Volume 41, Issue 3 pp. 232-242
Research Article

Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissues

Thorgunnur Eyfjord Petursdottir

Thorgunnur Eyfjord Petursdottir

Department of Pathology, Landspitali University Hospital, Reykjavik, Iceland

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Unnur Thorsteinsdottir

Unnur Thorsteinsdottir

DeCode Genetics, Reykjavik, Iceland

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Jon Gunnlaugur Jonasson

Jon Gunnlaugur Jonasson

Department of Pathology, Landspitali University Hospital, Reykjavik, Iceland

Icelandic Cancer Registry, The Icelandic Cancer Society, Reykjavik, Iceland

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Pall Helgi Moller

Pall Helgi Moller

Department of Surgery, Landspitali University Hospital, Reykjavik, Iceland

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Chen Huiping

Chen Huiping

Institute for Experimental Pathology, University of Iceland at Keldur, Reykjavik, Iceland

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Johannes Bjornsson

Johannes Bjornsson

Department of Pathology, Landspitali University Hospital, Reykjavik, Iceland

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Valgardur Egilsson

Valgardur Egilsson

Department of Pathology, Landspitali University Hospital, Reykjavik, Iceland

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Stefan Imreh

Stefan Imreh

Microbiology and Tumor Biology Center (MTC), Karolinska Institutet, Stockholm, Sweden

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Sigurdur Ingvarsson

Corresponding Author

Sigurdur Ingvarsson

Institute for Experimental Pathology, University of Iceland at Keldur, Reykjavik, Iceland

Institute for Experimental Pathology, University of Iceland, Keldur v/Vesturlandsveg, 112 Reykjavik, IcelandSearch for more papers by this author
First published: 11 August 2004
Citations: 21

Abstract

A human chromosomal segment regularly lost during tumor formation of microcell hybrids in SCID mice has been mapped to 3p21.3. This segment, called chromosome 3 common eliminated region 1 (C3CER1, also referred to as CER1), may harbor multiple tumor-suppressor genes. Because it was found that similar regions were eliminated in an inter- and intraspecies system and in two tumor types (mouse fibrosarcoma and human renal cell carcinoma), we hypothesized that the importance of C3CER1 would transgress tissue specificity, that is, it could occur in tumors derived from multiple tissues. To evaluate the loss of C3CER1 in various human tumor types, we conducted loss of heterozygosity (LOH) analysis of 576 human solid tumors from 10 different tissues and compared the frequency of deletion in the C3CER1 area to that in two other regions on 3p: the FHIT/FRA3B region, at 3p14.2, and the VHL region, at 3p25.3. Deletions were detected in the C3CER1 region in 83% of informative tumors. Half (47%) the LOH-positive tumors showed LOH at all informative markers, indicating a large deletion. The other half (53%) had a discontinuous LOH pattern, suggesting interstitial deletions or breakpoints. The proportion of tumors with C3CER1 deletions was high in all tumor types investigated, ranging from 70% to 94%, except for the soft-tissue sarcomas (40%). In the VHL and FHIT regions, deletions were observed in 73% and 43%, respectively, of the tumors. Of the three 3p regions analyzed, the highest deletion frequency was observed in the C3CER1 region. Furthermore, we demonstrated that the interstitial deletions including C3CER1 prevail over 3p14.2–pter losses in solid tumors. © 2004 Wiley-Liss, Inc.

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