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The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1982 Feb;69(2):277–283. doi: 10.1172/JCI110450

Retinoic acid. Inhibition of the clonal growth of human myeloid leukemia cells.

D Douer, H P Koeffler
PMCID: PMC370976  PMID: 6276439

Abstract

Vitamin A and its analogues (retinoids) affect normal and malignant hematopoietic cells. We examined the effect of retinoids on the clonal growth in vitro of myeloid leukemia cells. Retinoic acid inhibited the clonal growth of the KG-1, acute myeloblastic leukemia, and the HL-60, acute promyelocytic leukemia, human cell lines. The KG-1 cells were extremely sensitive to retinoic acid, with 50% of the colonies inhibited by 2.4-nM concentrations of the drug. A 50% growth inhibition of HL-60 was achieved by 25 nM retinoic acid. Complete inhibition of growth of both leukemia cell lines was seen with 1 microM retinoic acid. Exposure of KG-1 cells to retinoic acid for only 3-5 d was sufficient to inhibit all clonal growth. The all-trans and 13-cis forms of retinoic acid were equally effective in inhibiting proliferation. Retinal, retinyl acetate, and retinol (vitamin A) were less potent inhibitors. Clonal growth of the human K562 and mouse M-1 myeloid leukemic cell lines was not affected by 10 microM retinoic acid. Retinoic acid also inhibited the clonal growth of leukemia cells from five of seven patients with acute myeloid leukemia. Retinoic acid at concentrations of 5 nM to 0.3 microM inhibited 50% clonal growth, and 1 microM retinoic acid inhibited 64-98% of the leukemic colonies. The inhibition of clonal growth of KG-1 and HL-60 cell lines and of leukemic cells from two patients was not associated with the presence of a specific cytoplasmic retinoic acid-binding protein. Our study suggests that retinoic acid may prove to be effective in the treatment of human myeloid leukemia.

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Selected References

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  1. Breitman T. R., Collins S. J., Keene B. R. Terminal differentiation of human promyelocytic leukemic cells in primary culture in response to retinoic acid. Blood. 1981 Jun;57(6):1000–1004. [PubMed] [Google Scholar]
  2. Breitman T. R., Selonick S. E., Collins S. J. Induction of differentiation of the human promyelocytic leukemia cell line (HL-60) by retinoic acid. Proc Natl Acad Sci U S A. 1980 May;77(5):2936–2940. doi: 10.1073/pnas.77.5.2936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Classification of acute leukemia. Ann Intern Med. 1977 Dec;87(6):740–753. doi: 10.7326/0003-4819-87-6-740. [DOI] [PubMed] [Google Scholar]
  4. Collins S. J., Gallo R. C., Gallagher R. E. Continuous growth and differentiation of human myeloid leukaemic cells in suspension culture. Nature. 1977 Nov 24;270(5635):347–349. doi: 10.1038/270347a0. [DOI] [PubMed] [Google Scholar]
  5. De Luca L. M., Frot-Coutaz J. P., Silverman-Jones C. S., Roller P. R. Chemical synthesis of phosphorylated retinoids. Their mannosyl acceptor activity in rat liver membranes. J Biol Chem. 1977 Apr 25;252(8):2575–2579. [PubMed] [Google Scholar]
  6. Duttera M. J., Whang-Peng J., Bull J. M., Carbone P. P. Cytogenetically abnormal cells in vitro in acute leukaemia. Lancet. 1972 Apr 1;1(7753):715–718. doi: 10.1016/s0140-6736(72)90231-0. [DOI] [PubMed] [Google Scholar]
  7. Frolik C. A., Tavela T. E., Peck G. L., Sporn M. B. High-pressure liquid chromatographic determination of 13-cis-retinoic acid and all-trans-retinoic acid in human plasma. Anal Biochem. 1978 Jun 1;86(2):743–750. doi: 10.1016/0003-2697(78)90802-3. [DOI] [PubMed] [Google Scholar]
  8. Golde D. W., Quan S. G., Cline M. J. Human T lymphocyte cell line producing colony-stimulating activity. Blood. 1978 Nov;52(5):1068–1072. [PubMed] [Google Scholar]
  9. Harisiadis L., Miller R. C., Hall E. J., Borek C. A vitamin A analogue inhibits radiation-induced oncogenic transformation. Nature. 1978 Aug 3;274(5670):486–487. doi: 10.1038/274486a0. [DOI] [PubMed] [Google Scholar]
  10. Ichikawa Y. Differentiation of a cell line of myeloid leukemia. J Cell Physiol. 1969 Dec;74(3):223–234. doi: 10.1002/jcp.1040740303. [DOI] [PubMed] [Google Scholar]
  11. Jetten A. M., Jetten M. E. Possible role of retinoic acid binding protein in retinoid stimulation of embryonal carcinoma cell differentiation. Nature. 1979 Mar 8;278(5700):180–182. doi: 10.1038/278180a0. [DOI] [PubMed] [Google Scholar]
  12. Jetten A. M., Jetten M. E., Shapiro S. S., Poon J. P. Characterization of the action of retinoids on mouse fibroblast cell lines. Exp Cell Res. 1979 Mar 15;119(2):289–299. doi: 10.1016/0014-4827(79)90356-2. [DOI] [PubMed] [Google Scholar]
  13. Jones H., Blanc D., Cunliffe W. J. 13-cis retinoic acid and acne. Lancet. 1980 Nov 15;2(8203):1048–1049. doi: 10.1016/s0140-6736(80)92273-4. [DOI] [PubMed] [Google Scholar]
  14. Koeffler H. P., Golde D. W. Acute myelogenous leukemia: a human cell line responsive to colony-stimulating activity. Science. 1978 Jun 9;200(4346):1153–1154. doi: 10.1126/science.306682. [DOI] [PubMed] [Google Scholar]
  15. Koeffler H. P., Golde D. W. Human myeloid leukemia cell lines: a review. Blood. 1980 Sep;56(3):344–350. [PubMed] [Google Scholar]
  16. Lacroix A., Lippman M. E. Binding of retinoids to human breast cancer cell lines and their effects on cell growth. J Clin Invest. 1980 Mar;65(3):586–591. doi: 10.1172/JCI109703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lotan R. Effects of vitamin A and its analogs (retinoids) on normal and neoplastic cells. Biochim Biophys Acta. 1980 Mar 12;605(1):33–91. doi: 10.1016/0304-419x(80)90021-9. [DOI] [PubMed] [Google Scholar]
  18. Lotan R., Neumann G., Lotan D. Relationships among retinoid structure, inhibition of growth, and cellular retinoic acid-binding protein in cultured S91 melanoma cells. Cancer Res. 1980 Apr;40(4):1097–1102. [PubMed] [Google Scholar]
  19. Lotan R., Nicolson G. L. Inhibitory effects of retinoic acid or retinyl acetate on the growth of untransformed, transformed, and tumor cells in vitro. J Natl Cancer Inst. 1977 Dec;59(6):1717–1722. doi: 10.1093/jnci/59.6.1717. [DOI] [PubMed] [Google Scholar]
  20. Lotan R., Ong D. E., Chytil F. Comparison of the level of cellular retinoid-binding proteins and susceptibility to retinoid-induced growth inhibition of various neoplastic cell lines. J Natl Cancer Inst. 1980 May;64(5):1259–1262. [PubMed] [Google Scholar]
  21. Lozzio C. B., Lozzio B. B. Human chronic myelogenous leukemia cell-line with positive Philadelphia chromosome. Blood. 1975 Mar;45(3):321–334. [PubMed] [Google Scholar]
  22. Merriman R. L., Bertram J. S. Reversible inhibition by retinoids of 3-methylcholanthrene-induced neoplastic transformation in C3H/10T1/2 clone 8 cells. Cancer Res. 1979 May;39(5):1661–1666. [PubMed] [Google Scholar]
  23. Moon R. C., Grubbs C. J., Sporn M. B., Goodman D. G. Retinyl acetate inhibits mammary carcinogenesis induced by N-methyl-N-nitrosourea. Nature. 1977 Jun 16;267(5612):620–621. doi: 10.1038/267620a0. [DOI] [PubMed] [Google Scholar]
  24. Ong D. E., Chytil F. Retinoic acid-binding protein in rat tissue. Partial purification and comparison to rat tissue retinol-binding protein. J Biol Chem. 1975 Aug 10;250(15):6113–6117. [PubMed] [Google Scholar]
  25. Ong D. E., Page D. L., Chytil F. Retinoic acid binding protein: occurrence in human tumors. Science. 1975 Oct 3;190(4209):60–61. doi: 10.1126/science.1166300. [DOI] [PubMed] [Google Scholar]
  26. Peck G. L., Olsen T. G., Yoder F. W., Strauss J. S., Downing D. T., Pandya M., Butkus D., Arnaud-Battandier J. Prolonged remissions of cystic and conglobate acne with 13-cis-retinoic acid. N Engl J Med. 1979 Feb 15;300(7):329–333. doi: 10.1056/NEJM197902153000701. [DOI] [PubMed] [Google Scholar]
  27. Sachs L. Control of normal cell differentiation and the phenotypic reversion of malignancy in myeloid leukaemia. Nature. 1978 Aug 10;274(5671):535–539. doi: 10.1038/274535a0. [DOI] [PubMed] [Google Scholar]
  28. Schindler J., Matthaei K. I., Sherman M. I. Isolation and characterization of mouse mutant embryonal carcinoma cells which fail to differentiate in response to retinoic acid. Proc Natl Acad Sci U S A. 1981 Feb;78(2):1077–1080. doi: 10.1073/pnas.78.2.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Sporn M. B., Dunlop N. M., Newton D. L., Smith J. M. Prevention of chemical carcinogenesis by vitamin A and its synthetic analogs (retinoids). Fed Proc. 1976 May 1;35(6):1332–1338. [PubMed] [Google Scholar]
  30. Strickland S., Mahdavi V. The induction of differentiation in teratocarcinoma stem cells by retinoic acid. Cell. 1978 Oct;15(2):393–403. doi: 10.1016/0092-8674(78)90008-9. [DOI] [PubMed] [Google Scholar]

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