Skip to main content
Log in

Effect of retinoic acid on the proliferation and tumorigenicity of mouse mastocytoma cells

Effect of retinoic acid on mastocytoma cells

  • Review
  • Published:
Cytotechnology Aims and scope Submit manuscript

Abstract

Retinoic acid (RA) inhibited the in vitro growth of the mouse mast cell tumor line P815 in a dose- and time-dependent manner. The inhibition was accompanied by an increase in the amount of neutral intracellular mucopolysaccharides. Study of cell cycle kinetics showed that exposure to retinoic acid led to a slowing-down of the cell-cycle progression possibly related to a more differentiated cell population disclosed by microscopy with a lower proliferative capacity.

In vivo, delays in both tumor appearance and mouse mortality were observed after injecting RA into mice bearing mastocytomas. These results suggest that RA could be of interest in the treatment of human malignant systemic mastocytosis with proliferation of immature mast cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. BregmanMD, PetersE, SanderD and MeyskensFL (1983) Dexamethazone, prostaglandin A and retinoic acid modulation of murine and human melanoma cells grown in soft agar. J. Natl. Cancer Inst. 71: 927–932.

    Google Scholar 

  2. BreitmanTR, SelonikSE and CollinsSJ (1980) Induction of differentiation of the human promyelocytic leukemia cell line (HL60) by RA. Proc. Natl. Acad. Sci. USA 77: 2936–2940.

    Google Scholar 

  3. BullagW (1972) Prophylaxis of chemically induced benign and malignant epithelial tumors by vitamin A and retinoic acid. Eur. J. Cancer 8: 689–693.

    Google Scholar 

  4. ChuEW and MalmgrenRA (1965) An inhibitory effect of vitamin A on the induction of tumors of forestomach and cervix in the Syrian hamster by carcinogenic polycyclic hydrocarbons. Canc. Res. 25: 2884–2915.

    Google Scholar 

  5. CraigRW, FrankfurtOS, SakagamiH, TakedaK and BlochA (1984) Macromolecular and cell cycle effects of different classes of agents inducing the maturation of human myeloblastic leukemia (ML-1) cells. Canc. Res. 44: 2421–2429.

    Google Scholar 

  6. CrissmanHA and SteinkampJA (1973) Rapid, simultaneous measurement of DNA, protein and cell volume in single cells from large mammalian cell population. J. Cell Biol. 59: 766–771.

    Google Scholar 

  7. DionLD and GiffordGE (1980) Retinoic acid induces a G1 cell cycle block in Hela cells. Proc. Soc. Exp. Biol. Med. 163: 510–514.

    Google Scholar 

  8. DunnTB and PotterM (1957) A transplantable mast-cell neoplasm in the mouse. J. Natl. Cancer. Inst. 18: 587–595.

    Google Scholar 

  9. FelixEL, LoydB and CohenMH (1975) Inhibition of growth and development of a transplantable murine melanoma by vitamin A. Science 189: 886–888.

    Google Scholar 

  10. HeilmanC and SwarmRL (1975) Effects of thirteen-cis vitamin A acid on chondrosarcoma. Fed. Proc. 34: 822–827.

    Google Scholar 

  11. JettenAM and ShirleyJE (1986) Action of retinoic acid on the diacyl glycerol-induced ornithine decarboxylase activity, reduction of EGF binding and protein kinase C activation in rat tracheal epitelial 2C5 cells. Exp. Cell. Res. 166: 519–525.

    Google Scholar 

  12. JillyD and RayKR (1975) Regulation of growth of mouse mastocytoma cells. Cancer Res. 35: 1495–1502.

    Google Scholar 

  13. KawamuraM and KoshiharaY (1983) Prostaglandin D2 strongly inhibits growth on murine mastocytoma cells. Prostaglandins Leukotrienes Med. 12: 85–93.

    Google Scholar 

  14. LacroixA, AndersonGDL and LippmanME (1980) Retinoids and cultured human fibroblasts effects on cell growth and presence of cellular retinoic acid-binding protein. Exp. Cell. Res. 130: 339–344.

    Google Scholar 

  15. LewisCA, PrattRM, PennypackerJP and HassellJR (1978) Inhibition of limb chondrogenesis in vitro by vitamin A: alterations in cell surface characteristics. Dev. Biol. 64: 31–37.

    Google Scholar 

  16. LippmanSM, KesslerJF, MeyskensML (1987) Retinoids as preventive and therapeutic anticancer agents (part I). Cancer (treatment reports) 71: 391–404.

    Google Scholar 

  17. LotanR, GiottaG, NorckE, NicolsonGL (1978) Characterisation of the inhibitory effects of retinoids on the in vitro growth of two malignant murine melanomas. J. Natl. Cancer Inst. 60: 1035–1041.

    Google Scholar 

  18. LotanR (1980) Effects of vitamin A and its analogs (retinoids) on normal and neoplastic cells. Biochim. Biophys. Acta 605: 33–91.

    Google Scholar 

  19. LudwigKW, LoweyB and NilesRM (1980) Retinoic acid increases cyclic AMP-dependent protein kinase activity in murine melanoma cells. J. Biol. Chem. 255: 5999–6002.

    Google Scholar 

  20. LukGD, CivinCI, WeissmanRM and BaylinSB (1982) Ornithine decarboxylase: essential in proliferation but not differentiation of human promyelocytic leukemia cells. Science 216: 75–77.

    Google Scholar 

  21. MoonRC, GrubbsCJ and SpornMB (1976) Inhibition of 7–12 dimethyl benzanthracene-induced mammary carcinogenesis by retinyl acetate. Cancer Res. 36: 2626–2630.

    Google Scholar 

  22. NilesRM, LoweyB and RogeigS (1986) The effect of retinoic acid on protein phosphorylation in mouse melanoma cells. Exp. Cell. Res. 164: 437–448.

    Google Scholar 

  23. NilesRM (1987) Retinoic acid-induced arrest of mouse melanoma cells in G1 without inhibition of protein synthesis. In vitro 23: 803–804.

    Google Scholar 

  24. PetkovichM, BrandNJ, KrustA and ChambonP (1987) A human retinoic acid receptor which belongs to the family of nuclear receptors. Nature 330: 444–450.

    Google Scholar 

  25. PletA, AvainD and AndersonWB (1986) Effect of retinoic acid treatment of F9 embryonal carcinoma cells on the activity and distribution of cyclic AMP dependent protein kinase. Cancer Res. 46: 2468–2473.

    Google Scholar 

  26. RetturaG, SchitterA, HardyM, LevensonSM, DemetriouA and SeifterE (1975) Brief communication: antitumor action of vitamin A in mice inoculated with adenocarcinoma cells. J. Natl. Cancer Inst. 54: 1489–1491.

    Google Scholar 

  27. SaffiotiU, MontesanoR, SellakumarR and BorgSA (1967) Experimental cancer of the lung. Inhibition by vitamin A of the induction of tracheobronchial squamous metaplasia and squamous cell tumors. Cancer 20: 857–864.

    Google Scholar 

  28. ShapiroS (1986) Retinoids and epithelial differentiation. In: ShermanMI (eds) Retinoids and Cell Differentiation, CRC-Press, Boca Raton, Florida, p. 29.

    Google Scholar 

  29. ShermanMI (1986) Cellular retinoid-binding proteins. In ShermanMI (eds) Retinoids and Cell Differentiation, CRC. Press, Inc. Boca Raton, Florida, p. 165.

    Google Scholar 

  30. SpornMB, SquireRA, BrownCC, SmithJM, WenkML and SpringerS (1977) 13-cis retinoic acid inhibition of bladder carcinogenesis in the rat. Science 195: 487–489.

    Google Scholar 

  31. TraganosF, BuetiC, DarzynkiewiczZ and MelamedMR (1984) Effects of retinoic acid versus dimethyl sulfoxide on friend erythroleukemia cell growth. I cell proliferation, RNA content and protein content. J. Natl. Cancer Inst. 73: 193–204.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nafziger, J., Kaicer, E., Ronot, X. et al. Effect of retinoic acid on the proliferation and tumorigenicity of mouse mastocytoma cells. Cytotechnology 2, 111–118 (1989). https://doi.org/10.1007/BF00386143

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00386143

Key words

Navigation