Archives of Toxicology 1999-01-01

Immunotoxicity of the anticancer drug CI-994 in rats: effects on lymphoid tissue.

M J Graziano, A J Galati, K M Walsh

Index: Arch. Toxicol. 73(3) , 168-74, (1999)

Full Text: HTML

Abstract

CI-994 (acetyldinaline) is an investigative oral anticancer drug currently in clinical trials. To characterize the effects of CI-994 on lymphoid tissue, male rats were administered single oral doses at 0 (vehicle control), 10, 23, and 45 mg/kg and killed up to 7 days after dosing for evaluation of white blood cell differentials, bone marrow differentials, lymphoid tissue weights, and selected histopathology of lymphoid tissue. Statistically significant dose-related reductions in blood lymphocytes (CD-3+, CD-4+, CD-8+, CD-20+), monocytes, neutrophils, and bone marrow lymphoid cells were observed in all drug-treated groups on days 1 and/or 3. Statistically significant reductions in bone marrow myeloid cells were also observed on days 1 and 3 at 23 and 45 mg/kg. Complete or partial reversal of most parameters was evident on day 7. Spleen and/or thymus weights were significantly decreased in the groups administered 23 and 45 mg/kg on days 1, 3, and/or 7. Minor reductions in lymphoid organ weights were noted at 10 mg/kg. Minimal to moderate lymphoid depletion of the spleen and thymus was noted on day 3 in animals dosed at 23 mg/kg. In vitro, CI-994 inhibited mitogen-stimulated blood lymphocyte proliferation with a 50% inhibitory concentration (IC50) value of 3 microM. The results demonstrate that CI-994 can effect lymphoid tissue in rats within 1 day of a single oral dose, that effects are generally reversible within 7 days, and that inhibition of lymphocyte proliferation is a sensitive indicator of CI-994 immunotoxicity in vitro.


Related Compounds

Related Articles:

Role of a small molecular weight phosphoprotein in the mechanism of action of CI-994 (N-acetyldinaline).

1995-09-04

[Int. J. Cancer 62(5) , 636-42, (1995)]

Phase I study of oral CI-994 in combination with carboplatin and paclitaxel in the treatment of patients with advanced solid tumors.

2004-01-01

[Cancer Invest. 22(6) , 886-96, (2004)]

Cytotoxic chemotherapy regimens that increase dose per cycle (dose intensity) by extending daily dosing from 5 consecutive days to 28 consecutive days and beyond.

2000-06-01

[Clin. Cancer Res. 6(6) , 2474-81, (2000)]

In vivo development of an acetyldinaline resistant subline of the BN rat acute myelocytic leukemia (BNML).

1993-08-01

[Leukemia 7(8) , 1275-80, (1993)]

Latent hematopoietic stem cell toxicity associated with protracted drug administration.

2001-03-01

[Exp. Hematol. 29(3) , 286-94, (2001)]

More Articles...