Literature DB >> 12401825

Frequent expression of smooth muscle markers in malignant fibrous histiocytoma of bone.

T Ueda1, N Araki, M Mano, A Myoui, S Joyama, S Ishiguro, H Yamamura, K Takahashi, I Kudawara, H Yoshikawa.   

Abstract

BACKGROUND/AIMS: Malignant fibrous histiocytoma (MFH) of bone, a relatively rare primary malignant bone tumour, is a distinct clinicopathological entity as opposed to MFH derived from soft tissue. Although the true histogenesis of this condition is still controversial, a considerable number of cases of MFH in soft tissue show positive immunohistochemical reactivity for muscle markers such as desmin, common muscle actin (HHF35), and alpha smooth muscle actin (SMA), suggesting that MFH cells are myofibroblastic in nature.
METHODS: This study investigated immunoreactivity for several different muscle markers in 19 cases of MFH of bone together with reverse transcription polymerase chain reaction (RT-PCR) analysis on frozen tissue samples that were available in four cases, and compared the data with those found in 11 cases of osteosarcoma and 11 cases of soft tissue MFH treated over the same period.
RESULTS: Immunohistochemistry revealed that MFH of bone showed relatively frequent expression of smooth muscle markers, including calponin (nine cases), alpha-SMA (nine cases), and SM22alpha (18 cases), and this was confirmed by RT-PCR analysis. However, only one, two, and three cases of MFH of bone showed positive staining for desmin, MyoD1, and HHF35, respectively. Similarly, 11 osteosarcoma cases were relatively frequently positive for alpha-SMA (five cases), calponin (four cases), and SM22alpha (seven cases), and less frequently positive for desmin (one case), MyoD1 (none), and HHF35 (none). In contrast, very few MFH of soft tissue cases (n = 11) showed positive reactivity for all of these muscle markers. It has recently been reported that human bone marrow stromal cells also express various kinds of smooth muscle markers including alpha-SMA and calponin.
CONCLUSIONS: These results suggested that MFH of bone may derive from mesenchymal stromal cells in bone marrow and has a more myofibroblastic differentiation than soft tissue MFH.

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Year:  2002        PMID: 12401825      PMCID: PMC1769800          DOI: 10.1136/jcp.55.11.853

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  28 in total

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2.  Molecular cloning and sequence analysis of smooth muscle calponin.

Authors:  K Takahashi; B Nadal-Ginard
Journal:  J Biol Chem       Date:  1991-07-15       Impact factor: 5.157

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4.  Leiomyosarcomas and most malignant fibrous histiocytomas share very similar comparative genomic hybridization imbalances: an analysis of a series of 27 leiomyosarcomas.

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6.  Molecular cloning and characterization of human non-smooth muscle calponin.

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7.  Malignant fibrous histiocytoma of bone. The experience at the Rizzoli Institute: report of 90 cases.

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Journal:  Cancer       Date:  1984-07-01       Impact factor: 6.860

Review 8.  Primary leiomyosarcoma of bone: a clinicopathologic, immunohistochemical, and ultrastructural study of 33 patients and a literature review.

Authors:  C R Antonescu; R A Erlandson; A G Huvos
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9.  FU-3 monoclonal antibody: a specific marker for malignant fibrous histiocytoma? An analysis of 32 malignant soft tissue and bone sarcomas.

Authors:  M J Perez-Bacete; A Llombart-Bosch
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10.  Expression of the smooth muscle calponin gene in human osteosarcoma and its possible association with prognosis.

Authors:  H Yamamura; H Yoshikawa; M Tatsuta; H Akedo; K Takahashi
Journal:  Int J Cancer       Date:  1998-06-19       Impact factor: 7.396

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3.  Smooth muscle actin expression in primary bone tumours.

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4.  Expression of smooth muscle markers in so called malignant fibrous histiocytomas.

Authors:  T Hasegawa; F Hasegawa; T Hirose; T Sano; Y Matsuno
Journal:  J Clin Pathol       Date:  2003-09       Impact factor: 3.411

5.  Arousal of cancer-associated stroma: overexpression of palladin activates fibroblasts to promote tumor invasion.

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  5 in total

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