CGH analysis shows genetic similarities and differences in atypical fibroxanthoma and undifferentiated high grade pleomorphic sarcoma.

作者: Philipp U Heitz , Angela Baer , Bruno Paredes , Daniela Mihic-Probst , Paul Komminoth

DOI: 10.5167/UZH-111580

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摘要: Background: Atypical fibroxanthoma (AFX) and undifferentiated high grade pleomorphic sarcoma (UpS) are histologically very similar, if not identical. However, they differ significantly in clinical outcome. Materials Methods: We used comparative genomic hybridization (CGH) to screen 24 AFX 12 UpS for alterations. Results: DNA copy number changes were observed 20/24 all UpS. The most frequent alterations occurring with comparable frequency both tumors deletions on chromosomes 9p 13q. also detected statistically significant differences of genetic between the two concerning 1q, 3p, 5q, 11p, 11q, gains 7q, 12q level 5p 11q. Conclusion: Despite their similar histology, show clear This might contribute different biological behavior tumors. On other hand similarities 13q suggest a common pathogenetic pathway.

参考文章(26)
C. Doglioni, C. D. M. Fletcher, A. P. Dei Tos, D. Gasparotto, R. Maestro, L. Laurino, M. Boiocchi, Ultraviolet-induced p53 mutations in atypical fibroxanthoma. American Journal of Pathology. ,vol. 145, pp. 11- 17 ,(1994)
Clara Rizzardi, Francesca Angiero, Mauro Melato, Atypical fibroxanthoma and malignant fibrous histiocytoma of the skin. Anticancer Research. ,vol. 23, pp. 1847- 1851 ,(2003)
S. Asko-Seljavaara, M. Tarkkanen, S. Knuutila, M. Virolainen, M. L. Larramendy, T. Wiklund, C. Blomqvist, I. Elomaa, Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker. American Journal of Pathology. ,vol. 151, pp. 1153- 1161 ,(1997)
Jianming Zhao, Roland R. de Krijger, Dorette Meier, Ernst-Jan M. Speel, Parvin Saremaslani, Seraina Muletta-Feurer, Claudia Matter, Jürgen Roth, Philipp U. Heitz, Paul Komminoth, Genomic alterations in well-differentiated gastrointestinal and bronchial neuroendocrine tumors (carcinoids): marked differences indicating diversity in molecular pathogenesis. American Journal of Pathology. ,vol. 157, pp. 1431- 1438 ,(2000) , 10.1016/S0002-9440(10)64780-3
Alain Aurias, Xavier Sastre, Aline Mairal, Paul Fréneaux, Frédéric Chibon, Philippe Terrier, Jean-Michel Coindre, The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma. Cancer Research. ,vol. 60, pp. 6339- 6345 ,(2000)
Yoji Ariyama, Johji Inazawa, Tomoya Sakabe, Takashi Shinomiya, Tsutomu Fujiwara, Yoji Fukuda, Toshiki Mori, Yusuke Nakamura, Identification of a Novel Gene, MASL1 within an Amplicon at 8p23.1 Detected in Malignant Fibrous Histiocytomas by Comparative Genomic Hybridization Cancer Research. ,vol. 59, pp. 511- 515 ,(1999)
C. H. Cole, J. F. Magee, M. Gianoulis, P. C. J. Rogers, Malignant fibrous histiocytoma in childhood Cancer. ,vol. 71, pp. 4077- 4083 ,(1993) , 10.1002/1097-0142(19930615)71:12<4077::AID-CNCR2820711245>3.0.CO;2-6
Jonathan D. Oliner, Jennifer A. Pietenpol, Sam Thiagalingam, Jeno Gyuris, Kenneth W. Kinzler, Bert Vogelstein, Oncoprotein MDM2 conceals the activation domain of tumour suppressor p53 Nature. ,vol. 362, pp. 857- 860 ,(1993) , 10.1038/362857A0