The inhibition of arylamine N-acetyltransferase (NAT) activity by ibuprofen was determined in a human colon tumour (adenocarcinoma) cell line. Two assay systems were employed, one with cellular cytosols (9000 g supernatant) and the other with intact colon tumour cell suspensions. The NAT activity in
Effects of aspirin on arylamine N-acetyltransferase activity and DNA adducts in human bladder tumour cells
โ Scribed by Chin-Chung Yeh; Jing-Gung Chung; Hsi-Chin Wu; Huei-Ling Chang; Feng-Tsgh Yeh; Chi-Fu Hung
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 55 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0260-437X
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โฆ Synopsis
Aspirin; N-acetyltransferase; 2-aminofluorene; DNA adduct; bladder cancer Aspirin (acetylsalicylic acid) was used to determine the inhibition of arylamine N-acetyltransferase (NAT) activity and DNA adduct formation in a human bladder tumour cell line (T24). The activity of NAT was measured by high-performance liquid chromatography, assaying for the amounts of N-acetyl-2-aminofluorene and N-acetyl-p-aminobenzoic acid and remaining 2-aminofluorene and p-aminobenzoic acid. Two assay systems were used: one with cytosol and the other with intact cells. High-performance liquid chromatography was also used to analyse for the 2-aminofluorene-DNA adducts. Intact bladder tumour cells were used. The results demonstrated that NAT activity and 2-aminofluorene-DNA adduct formation in human bladder tumour cells were inhibited by acetylsalicylic acid in a dose-dependent manner. The effects of acetylsalicylic acid on the values of the apparent K m and V max were also determined in both examined systems. The data also indicated that acetylsalicylic acid decreased the apparent values of K m and V max from human bladder tumour cells in both cytosol and intact cells.
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