C. Keshava et al., Genomic instability in silica- and cadmium chloride-transformed BALB/c-3T3and tumor cell lines by random amplified polymorphic DNA analysis, MUT RES-F M, 425(1), 1999, pp. 117-123
Citations number
21
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
Our earlier studies using random amplified polymorphic DNA (RAPD) analysis
have shown genetic instability in human lung cancer tissues. Here we have i
nvestigated the potential for genetic instability in silica- and cadmium ch
loride (CdCl2)-transformed BALB/c-3T3 cell lines. Non-transformed, transfor
med BALB/c-3T3 cells, and tumor cell lines (obtained by injecting nude mice
with transformed cell lines) were analyzed for genomic changes, DNAs from
10 different transformed clones and their corresponding tumor cell lines we
re amplified individually by RAPD analysis using 10 arbitrary primers. DNA
from non-transformed BALB/c-3T3 cells was used as a control to compare gene
tic alterations, if any, between non-transformed, transformed and tumor cel
l populations. PCR products from RAPD were electrophoretically separated on
agarose gels and the banding profiles were visualized by ethidium bromide
staining. Five of the 10 primers tested revealed genomic changes in silica-
transformed cell Lines when compared to non-transformed BALB/c-3T3 cells. C
omparison of all 10 transformed and tumor cell lines showed varied degrees
of genomic changes using all 10 primers. CdCl2-transformed cell lines displ
ayed fewer genomic changes, only three of 10 primers showed a positive resu
lt. CdCl2-transformed cells and their corresponding tumor cell lines showed
specific banding pattern differences in six of the 10 samples tested with
six of the 10 primers. Changes in band intensity were the most commonly obs
erved changes both in silica- and CdCl2-transformed and tumor cell lines. T
he results seem to indicate a progressive change in genomic rearrangements
which may directly or indirectly be associated with progression of tumorige
nesis. (C) 1999 Elsevier Science B.V, All rights reserved.