PML down‐regulation in soft tissue sarcomas |
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Authors: | Bruno Vincenzi Giuseppe Perrone Daniele Santini Federica Grosso Marianna Silletta Annamaria Frezza Sabrina Rossi Antonio Russo Carla Rabitti Nicola Gebbia Giuseppe Badalamenti Paolo Casali Andrea Onetti Muda Angelo Paolo dei Tos Giuseppe Tonini |
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Institution: | 1. Department of Oncology, University Campus Bio‐Medico, Rome, Italy;2. Department of Surgical Pathology, University Campus Bio‐Medico, Rome, Italy;3. Department of Cancer Medicine, Istituto Nazionale dei Tumori, Milan, Italy;4. Department of Pathology, General Hospital, Treviso, Italy;5. Section of Medical Oncology, Department of Surgical and Oncological Sciences, University of Palermo, Palermo, Italy |
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Abstract: | To date, little is known concerning the promyelocytic leukemia gene (PML) status in tumors of different origin, and its expression has never been evaluated in soft tissue sarcoma. The aim of the present study is focused on the identification of differences in terms of PML protein expression between different types of soft tissue sarcoma and the corresponding normal surrounding tissue. PML protein expression has been assessed by immunohistochemistry in six different histologic types of soft tissue sarcoma (synovial sarcoma, myofibroblastic sarcoma, angiosarcoma, liposarcoma, pleomorphic sarcoma, and leiomyosarcoma) and in the corresponding normal surrounding tissue. PML resulted significantly down‐regulated in synovial sarcoma and in myofibroblastic sarcoma specimens. Also in angiosarcoma samples a significative difference in PML expression in comparison with normal specimens has been detected. Interestingly PML protein detection showed a different pattern of expression in the three liposarcoma histology types compared with corresponding nontumoral tissues. In particular PML protein resulted significantly down‐regulated in myxoid liposarcoma and in dedifferentiated liposarcoma. On the contrary no statistically significant difference was observed in pleomorphic liposarcoma compared to normal tissue specimens. Further investigations are needed to confirm these data and to assess the possible value of PML expression as a prognostic factor in these extremely aggressive diseases. J. Cell. Physiol. 224: 644–648, 2010. © 2010 Wiley‐Liss, Inc. |
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