Promoting neoplastic transformation of humic acid in mouse epidermal JB6 Cl41 cells

Chemico-Biological Interactions

Volumn 162, Issue 3, 2006, Pages 249-258

  Lu, Fung Jou ^a   Tseng, Tsui Hwa ^a   Lee, Wei Jiunn ^a   Yen, Cheng Chieh ^a   Yin, Yu Fang ^a   Liao, Chin Wei ^a   Liu, Kuan Miao ^a  

^a CHUNG SHAN MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Humic acid; Promotion; Transformation

Indexed keywords

ACETYLCYSTEINE; ANTIOXIDANT; HUMIC ACID; REACTIVE OXYGEN METABOLITE;

ANIMAL CELL; ANIMAL CELL CULTURE; ARTICLE; CELL ASSAY; CELL CLONE; CELL CONTACT; CELL GROWTH; CELL MIGRATION; CELL TRANSFORMATION; CONTROLLED STUDY; DRUG EFFECT; DRUG MECHANISM; EPIDERMIS CELL; FILOPODIUM; IN VITRO STUDY; MALIGNANT TRANSFORMATION; MOUSE; NONHUMAN; SPINDLE CELL; TUMOR PROMOTION; WOUND HEALING;

ANIMALS; CELL DEATH; CELL LINE; CELL MOVEMENT; CELL TRANSFORMATION, NEOPLASTIC; EPIDERMIS; HUMIC SUBSTANCES; MICE; OXIDATION-REDUCTION;

EID: 33748747692     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2006.07.007     Document Type: Article

References (33)

1. Cheng M.L., Ho H.Y., Chiu T.Y., and Lu F.J. Humic acid-mediated oxidative damage to human erythrocytes: a possible mechanism leading to anemia in Blackfoot disease. Free Radic. Biol. Med. 27 (1999) 470-477
2. Liang H.J., Tsai C.L., Chen P.Q., and Lu F.J. Oxidative injury induced by synthetic humic acid polymer and monomer in cultured rabbit articular chondrocytes. Life Sci. 65 (1999) 1163-1173
3. Gau R.J., Yang H.L., Suen J.L., and Lu F.J. Induction of oxidative stress by humic acid through increasing intracellular iron: a possible mechanism leading to atherothrombotic vascular disorder in Blackfoot disease. Biochem. Biophys. Res. Commun. 283 (2001) 743-749
4. Yang M.L., Lee Y., Huang T.S., and Lu F.J. Humic acid extracted from Blackfoot disease-endemic well water induces adipocyte differentiation of C3H10T1/2 fibroblast cells: a possible mechanism leading to atherosclerotic-like plaque in Blackfoot disease. Arch. Toxicol. 76 (2002) 48-54
5. Lu F.J. Fluorescent humic substances and Blackfoot disease in Taiwan. Appl. Organomet. Chem. 4 (1990) 191-195
6. Zhai S.S., Kimbrough R.D., Meng B., Han J.Y., Levoid M., Hou X., and Yin X.N. Kashin-Beck disease: a cross-sectional study in seven villages in the People's Republic of China. J. Toxicol. Environ. Health 30 (1990) 239-259
7. Cookesy R.C., Gaitan E., Lindsay R.J., Hill J.R., and Keely K. Humic substances, a possible source of environmental goitrogens. Org. Geochem. 8 (1985) 77-80
8. Lu F.J., Guo H.R., Chiangs H.S., and Hong C.L. Relationships between the fluorescent intensity of well water and the incidence rate of bladder cancer. J. Chin. Oncol. Soc. 2 (1986) 14-23
9. Cheng M.L., Ho H.Y., Huang Y.W., Lu F.J., and Chiu T.Y. Humic acid induces oxidative DNA damage, growth retardation, and apoptosis in human primary fibroblasts. Exp. Biol. Med. 228 (2003) 413-423
10. Bernacchi F., Ponzanelli I., Minunni M., Falezza A., Loprieno N., and Barale R. In vivo cytogenetic effects of natural humic acid. Mugagenesis 11 (1996) 467-469
11. +-ATPase activity in maize roots. Plant Physiol. 130 (2002) 1951-1957
12. Takahashi K., Heine U.I., Junker J.L., Colburn N.H., and Rice J.M. Role of cytoskeleton changes and expression of the H-ras oncongene during promotion of neoplastic transformation in mouse epidermal JB6 cells. Cancer Res. 46 (1986) 5923-5932
13. Suzukawa K., Weber T.J., and Colburn N.H. AP-1, NFkB, and ERK activation thresholds for promotion of neoplastic transformation in the mouse epidermal JB6 model. Environ. Health Perspect. 110 (2002) 865-870
14. Samuel S., and Bernstein L.R. Adhesion, migration, transcriptional, interferon-inducible, and other signaling molecules newly implicated in cancer susceptibility and resistance of JB6 cells by cDNA microarray analyses. Mol. Carcinogenesis 39 (2004) 34-60
15. Finkel T. Oxidant signals and oxidative stress. Curr. Opin. Cell Biol. 15 (2003) 47-245
16. Schnitzers M.T. Organic matter characterization. In: Page A.L. (Ed). Methods of Soil Analysis. Part 2. Chemical and Microbiological Properties (1982), Academic Press, New York, NY 581-594
17. Frazelle J.H., Abernethy D.J., and Boreiko C.J. Factors influencing the promotion of transformation in chemically-initiated C3H10T1/2C18 mouse embryo fibroblasts. Carcinogenesis 4 (1983) 709-715
18. Bonini M.G., Rota C., Tomasi A., and Mason R.P. The oxidation of 2′,7′-dichlorofluorescin to reactive oxygen species: a self-fulfilling prophesy?. Free Radic. Biol. Med. 40 (2006) 968-975
19. Qian Y., Luo J., and Leonard S.S. Hydrogen peroxide formation and actin filament reorganization by Cdc42 are essential for ethanol-induced in vitro angiogenesis. J. Biol. Chem. 278 (2003) 16189-16197
20. Carter C.A., Doherty M.M., Rusnak D.W., Nettesheim P., and Ferriola P.C. Alterations in the localization of F-actin, fibronectin, and thromospondin occur prior to neoplastic transformation in rat tracheal epithelial cells. Exp. Cell Res. 212 (1994) 141-150
21. Colburn N.H., Former B.F., Nelson K.A., and Yuspa S.H. Tumor promoter induces anchorage independence irreversibly. Nature 281 (1979) 589-591
22. Cheng T.T., and Heidelberger C. In vitro malignant transformation of cells derived from mouse prostate in the presence of 3-methylcholanthrene. J. Natl. Cancer Inst. 42 (1969) 915-925
23. Namba M., Masuji H., and Sato J. Carcinogenesis in tissue culture IX Malignant transformation in cultured rat cells treated with 4-nitroquinoline-N-oxide. Jpn. J. Exp. Med. 39 (1969) 1770-1772
24. Chen C.C., Tseng T.H., Hsu J.D., and Wang C.J. Tumor promoting effect of GGN-MRP extract from the maillard reaction products of glucose and glycine in the presence of sodium nitrite in C3H10T1/2 cells. J. Agric. Food Chem. 49 (2001) 6063-6067
25. Marks F., and Furstenberger G. The conversion stage of skin carcinogenesis. Carcinogenesis 11 (1990) 2085-2092
26. Monteiro H.P., and Stern A. Redox modulatin of tyrosine phosphorylation-dependent signal transduction pathways. Free Radic. Biol. Med. 21 (1996) 323-333
27. Szatrowski T.P., and Nathan C.F. Production of large amounts of hydrogen peroxide by human tumor cells. Cancer Res. 51 (1991) 794-798
28. Kuo H.C., Kuo W.H., Lee Y.J., Lin W.L., Chou F.P., and Tseng T.H. Inhibitory effect of caffeic acid phenethyl ester on the growth of C6 glioma cells in vitro and in vivo. Cancer Lett. 234 (2006) 199-208
29. Owuor E.D., and Kong A.N. Antioxidants and oxidants regulated signal transduction pathways. Biochem. Pharmacol. 64 (2002) 765-770
30. Hsu T.C., Young M.R., Cmarik J., and Colburn N.H. Activator protein (AP-1)- and nuclear factor kB (NF-KB)-dependent transcriptional events in carcinogenesis. Free Radic. Biol. Med. 28 (2000) 338-1384
31. Yang M.L., Hunag T.S., Lee Y., Chen T.H., Chen S.Y., and Lu F.J. Inhibition of endogenous thyroid hormone receptor-β and peroxisome proliferator-activated receptor-α activities by humic acid in a human-derived liver cell line. Thyroid 12 (2002) 361-371
32. Perchellet J.P., Perchellet E.M., Gali H.U., and Gao X.M. Oxidative stress and multistage skin carcinogenesis. In: Mukhtar H. (Ed). Skin Cancer: Mechanisms and Human Relevance (1995), CRC press, Boca Raton, FL 145
33. Castro G.D., de Castro C.R., Maciel M.E., Fanelli S.L., de Ferreyra E.C., Gomez M.I., and Castro J.A. Ethanol-induced oxidative stress and acetaldehyde formation in rat mammary tissue: potential factors involved in alcohol drinking promotion of breast cancer. Toxicology 219 (2006) 208-219