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Nuclear p63 expression in osteoblastic tumors

  • Michael E. Kallen
    ,
  • Melinda E. Sanders
    ,
  • Adriana L. Gonzalez
    ,
  • Jennifer O. Black
    ,
  • Vicki L. Keedy
    ,
  • Kenneth R. Hande
*Corresponding author for this work
  • Vanderbilt University
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Expression of the p63 tumor suppressor protein has been reported in the mononuclear stromal cells of giant cell tumor of the bone, which may represent osteoblast-precursor cells. Only a limited number of osteoblastic tumors have been studied for p63 expression thus far. We therefore examined whether p63 may serve as a marker for osteoblastic differentiation in osteosarcomas or as a differential diagnostic marker to distinguish osteoblastoma from osteosarcoma. Immunohistochemical stains for p63 were performed on a tissue microarray containing 71 chemotherapy naïve biopsy samples of osteosarcoma, 21 whole sections of osteosarcoma, and 8 osteoblastomas. Nuclear p63 was detected in seven of eight osteoblastomas but was restricted to stromal cells within primitive, immature-appearing areas of osteoid deposition. Although only 7 of 71 (10 %) biopsy samples of osteosarcoma represented on the tissue microarray were positive for p63, 7 of 21 (33 %) osteosarcomas were positive when whole tissue sections were evaluated. Although p63 is detected in most osteoblastomas, it is also observed in a significant subset of osteosarcomas, severely limiting its utility in distinguishing between benign and malignant osteoblastic tumors. The relatively low prevalence of p63 expression in osteosarcoma would also seem to preclude its use as a marker of osteoblastic differentiation in skeletal sarcomas.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1639-1644 (6 pages)

Journal (Volume, Issue Number)

Tumor Biology (Volume 33, Issue 5)

Publication milestones

  • Published - 10/2012

Publication status

Published - 10/2012

ISSN

1010-4283

Publication IDs

  • Scopus: 84868153096
  • PubMed: 22623071

Publication metrics

Metrics

Scopus
citations
SciVal
citations
4
SciVal
FWCI
0.29
SciVal
Author count
12
SciVal
Paper percentile
50
Fractional count
1
Fractional count
0.08
Fractional count
11
Fractional count
0.92
Fractional count
1
Fractional count
1

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Citation count
6
Captures
14