TY - JOUR
T1 - Levamisole potentiation of fluorouracil antiproliferative activity mimicked by orthovanadate, an inhibitor of tyrosine phosphatase
AU - Kovach, John S.
AU - Svingen, Phyllis A.
AU - Schaid, Danial J.
N1 - Funding Information:
Received April 3, 1991; revised December 11, 1991; accepted December 26, 1991. Supported in part by Public Health Service grant CA-31224 and National Cancer Institute-Designated Mayo Comprehensive Cancer Center Core Grant (Pharmacology Core) 15083D3 from the National Cancer Institute, National Institutes of Health, Department of Health and Human Services. J. S. Kovach, P. A. Svingen (Department of Oncology), D. J. Schaid (Health Sciences Research and Cancer Center Statistics), Mayo Foundation, Rochester, Minn. We thank Drs. M. M. Ames, N. Maihle, M. J. O'Connell, and S. Vuk-Pavlovic for review of the manuscript. Correspondence to: John S. Kovach, M.D., Department of Oncology, Mayo Clinic, 200 First St., S.W., Rochester, MN 55905.
PY - 1992/4
Y1 - 1992/4
N2 - Background: Levamisole is an effective antihelminthic drug with immunomodulatory and anticancer activities in model systems. Combined with fluorouracil (5-FU) as adjuvant treatment following resection of Dukes' stage C colon carcinomas, levamisole significantly reduces mortality. However, neither 5-FU nor levamisole alone has a significant effect on survival in this patient group. Previously, we noted that in vitro levamisole potentiated the antiproliferative activity of 5-FU. Purpose: Because levamisole is known to inhibit alkaline phosphatases and has been reported to inhibit dephosphorylation of some membrane phosphoproteins, we studied the effects of levamisole analogues and of chemically unrelated inhibitors of phosphatases for their ability to potentiate 5-FU inhibition of tumor cell line proliferation in vitro.Methods: Human cancer cell lines were exposed to drugs alone or in combination with 5-FU. Antiproliferative activity was measured by determining the extent of reduction of colony formation by the cell lines in test plates compared with control plates. Results:We found that potentiation of 5-FU cytotoxicity by levamisole and by phydroxytetramisole, a metabolite of levamisole, is mimicked by orthovanadate, an inhibitor of tyrosine phosphatases, but not by okadaic acid, an inhibitor of serine and threonine phosphatases. Furthermore, l-p-bromotetramisole, a synthetic analogue of levamisole that is 10-fold more potent in inhibition of alkaline phosphatase than levamisole, potentiates the antiproliferative activity of 5-FU to a greater extent than d-p-bromotetramisole, a stereoisomer of l-p-bromotetramisole with little antiphosphatase activity.Conclusion: Inhibition of tyrosine phosphatases may be responsible for the potentiation by levamisole of the inhibitory activity of 5-FU in vitro. Implications: Inhibition of dephosphorylation of regulatory phosphoproteins may be related to the therapeutic efficacy of the combination of levamisole and 5-FU in the adjuvant treatment of colon carcinoma and may underlie at least some of the multiple effects of levamisole on immune parameters. [J Natl Cancer Inst 84: 515-519, 1992]
AB - Background: Levamisole is an effective antihelminthic drug with immunomodulatory and anticancer activities in model systems. Combined with fluorouracil (5-FU) as adjuvant treatment following resection of Dukes' stage C colon carcinomas, levamisole significantly reduces mortality. However, neither 5-FU nor levamisole alone has a significant effect on survival in this patient group. Previously, we noted that in vitro levamisole potentiated the antiproliferative activity of 5-FU. Purpose: Because levamisole is known to inhibit alkaline phosphatases and has been reported to inhibit dephosphorylation of some membrane phosphoproteins, we studied the effects of levamisole analogues and of chemically unrelated inhibitors of phosphatases for their ability to potentiate 5-FU inhibition of tumor cell line proliferation in vitro.Methods: Human cancer cell lines were exposed to drugs alone or in combination with 5-FU. Antiproliferative activity was measured by determining the extent of reduction of colony formation by the cell lines in test plates compared with control plates. Results:We found that potentiation of 5-FU cytotoxicity by levamisole and by phydroxytetramisole, a metabolite of levamisole, is mimicked by orthovanadate, an inhibitor of tyrosine phosphatases, but not by okadaic acid, an inhibitor of serine and threonine phosphatases. Furthermore, l-p-bromotetramisole, a synthetic analogue of levamisole that is 10-fold more potent in inhibition of alkaline phosphatase than levamisole, potentiates the antiproliferative activity of 5-FU to a greater extent than d-p-bromotetramisole, a stereoisomer of l-p-bromotetramisole with little antiphosphatase activity.Conclusion: Inhibition of tyrosine phosphatases may be responsible for the potentiation by levamisole of the inhibitory activity of 5-FU in vitro. Implications: Inhibition of dephosphorylation of regulatory phosphoproteins may be related to the therapeutic efficacy of the combination of levamisole and 5-FU in the adjuvant treatment of colon carcinoma and may underlie at least some of the multiple effects of levamisole on immune parameters. [J Natl Cancer Inst 84: 515-519, 1992]
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U2 - 10.1093/jnci/84.7.515
DO - 10.1093/jnci/84.7.515
M3 - Article
C2 - 1312177
AN - SCOPUS:0026574170
SN - 0027-8874
VL - 84
SP - 515
EP - 519
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 7
ER -