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ABSTRACT: Tumor Prevention by 9-Cis-Retinoic Acid in the N-Nitroso-N-Methylurea
Model of Mammary Carcinogenesis is Potentiated by the Pineal
Hormone Melatonin
Our laboratory has demonstrated that treatment of MCF-7 breast
cancer cells with melatonin (Mlt) followed 24 h later with
physiological concentrations of all-trans retinoic acid (atRA)
results in apoptosis.
These studies were extended into trials using
the N-nitroso-N-methylurea (NMU)-induced rat mammary tumor model.
Initial studies conducted by feeding the animals 9-cis-retinoic
acid (9cRA in the chow) and administering melatonin by subcutaneous
injection in the late afternoon demonstrated that the combination
of Mlt and 9cRA was able to significantly prevent tumor development,
and that the combination was more efficacious that either Mlt or
9cRA alone.
In this report, we conducted studies to determine if
lower doses of 9cRA could be used in combination with Mlt while
still maintaining anti-tumor activity and if the route of administration
of 9cRA (bolus (gavage) v.s. chronic (chow) routes) affected its
interaction with Mlt.
The studies presented here demonstrate that
significantly reduced doses of 9cRA can be used in combination with
Mlt while maintaining anti-tumor efficacy.
Furthermore, our studies
demonstrate that 9cRA is equally effective when it is administered
chronically (chow) or as a bolus (gavage).
These data demonstrate
that the combined use of Mlt and 9cRA produces additive or synergistic
effects, which are more efficacious than 9cRA alone.
This combination
of Mlt and 9cRA could be a potentially useful clinical treatment
regimen for breast cancer since it allows the use of lower doses
of retinoic acid, thus, avoiding the toxic side effects associated
with the use of high dose retinoids.
[04/04/2002; Breast Cancer Research and Treatment]
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