Increased mouse epidermal ornithine decarboxylase activity by the tumour promoter 12-O-tetradecanoylphorbol 13-acetate involves increased amounts of both enzyme protein and messenger RNA.

نویسندگان

  • A K Verma
  • D Erickson
  • B J Dolnick
چکیده

Evidence was sought that the tumour promoter 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced mouse epidermal ornithine decarboxylase (ODC, EC 4.1.1.17) activity involves both increased ODC mRNA and ODC protein. Application of 10 nmol of TPA to mouse skin led to a dramatic increase in soluble epidermal ODC activity which paralleled an increase in amount of enzymically active ODC protein as determined by gel electrophoresis of immunoprecipitated difluoromethyl[3H]ornithine-bound ODC. Application of TPA to mouse skin also resulted in an increase in ODC mRNA measured by dot-blot analysis using a radiolabelled cDNA probe. ODC mRNA induction preceded the increase in ODC activity by TPA. TPA-increased ODC mRNA displayed a single major band of 2.1 kilobases in size identified by the Northern blotting procedure.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ornithine decarboxylase activity, cell proliferation, and tumor promotion in mouse epidermis in vivo.

The effect of different phorbol esters and of mechanical treatment on the activity of ornithine decarboxylase in mouse epidermis in vivo was investigated. The strong promoter 12-O-tetradecanoylphorbol-13-acetate as well as the weak promoters phorbol dibenzoate and the 12-O-tetradecanoylphorbol-13-acetate analog 12-O-tetradeca-2-cis, 4-trans-6,8-tetraenoylphorobol-13-acetate strongly increased t...

متن کامل

Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced tumor promotion and epidermal ornithine decarboxylase activity in mouse skin by palmitoylcarnitine.

Palmitoylcarnitine, which has been reported to be an inhibitor of calcium-activated, phospholipid-dependent protein kinase (protein kinase C), inhibited 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced epidermal ornithine decarboxylase in mouse skin in a dose-dependent manner. Neither acetylcarnitine nor palmitic acid inhibited TPA-caused ornithine decarboxylase induction. In addition, palmit...

متن کامل

Inhibition of Tumor Promoter 12-0-Tetradecanoylphorbol-13-acetate-induced Synthesis of Epidermal Ornithine Decarboxylase Messenger RNA and Diacylglycerol-promoted Mouse Skin Tumor Formation by Retinoic Acid1

Evidence is presented that inhibition of 12-O-tetradecanoylphorbol13-acetate (TPA)-induced ornithine decarboxylase (OIK ; EC 4.1.1.17) by retinoic acid may involve inhibition of protein kinase C-mediated synthesis of ODO mRINA. A single application of 10 nmol of TPA to intact mouse skin led to an increase in the steady state levels of epidermal ODC iiiHN \; a maximal level of ODC niRNA occurred...

متن کامل

Vitamin A Acid (Retinoic Acid), a Potent Inhibitor of 12-O- Tetradecanoyl-phorbol-13-acetate-induced Ornithine Decarboxylase Activity in Mouse Epidermis1

Topical application of retinole acid to mouse skin led to a dramatic inhibition of phorbol ester (12-O-tetradecanoylphorbol-13-acetate)-induced epidermal ornithine decarboxylase (EC 4.1.1.17) activity, an event proposed to be essen tial for tumor promotion. The degree of inhibition was de pendent on the dose and time of application of retinoic acid. In contrast, treatment with retinoic acid did...

متن کامل

Vitamin A acid (retinoic acid), a potent inhibitor of 12-O-tetradecanoyl-phorbol-13-acetate-induced ornithine decarboxylase activity in mouse epidermis.

Topical application of retinole acid to mouse skin led to a dramatic inhibition of phorbol ester (12-O-tetradecanoylphorbol-13-acetate)-induced epidermal ornithine decarboxylase (EC 4.1.1.17) activity, an event proposed to be essen tial for tumor promotion. The degree of inhibition was de pendent on the dose and time of application of retinoic acid. In contrast, treatment with retinoic acid did...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Biochemical journal

دوره 237 1  شماره 

صفحات  -

تاریخ انتشار 1986