Abstract
Objective: To detect genetic alterations in nasopharyngeal carcinoma (NPC) in Cantonese, the population with the highest incidence of NPC, and to correlate the findings with clinical staging. Methods: Comparative genomic hybridization (CGH) was performed on 35 primary nasopharyngeal carcinomas and a nonparametric x2 test was used to analyze relationship between chromosome changes and clinical staging. Results: The identified common chromosomal alterations in NPC included gain of chromosomes 12q (21 cases, 60%), 4q (19cases, 43%), 3q (18 cases, 51%), 1q (15 cases, 43%),8q (14 cases, 40%), and 2q (12 cases, 30%). The most frequently detected loss of chromosomal materials involved chromosome 1p (24 cases, 69%), chromosome 3p (21 cases, 60%), 11q (20 cases, 57%), 14q (18 cases, 51%), 16q (14 cases, 40%), 13(12 cases, 34%), and 9p(11 cases, 31%). The high frequency (>50%) 4q gain and 1p loss were novel findings. Compared by nonparametric x2 test, gains on 12q and 8q were found mainly in stages III/IV and there were significant differences between two clinical stage groups (stages I/II vs stages III/IV). Conclusions: Current analysis has revealed a comprehensive profile of the chromosomal regions showing DNA copy number changes, which may harbor oncogenes or tumor suppressor genes involved in the development of primary NPC.
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Foundation item: This work was supported by the “973” National Key Basic Research Program of China (No.G1998051202) and the National Scientific Research Foundation for Excellent Young Scientist of China(type B) (No. 39825511).
Biography: Yan Jian,(1962–), doctor of medicine, attending physician, works at Cancer Center, Sun Yat-sen University of Medical Sciences, majors in oncology.
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Yan, J., Fang, Y., Liang, Q. et al. DNA copy profile in nasopharyngeal carcinoma and its correlation with clinical staging. Chin. J. Cancer Res. 13, 276–279 (2001). https://doi.org/10.1007/s11670-001-0047-3
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DOI: https://doi.org/10.1007/s11670-001-0047-3