Promoters in commercial indoor-plant cultivars of the Euphorbiaceae

Environmental Health Perspectives

Volumn 107, Issue 9, 1999, Pages 753-756

  Vogg, Gerd ^a   Mattes, Elke ^a   Polack, Axel ^b   Sandermann Jr , Heinrich ^a  

^a INSTITUTE OF EPIDEMIOLOGY   (Germany)

^b TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

EBV induction; Euphorbiaceae; Indoor planrs; Ingenol derivatives; Phorbol derivatives; Tumor promotion

Indexed keywords

DITERPENE; EARLY ANTIGEN; ESTER; INGENOL; LUCIFERASE; TUMOR PROMOTER; CARCINOGEN;

ARTICLE; CULTIVAR; EPSTEIN BARR VIRUS; EUPHORBIA; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NONHUMAN; PRIORITY JOURNAL; REPORTER GENE; CELL CULTURE; CHEMISTRY; PLANT;

CODIAEUM VARIEGATUM; EUPHORBIA LEUCONEURA; EUPHORBIA MILII; EUPHORBIA PULCHERRIMA; EUPHORBIACEAE; HUMAN HERPESVIRUS 4;

CARCINOGENS; CELLS, CULTURED; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DITERPENES; EUPHORBIACEAE; PLANTS, TOXIC;

EID: 0033194942     PISSN: 00916765     EISSN: None     Source Type: Journal    
DOI: 10.1289/ehp.99107753     Document Type: Article

References (23)

1. Wolverton BC, Johnson A, Bounds K. Interior Landscape Plants for Indoor Air Pollution Abatement Final Report. John C. Stennis Space Canter, MO:National Aeronautics and Space Administration, 1989.
2. Giese M, Bauer-Doranth U, Langebartels C, Sandermann H. Detoxification of formaldehyde by the spider plant (Chlorophytum comosum L.) and by soybean (Glycine max L.) cell suspension cultures. Plant Physiol 104:1301-1309 (1994).
3. Sandermann H, Nasse B, Langebartels C. Luftreinigung durch Zimmerpflanzen. Eine Beurteilung aus wissenschaftlicher Sicht. In: Reinhaltung der Innenraumluft (Hrsg.: FGU Berlin). Seminar Nr. 33. UTECH '97, Berlin, 17 February 1997. Berlin:Fortbildungszentrum Gesundheitsund Umweltschutz Berlin e.V., 1997;77-88.
4. Wippermann U, Fliegmann J, Bauw G, Langebartels C, Maier K, Sandermann H Jr. Maize glutathione-dependent formaldehyde dehydrogenase: protein sequence and catalytic properties. Planta 208:12-18 (1999).
5. Frohne D, Pfänder HJ. Giftpflanzen. 3: Aufl. Stuttgart, Germany:Wissenschaftl. Verlagsges, 1987.
6. Ott A. Haut und Pflanzen. Berlin:Gustav Fischer Verlag, 1990.
7. Lovell CR. Plants and the Skin. Oxford, U.K.:Blackwell Scientific Publications Editorial Offices, 1993.
8. Hecker E. Co-carcinogene oder bedingt krabsauslösende Faktoren. Naturwissenschaften 65:640-648 (1978).
9. Rauh W. Die großartige Welt der Sukkulenten. 2: Aufl. Berlin:Verlag Paul Parey, 1979.
10. Evans FJ, Soper CJ. The tigliane, daphnane and ingenane diterpenes, their chemistry, distribution and biological activities. A review. Lloydia 41:193-233 (1978).
11. Berenblum I. Cocarcinogenesis. Br Med Bull 4:343-345 (1947).
12. Hecker E. Isolation and characterization of the cocarcinogenic principles from cotton oil. In: Methods in Cancer Research, Vol II (Busch M, ed). New York:Academic Press, 1971;439-484.
13. Kloz U, Hergenhahn M, Fellhauer M, Hecker E. Induction of Epstein-Barr virus antigens by tumor promoters of the diterpene ester type in Raji cells and specific (receptor) binding as compared to irritant and promoting activities. J Cancer Fies Clin Oncol 115:148-156 (1989).
14. Polack A, Laux G, Hergenhahn M, Kloz U, Roeser H, Hecker E, Bomkamm GW. Short term assays for detection of conditional cancerogens. I: Construction of DR-Cat Raji cells and some of their characteristics as tester cells, lnt J Cancer 50:611-616 (1992).
15. Evans FJ, Kinghorn AD. New diesters of 12-deoxy-phorbol. Phytochemistry 14:1669-1670 (1975).
16. Girin MA, Paphassarang S, David-Eteve Ch, Chaboud A, Raynaud J. Determination of ingenol in homeopathic mother tinctures of Euphorbia species by high-performance liquid chromatography. J Chromatogr 637:206-208 (1993).
17. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254 (1976).
18. Vogg G, Mattes E, Rothenburger J, Hertkorn N, Achatz S, Sandermann H. Tumor promoting diterpenes from Euphorbia leuconeura L. Phytochemistry 51:289-295 (1999).
19. Vogg G, Achatz S, Kettrup A, Sandermann H. Tumor promoting diterpenes esters: LC-MS/MS as a fast sensitive and selective detection method. J Chromatogr A (in press).
20. Uemura D, Hirata Y. The isolation and structures of two new alkaloids, milliamines A and B obtained from Euphorbia milii. Tetrahedron Lett 3673-3676 (1971).
21. Marston A, Hecker E. Isolation and biological activities of diterpene anthraniloyl and 3-hydroxyanthraniloyl peptide esters from Euphorbia milii. In: Progress in Tryptophan and Serotonin Research (Schlossberger HG, Kochen W, Linzen B, Steinhart H, eds). Berlin:Walter de Gruyter, 1984:789-792.
22. Zani CL, Marston A, Hamburger M, Hostettmann K. Molluscicidal milliamines from Euphorbia milii var. hislopii. Phytochemistry 34:89-95 (1993).
23. Kinghorn AD, Evans FJ. A biological screen of selected species of the genus Euphorbia for skin irritant effects. Planta Med 28:325-335 (1975).