Abstract
Deletions of the 3p arm have been detected in various solid tumors, but no study to date has investigated this deletion in diffuse large B-cell lymphoma (DLBCL). Recently, we demonstrated that 3p14.2 was deleted in approximately 30% of DLBCL cases by use of a genome-wide array-comparative genomic hybridization (CGH). For a more detailed examination of the genomic losses at 3p14.2, here we made use of contig BAC array for 3p14.2, and found that 12 DLBCL samples displayed losses. All of the deleted regions were located within the fragile histidine triad (FHIT) gene, and the most frequent region of loss was mapped to 0.4 Mbp of the region encompassing the introns 4 and 5 and exon 5 of the FHIT gene. Concomitant analysis of transcripts showed that the FHIT gene was aberrantly transcribed in 31% of the DLBCL samples examined and that the lost exons of the aberrant transcripts were correlated with genomic deletions. These findings indicate that (1) loss of genomic material at 3q14.2 is responsible for exon losses of the FHIT gene, and (2) genomic loss of the FHIT gene is one of the causes of the generation of aberrant transcripts.
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Acknowledgements
We are grateful to Drs Wen-Lin Kuo and Joe Gray at the University of California, San Francisco, for kindly providing us with a detailed protocol for array CGH. The outstanding technical assistance of Mss H Suzuki and Y Kasugai is also very much appreciated. This work was supported in part by a Grant-in-Aid for the Second-Term Comprehensive 10-year Strategy for Cancer Control from the Ministry of Health, Labor and Welfare, a Grant-in-aid for Science on Primary Areas (Cancer Research) from the Ministry of Education, Culture, Sports, Science and Technology and a Grant-in-Aid for Cancer Research from the Princess Takamatsu Cancer Research Fund.
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Kameoka, Y., Tagawa, H., Tsuzuki, S. et al. Contig array CGH at 3p14.2 points to the FRA3B/FHIT common fragile region as the target gene in diffuse large B-cell lymphoma. Oncogene 23, 9148–9154 (2004). https://doi.org/10.1038/sj.onc.1208136
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DOI: https://doi.org/10.1038/sj.onc.1208136
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