[Establishment of transgenic cell line CHL-3A4 and its metabolic activation].

Article Details

Citation

Chen Q, Wu J, Yu Y

[Establishment of transgenic cell line CHL-3A4 and its metabolic activation].

Zhonghua Yu Fang Yi Xue Za Zhi. 1998 Sep;32(5):281-4.

PubMed ID
10322772 [ View in PubMed
]
Abstract

OBJECTIVE: To establish a model cell line CHL-3A4 to study metabolic pathways for some genotoxic chemicals. METHODS: Complimentary DNA (cDNA) of cloned cytochrome P450-3A4 gene in human liver tissue was transferred to Bluescript M13 vector with reverse transcription polymerase chain reaction (RT-PCR) and DNA recombinant techniques. Restriction endonuclease map analysis and sequencing of partial cloned fragment proved that CYP3A4 cDNA was cloned into Bluescript M13 vector. Then, recombinant expression plasmid pREP9-3A4 was constructed in eukaryotic cell and transfected into Chinese hamster CHL cells. RESULTS: It was proved that a CHL-3A4 transgenic cell line was established, which could lead metabolic activation for aflatoxin B1 (AFB1), sterigmatocystin (STC) and cyclophosphamide (CPA). CONCLUSION: The CHL-3A4 cell line established did express human cytochrome P450 3A4 and could lead metabolic activation for three genotoxic chemicals AFB1, STC and CPA.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Cytochrome P450 3A4P08684Details