Decreased expression of glutathione S-transferase M1 in HPV16-transfected human cervical keratinocytes in culture

• Published in: Carcinogenesis (New York) 1999-04, Vol.20 (4), p.699-703
• Main Authors: Chen, Chu, Nirunsuksiri, Wilas
• Format: Article
• Language: English
• Subjects: 1-chloro-2; 4-dinitrobenzene; Biological and medical sciences; Carcinogenesis, carcinogens and anticarcinogens; Carcinogens, Environmental - pharmacokinetics; CDNB; Cells, Cultured; Cervix Uteri - cytology; Disease Susceptibility; Enzyme Induction; Female; GAPDH; Gene Expression Regulation; Gene Expression Regulation, Viral; glutathione S-transferase; Glutathione Transferase - biosynthesis; Glutathione Transferase - deficiency; Glutathione Transferase - genetics; glyceraldehyde-3-phosphate dehydrogenase; GST; HCK; HPV; human cervical keratinocyte; human papillomavirus; human papillomvirus 16; Humans; Isoenzymes - biosynthesis; Isoenzymes - deficiency; Isoenzymes - genetics; keratinocyte serum-free medium; Keratinocytes - enzymology; Keratinocytes - virology; KSFM; Male; Medical sciences; Oncogene Proteins, Viral - genetics; Oncogene Proteins, Viral - physiology; Papillomavirus E7 Proteins; PBS; PCR; Penis - cytology; phosphate-buffered saline; polymerase chain reaction; Repressor Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - biosynthesis; RT–PCR; SDS; sodium chloride–sodium citrate buffer; sodium dodecyl sulfate; SSC; Stilbenes - metabolism; trans-stilbene oxide; Transfection; TSO; Tumors; Viruses
• ISSN: 0143-3334; 1460-2180
• DOI: 10.1093/carcin/20.4.699

Glutathione S-transferase (GST) M1 is a member of the GST μ family of cytosolic enzymes that have been hypothesized to catalyze the conjugation of glutathione to a large number of hydrophobic substances, including carcinogens such as polynuclear aromatic hydrocarbons present in tobacco smoke, leading to their excretion. Epidemiologic and experimental evidence suggests that the risk of cervical cancer is related to both human papillomavirus (HPV) infection and cigarette smoking. We compared the enzymatic activities and mRNA levels of GSTs in GSTM1-positive human cervical keratinocytes (HCKs) that had been transfected with HPV16 with those in the parental cells. The GSTM1 activity toward the substrate trans-stilbene oxide was 5- to 7-fold lower than in the parental cells. The relative mRNA level in HCK transfected with HPV16 E6/E7, as quantified by reverse transcriptase–polymerase chain reaction (RT–PCR) with normalization against endogenous glyceraldehyde-3-phosphate dehydrogenase (GAPDH) expression, was 6% that of the parental cells. It was 16 and 82%, respectively, in cells that were transfected with HPV16 E6 alone or HPV16 E7 alone. When quantified by competitive RT–PCR using an exogenous nuclease-resistant synthetic cyclophilin RNA transcript as control, the mRNA level in HCK transfected with HPV16 E6 was ~10-fold lower that that in the parental cells. It was ~5- to 7-fold lower in the HPV16 E7 or HPV16 E6/E7 cells. Our results suggest that viral infections, through the modulation of cellular xenobiotic-metabolizing enzymes, may play a role in the ability of cells to handle environmental carcinogens.