Skip to main content

Retinoids: New Developments in Their Mechanism of Action as Related to Control of Proliferative Diseases

  • Conference paper
Retinoids

Abstract

Although there has been recent concern that improper use of retinoids can induce a proliferative reaction in various types of cells (10), there can be little doubt that the basic, physiological role of retinoids is to control proliferative activity in the various secretory and ductular epithelial tissues of the body. This has been known since the original classic observations of Wolbach and Howe (15) on the pathogenesis and histogenesis of vitamin A deficiency in the rat, and is nowhere better stated than in their original paper. They noted that “growth activity of (retinoid-deficient) epithelium is not diminished. On the contrary, there is convincing evidence that it is greatly augmented. In (some of the retinoid-deficient) animals, the behavior of the replacing epithelium in respect to numbers of mitotic figures and response on the part of the connective tissue and blood vessels suggests the acquisition of neoplastic properties … It is highly probable that the epithelium of gland ducts, respiratory mucosa, and genitourinary tract have secretory functions, so that we conclude that the [retinoid] deficiency results in loss of specific chemical functions of the epithelia concerned, while the power of growth becomes augmented.”

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Brinckerhoff CE, McMillan RM, Dayer J-M, Harris ED Jr (1980) Inhibition by retinoic acid of collagenase production in rheumatoid synovial cells. N Engl J Med 303: 432–436

    Article  PubMed  CAS  Google Scholar 

  2. Dayer J-M, Russell RG, Krane SM (1977) Collagenase production by rheumatoid synovial cells: stimulation by a human lymphocyte factor. Science 195: 181–183

    Article  PubMed  CAS  Google Scholar 

  3. De Larco JE, Todaro GJ (1978) Growth factors from murine sarcoma virus-transformed cells. Proc Natl Acad Sci USA 75: 4001–4005

    Article  PubMed  Google Scholar 

  4. Harris ED Jr (1976) Recent insights into the pathogenesis of the proliferative lesion in rheumatoid arthritis. Arthritis Rheum 19: 68–72

    Article  PubMed  Google Scholar 

  5. Harris ED Jr (1980) Pathogenesis of rheumatoid arthritis. In: Textbook of rheumatology. Kelley WN, Harris ED Jr, Ruddy S, Sledge CB (eds). Saunders, Philadelphia, pp 896–922

    Google Scholar 

  6. Harrison SD, Hixson EJ, Burdeshaw JA, Denine EP (1977) Effect of aspirin administration on retinoic acid toxicity in mice. Nature 269: 511–512

    Article  PubMed  CAS  Google Scholar 

  7. Hixson EJ, Denine EP (1978) Effect of nonsteroidal anti-inflammatory agents on toxicity of retinoic acid in mice. Toxicol Appl Pharmacol 45: 317

    Google Scholar 

  8. Levine L, Ohuchi K (1978) Retinoids as well as tumor promoters enhance deacylation of cellular lipids and prostaglandin production in MDCK cells. Nature 276: 274–275

    Article  PubMed  CAS  Google Scholar 

  9. Moon RC, Thompson HJ, Becci PI, Grubbs CJ, Gander RI, Newton DL, Smith JM, Phillips SL, Henderson WR, Mullen LT, Brown CC, Sporn MB (1979) N-(4-hydroxyphenyl) retinamide, a new retinoid for prevention of breast cancer in the rat Cancer Res 39: 1339–1346

    CAS  Google Scholar 

  10. Schroder EW, Black PH (1980) Retinoids: tumor preventers or tumor enhancers? J Natl Cancer Inst 65: 671–674

    PubMed  CAS  Google Scholar 

  11. Sporn MB, Todaro GJ (1980) Autocrine secretion and malignant transformation of cells. N Engl J Med 303: 878–880

    Article  PubMed  CAS  Google Scholar 

  12. Todaro GJ, De Larco JE, Sporn MB (1978) Retinoids block phenotypic cell transformation produced by sarcoma growth factor. Nature 276: 272–274

    Article  PubMed  CAS  Google Scholar 

  13. Welsch CW, Brown CK, Goodrich-Smith M, Chiusano J, Moon RC (1980) Synergistic effect of chronic prolactin suppression and retinoid treatment in the prophylaxis of N-methyl-N-nitrosourea-induced mammary tumorigenesis in female Sprague-Dawley rats. Cancer Res 40: 3095–3098

    PubMed  CAS  Google Scholar 

  14. Welsch CW, Nagasawa H (1977) Prolactin and murine mammary tumorigenesis: a review. Cancer Res 37: 951–963

    PubMed  CAS  Google Scholar 

  15. Wolbach SB, Howe PR (1925) Tissue changes following deprivation of fat-soluble A vitamin. J Exp Med 42: 753–777

    Article  PubMed  CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1981 Springer-Verlag

About this paper

Cite this paper

Sporn, M.B. (1981). Retinoids: New Developments in Their Mechanism of Action as Related to Control of Proliferative Diseases. In: Orfanos, C.E., Braun-Falco, O., Farber, E.M., Grupper, C., Polano, M.K., Schuppli, R. (eds) Retinoids. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68023-6_10

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-68023-6_10

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-68025-0

  • Online ISBN: 978-3-642-68023-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics