcica. They are composed of distinctive sheets of epithelial cells showing adamantinomatous or squamous-papillary histologic type. Because little is known about the tumorigenesis of cranio-pharyngiomas, we retrieved samples from 15 tumor cases to investigate the functional significance of the p53 family of transcription factors, which are known to be expressed in various human epithelia. Immunohistochemical analysis of these cases demonstrated similar expression profiles of p53 family members in the two histologic types of the tumor; i.e., strong nuclear expression of p63 was observed in all cell layers, and moderate to intense nuclear expression of p73 was observed in the basal cell layers. In contrast to p63 and p73, the reactivity of an archetypal tumor suppressor, p53, was occasional and weak in the two histologic types. Because p63 was widely expressed in the tumors, reverse transcription-polymerase chain reaction (RT-PCR) analysis was conducted to elucidate which spliced variant of p63 was expressed. The results showed that †Np63, lacking a terminal transactivation domain of p63, was the dominant isoform. Together with the reported evidence that the †Np63 isoform is highly expressed in human squamous-cell carcinomas, these data suggest that the cellular architecture characteristic of the expression of p53 family members may be required for the histogenesis of craniopharyngiomas, where †Np63 has a possible role in maintaining proliferative activity of the tumor cells, like squamous-cell carcinomas in other tissues.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Janzer RC, Burger PC, Giangaspero F, et al (2000) Craniopharyngioma. In: Kleihuse P, Cavenee WK (eds) Pathology and genetics, Tumor of the nervous system. IRAC, Lyon, pp 244–246

    Google Scholar 

  2. Xin W, Rubin MA, McKeever PE (2002) Differential expression of cytokeratins 8 and 20 distinguishes cranipharyngioma from Rathke cleft cyst. Arch Pathol Lab Med 126:1174–1178

    PubMed  CAS  Google Scholar 

  3. Sekine S, Shibata T, Kokubu A, et al (2002) Craniopharyngiomas of adamantinomatous type harbor beta-catenin gene mutations. Am J Pathol 161:1997–2001

    PubMed  CAS  Google Scholar 

  4. Lefranc F, Chevalier C, Vinchon M, et al (2003) Characterization of the levels of expression of retinoic acid receptors, galectin-3, macrophage migration inhibiting factor, and p53 in 51 adamantinomatous craniopharyngiomas. J Neurosurg 98:145–153

    Article  PubMed  CAS  Google Scholar 

  5. Rienstein S, Adams EF, Pilzer D, et al (2003) Comparative genomic hybridization analysis of craniopharyngiomas. J Neurosurg 98:162–164

    Article  PubMed  CAS  Google Scholar 

  6. Rickert CH, Paulus W, (2003) Lack of chromosomal imbalances in adamantinomatous and papillary craniopharyngiomas. J Neurol Neurosurg Psychiatry 74:260–261

    Article  PubMed  CAS  Google Scholar 

  7. Yang A, Kaghad M, Wang Y, et al (1998) p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol Cell 2:305–316

    Article  PubMed  CAS  Google Scholar 

  8. Kaghad M, Bonnet H, Yang A, et al (1997) Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers. Cell 90:809–819

    Article  PubMed  CAS  Google Scholar 

  9. Lee LA, Walsh P, Prater CA, et al (1999) Characterization of an autoantigen associated with chronic ulcerative stomatitis: the CUSP autoantigen is a member of the p53 family. J Invest Dermatol 113:146–151

    Article  PubMed  CAS  Google Scholar 

  10. De Laurenzi V, Rossi A, Terrinoni A, et al (2000) p63 and p73 transactivate differentiation gene promoters in human keratinocytes. Biochem Biophys Res Commun 273:342–346

    Article  PubMed  CAS  Google Scholar 

  11. Di Como CJ, Urist MJ, Babayan I, et al (2002) p63 expression profiles in human normal and tumor, tissues. Clin Cancer Res 8:494–501

    PubMed  Google Scholar 

  12. Ichimiya S, Kojima T, Momota H, et al (2002) p73 is expressed in human thymic epithelial cells. J Histochem Cytochem 50:455–462

    PubMed  CAS  Google Scholar 

  13. van Bokhoven H, Brunner HG (2002) Splitting p63. Am J Hum Genet 71:1–13

    Article  PubMed  Google Scholar 

  14. Yang A, Kaghad M, Caput D, et al (2002) On the shoulders of giants: p63, p73 and the rise of p53. Trends Genet 18:90–95

    Article  PubMed  Google Scholar 

  15. Benard J, Douc-Rasy S, Ahomadegbe JC (2003) TP53 family members and human cancers. Hum Mutat 21:182–191

    Article  PubMed  CAS  Google Scholar 

  16. Yang A, Kaghad M, Wang Y, et al (1998) p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol Cell 2:305–316

    Article  PubMed  CAS  Google Scholar 

  17. Yang A, Walker N, Bronson R, et al (2000) p73-deficient mice have neurological, pheromonal and inflammatory defects but lack spontaneous tumours. Nature 404:99–103

    Article  PubMed  CAS  Google Scholar 

  18. Pozniak CD, Radinovic S, Yang A, et al (2000) An anti-apoptotic role for the p53 family member, p73, during developmental neuron death. Science 289:304–306

    Article  PubMed  CAS  Google Scholar 

  19. Liefer KM, Koster MI, Wang XJ, et al (2000) Down-regulation of p63 is required for epidermal UV-B-induced apoptosis. Cancer Res 60:4016–4020

    PubMed  CAS  Google Scholar 

  20. Hu H, Xia SH, Li AD, et al (2002) Elevated, expression of p63 protein in human esophageal squamous cell carcinomas. Int J Cancer 102:580–583

    Article  PubMed  CAS  Google Scholar 

  21. Hibi K, Trink B, Patturajan M, et al (2000) AIS is an oncogene amplified in squamous cell carcinoma. Proc Natl Acad Sci USA 97:5462–5467

    Article  PubMed  CAS  Google Scholar 

  22. Suliman Y, Opitz OG, Avadhani A, et al (2001) p63 expression is associated with p53 loss in oral-esophageal epithelia of p53-deficient mice. Cancer Res 61:6467–6473

    PubMed  CAS  Google Scholar 

  23. Stiewe T, Putzer BM (2002) Role of p73 in malignancy: tumor suppressor or oncogene? Cell Death Differ 9:237–245

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hiroyuki Momota.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Momota, H., Ichimiya, S., Ikeda, T. et al. Immunohistochemical analysis of the p53 family members in human craniopharyngiomas. Brain Tumor Pathol 20, 73–77 (2003). https://doi.org/10.1007/BF02483450

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02483450

Key words

Navigation