Benzene increases aneuploidy in the lymphocytes of exposed workers: A comparison of data obtained by fluorescence in situ hybridization in interphase and metaphase cells

✍ Scribed by Luoping Zhang; Nathaniel Rothman; Yunxia Wang; Richard B. Hayes; Songnian Yin; Nina Titenko-Holland; Mustafa Dosemeci; Yao-Zhu Wang; Prema Kolachana; Wei Lu; Liqiang Xi; Gui-Lan Li; Martyn T. Smith

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 144 KB
• Volume: 34
• Category: Article
• ISSN: 0893-6692
• DOI: 10.1002/(sici)1098-2280(1999)34:4<260::aid-em6>3.0.co;2-p

✦ Synopsis

Benzene is an established human leukemogen that increases the level of chromosome aberrations in lymphocytes of exposed workers. Numerical aberrations (aneusomy) can be observed by fluorescence in situ hybridization (FISH) in both interphase and metaphase cells. Whereas interphase FISH allows nondividing cells to be analyzed, one advantage of metaphase FISH is that it can also detect structural changes. The present study compares the abilities of metaphase and interphase FISH to detect aneusomy of chromosomes 7 and 8 in healthy benzene-exposed human subjects. Metaphase and interphase cells from the peripheral blood of 43 workers exposed to benzene (median ϭ 31 ppm, 8-hr TWA) and 44 frequency-matched controls were analyzed by FISH. Normal diploid cells contained two hybridization signals, whereas those that were potentially monosomic contained one, trisomic 3 and tetrasomic 4. The frequency of cells with one hybridization signal for chromosome 7 in metaphase spreads rose from 2.72 Ϯ 0.19 (%, mean Ϯ SE) in controls to 3.79 Ϯ 0.63 in workers exposed to 31 or fewer ppm benzene and 5.9 Ϯ 0.85 in those exposed to more than 31 ppm (P trend Ͻ 0.0001). No similar dose-dependent increase in the frequency of cells with one hybridization signal was observed by interphase FISH, probably because of probe overlap artifact. Although significant dose-dependent increases in the frequency of cells with three hybridization signals for chromosome 7 were detected by both methods in the higher-exposed group, a larger, more significant difference was detected by metaphase FISH between controls and workers exposed to 31 or fewer ppm. Similar data were obtained for chromosome 8. Interphase and metaphase FISH were moderately correlated for three hybridization signals but not for one hybridization signal in chromosome 7 or 8. In general, metaphase FISH was more sensitive in detecting both monosomy and trisomy in the lymphocytes of exposed workers.