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Journal articles on the topic 'Methylcholanthrene'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 August 2024

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1

Arnold, P. S., R. C. Garner, and B. Tierney. "Purification and photoaffinity labelling of a rat cytosolic binding protein specific for 3-methylcholanthrene." Biochemical Journal 242, no. 2 (1987): 375–81. http://dx.doi.org/10.1042/bj2420375.

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Rat hepatic cytosolic proteins which sediment at 4-5 S on sucrose gradients exhibit high-affinity saturable binding for the carcinogen 3-methylcholanthrene. A rat liver protein of Stokes' radius 3 nm, Mr by sodium dodecyl sulphate/polyacrylamide-gel electrophoresis of 39,000 and with specific 3-methylcholanthrene-binding activity sedimenting at 4.5 S, has been purified 315-fold to apparent homogeneity by using affinity chromatography on a column of 1-hydroxy-3-methylcholanthrene coupled to epoxy-activated Sepharose 6B, in conjunction with two gel-filtration steps. The protein purified by this

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2

Jacobs, J. M., P. R. Sinclair, W. J. Bement, R. W. Lambrecht, J. F. Sinclair, and J. A. Goldstein. "Oxidation of uroporphyrinogen by methylcholanthrene-induced cytochrome P-450. Essential role of cytochrome P-450d." Biochemical Journal 258, no. 1 (1989): 247–53. http://dx.doi.org/10.1042/bj2580247.

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We have previously shown that uroporphyrinogen is oxidized to uroporphyrin by microsomes (microsomal fractions) from 3-methylcholanthrene-pretreated chick embryo liver [Sinclair, Lambrecht & Sinclair (1987) Biochem. Biophys. Res. Commun. 146, 1324-1329]. We report here that a specific antibody to chick liver methylcholanthrene-induced cytochrome P-450 (P-450) inhibited both uroporphyrinogen oxidation and ethoxyresorufin O-de-ethylation in chick-embryo liver microsomes. 3-Methylcholanthrene-pretreatment of rats and mice markedly increased uroporphyrinogen oxidation in hepatic microsomes as

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3

Lambrecht, R. W., J. M. Jacobs, P. R. Sinclair, and J. F. Sinclair. "Inhibition of uroporphyrinogen decarboxylase activity. The role of cytochrome P-450-mediated uroporphyrinogen oxidation." Biochemical Journal 269, no. 2 (1990): 437–41. http://dx.doi.org/10.1042/bj2690437.

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It was previously shown that uroporphyrinogen oxidation is catalysed by a form of cytochrome P-450 induced by 3-methylcholanthrene [Sinclair, Lambrecht & Sinclair (1987) Biochem. Biophys. Res. Commun. 146, 1324-1329]. We have now measured uroporphyrinogen oxidation and uroporphyrinogen decarboxylation simultaneously in 10,000 g supernatants from the livers of methylcholanthrene-treated mice and chick embryos incubated with an NADPH-generating system. We found that uroporphyrinogen oxidation is associated with inhibition of uroporphyrinogen decarboxylase activity. The decreased uroporphyrin

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4

Song, B. J., H. V. Gelboin, S. S. Park, and F. K. Friedman. "Epitope-relatedness and phenotyping of hepatic cytochromes P-450 with monoclonal antibodies." Biochemical Journal 231, no. 3 (1985): 671–76. http://dx.doi.org/10.1042/bj2310671.

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The epitope-specific cytochrome P-450 content of animal livers was analysed by radioimmunoassay using a panel of seven monoclonal antibodies (MAbs) made to a 3-methylcholanthrene-induced rat liver cytochrome P-450. Competitive radioimmunoassays utilizing a reference radiolabelled MAb and a series of unlabelled MAbs indicated that there are at least three distinct classes of MAbs to different epitopes on cytochrome P-450. In addition, a direct radioimmunoassay employing a radiolabelled second antibody detected MAb-specific cytochromes P-450 in livers from different animals. This radioimmunoassa

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5

Seidel, S. L., and T. K. Shires. "Purification and characterization of a previously unreported form of cytochrome P-448 from the liver of 3-methylcholanthrene-pretreated rats." Biochemical Journal 235, no. 3 (1986): 859–68. http://dx.doi.org/10.1042/bj2350859.

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At least four hepatic isoenzymes of cytochrome P-450 were purified and characterized from rats treated with 3-methylcholanthrene. A monoclonal antibody developed against one of the forms (designated cytochrome P-450 MC-B) and polyclonal antibodies against others were used to demonstrate that form MC-B is immunologically distinct from other methylcholanthrene-inducible forms. Limited N-terminal amino acid sequencing showed that cytochrome P-450 MC-B has a primary structure that differs from the N-terminal sequences of other established rat isoenzymes. Cytochrome P-450 MC-B has a minimum Mr of 5

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6

Sinclair, P., J. Frezza, J. Sinclair, et al. "Immunochemical detection of different isoenzymes of cytochrome P-450 induced in chick hepatocyte cultures." Biochemical Journal 258, no. 1 (1989): 237–45. http://dx.doi.org/10.1042/bj2580237.

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This study investigated whether the same cytochrome P-450 (P-450) isoenzymes were inducible in cultures of chick-embryo hepatocytes as in the liver of chicken embryos. We purified two isoenzymes of cytochrome P-450 from the livers of 17-day-old-chick embryos: one of molecular mass approx. 50 kDa induced in vivo by the phenobarbital-like inducer glutethimide, and the second of approx. 57 kDa induced by 3-methylcholanthrene. Rabbit antiserum against the 50 kDa protein inhibited benzphetamine demethylase activity in hepatic microsomes (microsomal fractions) from glutethimide-treated chick embryo.

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7

Lutz, Charles T., Garvan Browne, and C. Rosemarie Petzold. "Methylcholanthrene causes increased thymocyte apoptosis." Toxicology 128, no. 2 (1998): 151–67. http://dx.doi.org/10.1016/s0300-483x(98)00043-2.

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8

Harvey, Ronald G., and Cecilia Cortez. "Synthesis of cholanthrene and 6-methylcholanthrene, biologically active analogs of the potent carcinogen 3-methylcholanthrene." Journal of Organic Chemistry 52, no. 2 (1987): 283–84. http://dx.doi.org/10.1021/jo00378a025.

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9

Laizé, Vincent, Paulo J. Gavaia, Marco Tarasco, et al. "Osteotoxicity of 3-methylcholanthrene in fish." Ecotoxicology and Environmental Safety 161 (October 2018): 721–28. http://dx.doi.org/10.1016/j.ecoenv.2018.06.035.

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10

Sheen, Yhun Y., Sun S. Kim, and Hea C. Yun. "Effect of 3-methylcholanthrene on rat uterus: Uterine growth and mechanism of action of 3-methylcholanthrene." Archives of Pharmacal Research 16, no. 4 (1993): 276–82. http://dx.doi.org/10.1007/bf02977516.

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11

Ohnishi, Taira, Hirohito Yoneyama, Tatushichiro Hamamoto, Toshihiko Ishida, Jirou Takahara, and Yoshiyuki Ichikawa. "Induction of Cytochrome P-450-linked Monooxygenase System in Rat Liver Microsomes by Xiao-Chaihu-Tang." American Journal of Chinese Medicine 24, no. 02 (1996): 143–51. http://dx.doi.org/10.1142/s0192415x96000190.

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The administration of Xiao-Chaihu- Tang (TJ-9) for 2 weeks induced a 25% increase in the content of cytochrome P-450 in female rat liver microsomes, while the content in male rats remained unchanged. The enzymatic activities toward various xenobiotics were stimulated in female rats, the levels being in the range of 125-250% of those in the control rats. Among these xenobiotics, the metabolic rates for substrates of cytochrome P-450 2El were significantly enhanced in female rats. On the other hand, the activities toward various xenobiotics in male rats were unchanged. When 3-methylcholanthrene

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12

Lee, Hongmee, and Ronald G. Harvey. "SYNTHESES OF OXYGENATED DERIVATIVES OF 3-METHYLCHOLANTHRENE." Organic Preparations and Procedures International 20, no. 2 (1988): 123–28. http://dx.doi.org/10.1080/00304948809355799.

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13

N'Guyen, Quoc-Binh, Frederique Fallone, Eric Seree, et al. "Serum increases CYP1A1 induction by 3-methylcholanthrene." Biochemical and Biophysical Research Communications 297, no. 2 (2002): 249–54. http://dx.doi.org/10.1016/s0006-291x(02)02177-0.

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14

Gimisis, Thanasis, and Masato Koreeda. "A highly efficient synthesis of 3-methylcholanthrene." Journal of Organic Chemistry 58, no. 25 (1993): 7158–61. http://dx.doi.org/10.1021/jo00077a045.

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15

Ishizaka, S. T., and F. Lilly. "Genetically determined resistance to 3-methylcholanthrene-induced lymphoma is expressed at the level of bone marrow-derived cells." Journal of Experimental Medicine 166, no. 2 (1987): 565–70. http://dx.doi.org/10.1084/jem.166.2.565.

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Reciprocal bone marrow transfers were performed between mouse strains sensitive or resistant to 3-methylcholanthrene-induced thymic lymphoma. Sensitivity and resistance are properties inherent in bone marrow, and cannot be altered by maturation of marrow in an environment of the opposite phenotype.

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16

Flesher, James W., Jamie Horn, and Andreas F. Lehner. "Carcinogenicity of 1-Hydroxy-3-methylcholanthrene and Its Electrophilic Sulfate Ester 1-Sulfooxy-3-methylcholanthrene in Sprague-Dawley Rats." Biochemical and Biophysical Research Communications 243, no. 1 (1998): 30–35. http://dx.doi.org/10.1006/bbrc.1997.8048.

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17

Prasanna, P., M. M. Jacobs, and S. K. Yang. "Selenium inhibition of benzo[a]pyrene, 3-methylcholanthrene, and 3-methylcholanthrylene mutagenicity in Salmonella typhimurium strains TA98 and TA100." Mutation Research Letters 190, no. 2 (1987): 101–5. http://dx.doi.org/10.1016/0165-7992(87)90039-x.

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18

Johnson, Brian E., Robin G. Bell, and Rodney R. Dietert. "3-Methylcholanthrene-Induced Immunosuppression in Mice toTrichinella SpiralisAntigens." Immunopharmacology and Immunotoxicology 12, no. 2 (1990): 237–56. http://dx.doi.org/10.3109/08923979009019671.

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19

Myers, Steven R., Jerry W. Blake, and James W. Flesher. "Metabolism of 3-methylcholanthrene in rat liver cytosol." Chemico-Biological Interactions 71, no. 4 (1989): 393–401. http://dx.doi.org/10.1016/0009-2797(89)90113-0.

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20

Anderson, Lucy M., Ann B. Jones та Charles W. Riggs. "Long-Term (Imprinting) Effects of Transplacental Treatment of Mice with 3-Methylcholanthrene or β-Naphthoflavone on Hepatic Metabolism of 3-Methylcholanthrene". Pharmacology & Toxicology 69, № 3 (1991): 178–88. http://dx.doi.org/10.1111/j.1600-0773.1991.tb01294.x.

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21

Esmarch, Ole. "DEPOSITION OF METHYLCHOLANTHRENE IN SOME ORGANS OF THE RAT.*." Acta Pathologica Microbiologica Scandinavica 19, no. 1 (2009): 79–99. http://dx.doi.org/10.1111/j.1699-0463.1942.tb03336.x.

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22

Esmarch, Ole. "DEPOSITION OF METHYLCHOLANTHRENE IN SOME ORGANS OF THE RAT.*." Acta Pathologica Microbiologica Scandinavica 20, no. 1 (2009): 79–99. http://dx.doi.org/10.1111/j.1699-0463.1943.tb04787.x.

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23

Ligtenberg, Maarten A., Özcan Çınar, Rikard Holmdahl, Dimitrios Mougiakakos, and Rolf Kiessling. "Methylcholanthrene-Induced Sarcomas Develop Independently from NOX2-Derived ROS." PLOS ONE 10, no. 6 (2015): e0129786. http://dx.doi.org/10.1371/journal.pone.0129786.

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24

Gigliotti, Dulceaydee, Mats Ferm, Hans Wigzell, and Mona Hansson. "A Monoclonal IgM Antibody to a Methylcholanthrene-Induced Tumor." Tumor Biology 12, no. 4 (1991): 217–24. http://dx.doi.org/10.1159/000217707.

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25

Sadek, IA, M. Ghoneum, and EL Cooper. "Effect of 20-methylcholanthrene on amphibian natural killer cells." Diseases of Aquatic Organisms 3 (1987): 155–58. http://dx.doi.org/10.3354/dao003155.

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26

Miao, Wenyu, Zhengwei Fu, and Yuanxiang Jin. "3-Methylcholanthrene alters the hepatic immune response in mice." Acta Biochimica et Biophysica Sinica 52, no. 5 (2020): 570–72. http://dx.doi.org/10.1093/abbs/gmaa020.

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27

Kwon, Yong-Won, Shugo Ueda, Masaya Ueno, Junji Yodoi, and Hiroshi Masutani. "Mechanism of p53-dependent Apoptosis Induced by 3-Methylcholanthrene." Journal of Biological Chemistry 277, no. 3 (2001): 1837–44. http://dx.doi.org/10.1074/jbc.m105033200.

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28

GIGLIOTTI, D., S. TENEBERG, R. ANDFRSSON, et al. "A Monoclonal IgM Antibody to a Methylcholanthrene-Induced Tumour." Scandinavian Journal of Immunology 33, no. 4 (1991): 345–55. http://dx.doi.org/10.1111/j.1365-3083.1991.tb01781.x.

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29

GIMISIS, T., and M. KOREEDA. "ChemInform Abstract: A Highly Efficient Synthesis of 3-Methylcholanthrene." ChemInform 25, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199416134.

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30

Baral, R. N., and P. Maity. "Induction of colorectal cancer in rats by 20-methylcholanthrene." Cancer Letters 61, no. 2 (1992): 177–83. http://dx.doi.org/10.1016/0304-3835(92)90177-w.

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31

Moorthy, Bhagavatula. "3-Methylcholanthrene-inducible hepatic DNA adducts: a mechanistic hypothesis linking sequence-specific DNA adducts to sustained cytochrome P4501A1 induction by 3-methylcholanthrene." Redox Report 7, no. 1 (2002): 9–13. http://dx.doi.org/10.1179/135100002125000127.

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32

Harrington, M. A., F. Gonzales, and P. A. Jones. "Effect of cellular determination on oncogenic transformation by chemicals and oncogenes." Molecular and Cellular Biology 8, no. 10 (1988): 4322–27. http://dx.doi.org/10.1128/mcb.8.10.4322-4327.1988.

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Three developmentally determined myogenic cell lines derived from C3H 10T1/2 C18 (10T1/2) mouse embryo cells treated with 5-azacytidine were compared with the parental 10T1/2 line for their susceptibility to oncogenic transformation by 3-methylcholanthrene or the activated human c-Ha-ras oncogene. Neither the 10T1/2 cells nor the myogenic derivatives grew in soft agar or formed tumors in nude mice. In contrast to 10T1/2 cells, the three myogenic derivatives were not susceptible to transformation by 3-methylcholanthrene, so that cellular determination altered the response of 10T1/2 cells to che

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33

Francovitch, R. J., N. A. Schor, and W. J. George. "Effects of SKF 525A, Phenobarbital, and 3-Methylcholanthrene on Ethylene Dichloride Toxicity Following Inhalation Exposure." Journal of the American College of Toxicology 5, no. 2 (1986): 117–26. http://dx.doi.org/10.3109/10915818609141016.

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The effect of cytochrome P-450-dependent metabolism on ethylene dichloride (EDC) toxicity was investigated in mice. Prior to exposure to EDC, groups of male CD-1 mice were pretreated with phenobarbital or 3-methylcholanthrene to induce metabolism. Other mice were administered SKF 525A before EDC exposure to inhibit cytochrome P-450 metabolism. Following the different pretreatments, mice were exposed to EDC at selected concentrations (1000 ppm, 1250 ppm, or 1500 ppm). Exposure to EDC, without pretreatment, produced a dose-dependent increase in mortality at 24 and 48 hours postexposure. This res

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34

Falany, C. N., M. D. Green, E. Swain та T. R. Tephly. "Substrate specificity and characterization of rat liver p-nitrophenol, 3 α-hydroxysteroid and 17 β-hydroxysteroid UDP-glucuronosyltransferases". Biochemical Journal 238, № 1 (1986): 65–73. http://dx.doi.org/10.1042/bj2380065.

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Purified preparations of rat liver 17-hydroxysteroid, 3-hydroxyandrogen and p-nitrophenol (3-methylcholanthrene-inducible) UDP-glucuronosyltransferases were further characterized as to their substrate specificities, phospholipid-dependency and physical properties. The two steroid UDP-glucuronosyltransferases were shown to exhibit strict stereospecificity with respect to the conjugation of steroids and bile acids. These enzymes have been renamed 17 beta-hydroxysteroid and 3 alpha-hydroxysteroid UDP-glucuronosyltransferase to reflect this specificity for important endogenous substrates. An endog

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35

Harrington, M. A., F. Gonzales, and P. A. Jones. "Effect of cellular determination on oncogenic transformation by chemicals and oncogenes." Molecular and Cellular Biology 8, no. 10 (1988): 4322–27. http://dx.doi.org/10.1128/mcb.8.10.4322.

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Three developmentally determined myogenic cell lines derived from C3H 10T1/2 C18 (10T1/2) mouse embryo cells treated with 5-azacytidine were compared with the parental 10T1/2 line for their susceptibility to oncogenic transformation by 3-methylcholanthrene or the activated human c-Ha-ras oncogene. Neither the 10T1/2 cells nor the myogenic derivatives grew in soft agar or formed tumors in nude mice. In contrast to 10T1/2 cells, the three myogenic derivatives were not susceptible to transformation by 3-methylcholanthrene, so that cellular determination altered the response of 10T1/2 cells to che

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36

Shou, Magang, and Shen K. Yang. "9,10-Dihydroxy-9,10-dihydro-3-methylcholanthrene-2-one: a principal matabolite of the potent carcinogen 3-methylcholanthrene-2-one by rat liver microsomes." Carcinogenesis 11, no. 4 (1990): 689–95. http://dx.doi.org/10.1093/carcin/11.4.689.

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37

Voigt, J. M., F. P. Guengerich, and J. Baron. "Localization and induction of cytochrome P450 1A1 and aryl hydrocarbon hydroxylase activity in rat nasal mucosa." Journal of Histochemistry & Cytochemistry 41, no. 6 (1993): 877–85. http://dx.doi.org/10.1177/41.6.8315279.

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Cytochrome P450 1A1 was localized immunohistochemically and benzo[a]pyrene hydroxylase activity was identified in situ by means of fluorescence histochemistry in the nasal mucosa of untreated, 3-methylcholanthrene-treated or Aroclor 1254-treated rats. Cytochrome P450 1A1 was localized predominantly within Bowman's glands, with considerably less staining occurring in the olfactory epithelium of untreated rats. Similarly, benzo[a]pyrene was hydroxylated to the greatest extent in Bowman's glands and, to a lesser extent, in olfactory epithelial cells. Pre-treatment of tissue sections of nasal muco

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38

Takikawa, O., A. Habara-Ohkubo, and R. Yoshida. "IFN-gamma is the inducer of indoleamine 2,3-dioxygenase in allografted tumor cells undergoing rejection." Journal of Immunology 145, no. 4 (1990): 1246–50. http://dx.doi.org/10.4049/jimmunol.145.4.1246.

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Abstract The depletion of an essential amino acid, tryptophan, caused by induction of indoleamine 2,3-dioxygenase (IDO), has been shown to be a mechanism involving self-defense against inhaled microorganisms and tumor growth. We recently reported that the IDO is dramatically (approximately 50-fold) induced in allografted tumor (3-methylcholanthrene-induced ascites type tumor cells) cells undergoing rejection, and that the enzyme is induced by factor(s) released through the interaction of allografted tumor cells with infiltrating leukocytes. The culture supernatant of infiltrating leukocytes, w

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39

ONO, Yoshiro. "Prophylactic effect of Saiboku-to on methylcholanthrene-induced mouse sarcoma." Okayama Igakkai Zasshi (Journal of Okayama Medical Association) 106, no. 1-2 (1994): 11–21. http://dx.doi.org/10.4044/joma1947.106.1-2_11.

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40

HIGASHIHARA, Tomoko, Toshio TAKESHIMA, Takatoshi KUHARA, Masaru TAJIMA, and Hiroshi TAMURA. "Hematological Changes in the Mice Transplanted with Methylcholanthrene-induced Fibrosarcoma." Experimental Animals 39, no. 3 (1990): 407–11. http://dx.doi.org/10.1538/expanim1978.39.3_407.

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41

Jones, E. J., and D. S. Riddick. "Regulation of constitutive rat hepatic cytochromes P450 by 3-methylcholanthrene." Xenobiotica 26, no. 1 (1996): 995–1012. http://dx.doi.org/10.3109/00498259609062801.

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42

Jones, E. J., and D. S. Riddick. "Regulation of constitutive rat hepatic cytochromes P450 by 3-methylcholanthrene." Xenobiotica 26, no. 10 (1996): 995–1012. http://dx.doi.org/10.3109/00498259609167418.

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43

Haldar, Pallab Kanti, Sanjib Bhattacharya, Asis Bala, Biswakanth Kar, Upal Kanti Mazumder, and Saikat Dewanjee. "Chemopreventive role ofIndigofera aspalathoidesagainst 20-methylcholanthrene-induced carcinogenesis in mouse." Toxicological & Environmental Chemistry 92, no. 9 (2010): 1749–63. http://dx.doi.org/10.1080/02772241003783703.

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44

Moorthy, Bhagavatula, Weiwu Jiang, Lihua Wang, Xanthi Couroucli, and Chu Chun. "Persistent induction of CYP1A1 by 3-methylcholanthrene: Role of CYP1A2." Toxicology Letters 211 (June 2012): S54. http://dx.doi.org/10.1016/j.toxlet.2012.03.214.

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45

Shou, Magang, and Shen K. Yang. "Metabolism of 2S-hydroxy-3-methylcholanthrene by rat liver microsomes." Carcinogenesis 11, no. 11 (1990): 2037–45. http://dx.doi.org/10.1093/carcin/11.11.2037.

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46

Turner, Rhodri T. O., Gareth J. Betts, Awen M. Gallimore, and Claire L. Harris. "The role of complement in 3-methylcholanthrene-induced tumour formation." Molecular Immunology 44, no. 16 (2007): 3950–51. http://dx.doi.org/10.1016/j.molimm.2007.06.099.

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47

Foldes, Robert L., Ronald N. Hines, Kai-Ling Ho, Mei-Ling Shen, Keith B. Nagel, and Edward Bresnick. "3-Methylcholanthrene-induced expression of the cytochrome P-450c gene." Archives of Biochemistry and Biophysics 239, no. 1 (1985): 137–46. http://dx.doi.org/10.1016/0003-9861(85)90820-3.

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48

Noguchi, Y., A. Jungbluth, E. C. Richards, and L. J. Old. "Effect of interleukin 12 on tumor induction by 3-methylcholanthrene." Proceedings of the National Academy of Sciences 93, no. 21 (1996): 11798–801. http://dx.doi.org/10.1073/pnas.93.21.11798.

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49

FORSBERG, JOHN-GUNNAR, and LIV STRAY BREISTEIN. "PROLACTIN AND 3-METHYLCHOLANTHRENE INDUCED CERVICAL CARCINOMA. EFFECT OF BROMOCRIPTINE." Acta Pathologica Microbiologica Scandinavica Section A Pathology 87A, no. 1-6 (2009): 151–56. http://dx.doi.org/10.1111/j.1699-0463.1979.tb00036.x.

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50

Wagman, Lawrence D., and Marianne Z. Metz. "Changes in insulin receptors on methylcholanthrene-induced sarcoma during growth." Journal of Surgical Research 48, no. 5 (1990): 435–39. http://dx.doi.org/10.1016/0022-4804(90)90008-p.

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