Down-regulation of mitotic checkpoint in transformed human embryo lung fibroblasts induced by N-methyl-N'-nitro-N-nitrosoguaridine.
- Author:
Zong-chun YI
1
;
Min ZHANG
;
Juan-lin FU
;
Zhao WANG
;
Zong-can ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Cell Line, Transformed; Chromosome Aberrations; Down-Regulation; Fibroblasts; drug effects; Humans; Lung; cytology; Methylnitronitrosoguanidine; toxicity; Mitosis; drug effects; Mutation; Protein Kinases; genetics; Protein-Serine-Threonine Kinases
- From: Chinese Medical Journal 2004;117(7):1079-1083
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDMutations in mitotic checkpoint genes have been detected in several human cancers, which exhibit chromosome instability. We wanted to know whether mutation of hBub1 could occur in transformed human embryo lung fibroblasts (HELF) cells induced by a chemical carcinogen.
METHODSHELF cells were transformed by N-methyl-N'-nitro-N-nitrosoguaridine (MNNG), and three flasks of transformed HELF cells (named as T1, T2, and T3) were selected as amplifiers, and mutations of hBub1 in these transformed cells were analyzed by PCR-SSCP and sequencing.
RESULTSIt was found that any one of three transformed cell lines exhibited aneuploidy with a low mitotic checkpoint function. Subsequent PCR-SSCP and sequence analysis showed an AGT to CGT or ATT mutation at codon 80 in hBub1 gene in T1 cells with a resultant change in amino acid sequence.
CONCLUSIONOur study demonstrated that the mitotic checkpoint genes could be targets of MNNG.