Smooth muscle actin expression in primary bone tumours

被引:0
作者
F. Hemingway
T. G. Kashima
G. Mahendra
A. Dhongre
P. C. W. Hogendoorn
F. Mertens
N. A. Athanasou
机构
[1] University of Oxford,Department of Pathology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences
[2] Leiden University Medical Centre,Department of Pathology
[3] Lund University,Department of Clinical Genetics, University and Regional Laboratories, Skane University Hospital
来源
Virchows Archiv | 2012年 / 460卷
关键词
Bone tumours; Alpha smooth muscle actin; Giant cells;
D O I
暂无
中图分类号
学科分类号
摘要
Alpha isoform of smooth muscle actin (SMA) expression has been reported in giant cell tumour of bone (GCTB) and other benign and malignant bone tumours, but the pattern of SMA expression and the precise nature of SMA-expressing cells in these lesions is uncertain. We determined by immunohistochemistry the expression of SMA and other muscle and vascular markers in normal bone, GCTB and a wide range of primary benign and malignant bone tumours. Cultured stromal cells of GCTB, chondroblastoma (CB), and aneurysmal bone cyst (ABC) were also analysed for SMA expression. SMA was only noted in blood vessels in normal bone. SMA was expressed by mononuclear stromal cells (MSC) cultured from GCTB, ABC and CB. SMA was strongly and diffusely expressed by MSC in non-ossifying fibroma, fibrous dysplasia, and “brown tumour” of hyperparathyroidism. SMA expression was also noted in GCTB, ABC, CB, chondromyxoid fibroma, malignant fibrous histiocytoma of bone and osteosarcoma. Little or no SMA was noted in Langerhans cell histiocytosis, simple bone cyst, Ewing’s sarcoma, osteoblastoma, osteoid osteoma, enchondroma, osteochondroma, chondrosarcoma, myeloma, lymphoma, chordoma and adamantinoma. Our findings show that there is differential SMA expression in primary bone tumours and that identifying the presence or absence of SMA is useful in the differential diagnosis of these lesions. The nature of SMA-expressing cells in bone tumours is uncertain but they are negative for desmin and caldesmon and could represent either myofibroblasts or perivascular cells, such as pericytes.
引用
收藏
页码:525 / 534
页数:9
相关论文
共 204 条
  • [1] Gunst SJ(2008)Actin cytoskeletal dynamics in smooth muscle: a new paradigm for the regulation of smooth muscle contraction Am J Physiol Cell Physiol 295 C576-C587
  • [2] Zhang W(1978)At least six different actins are expressed in a higher mammal: an analysis based on the amino acid sequence of the amino-terminal tryptic peptide J Mol Biol 126 783-802
  • [3] Vandekerckhove J(2006)Differential expression of smooth muscle myosin, smooth muscle actin, h-caldesmon, and calponin in the diagnosis of myofibroblastic and smooth muscle lesions of skin and soft tissue Am J Dermatopathol 28 105-111
  • [4] Weber K(2000)Is anti-h-caldesmon useful for distinguishing smooth muscle and myofibroblastic tumors? An immunohistochemical study Am J Clin Pathol 114 746-753
  • [5] Perez-Montiel MD(2009)Pericytes. Morphofunction, interactions and pathology in a quiescent and activated mesenchymal cell niche Histol Histopathol 24 909-969
  • [6] Plaza JA(2001)The myofibroblast: an assessment of controversial issues and a definition useful in diagnosis and research Ultrastruct Pathol 25 39-50
  • [7] Dominguez-Malagon H(1991)Immunophenotypic heterogeneity in osteosarcomas Hum Pathol 22 583-590
  • [8] Suster S(1997)Histological and immunohistochemical diversities, and proliferative activity and grading in osteosarcomas Cancer Detect Prev 21 280-287
  • [9] Ceballos KM(2007)Ezrin and alpha-smooth muscle actin are immunohistochemical prognostic markers in conventional osteosarcomas Virchows Arch 451 999-1007
  • [10] Nielsen GP(1997)Phalangeal intraosseous well-differentiated osteosarcoma of the hand Virchows Arch 430 185-189