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Is digitalis a therapy for breast carcinoma?
1Institute of Pathology, University of Uppsala, Uppsala, Sweden.
Abstract:
We have previously reported effects on breast carcinoma by digitalis on patients in vivo with significant effects on cytometric features and recurrence rate. Increased attention is now paid to the anti-proliferative and apoptosis inducing effect on cancer cells in vitro by glycosides from foxglove as well as by some other glycosides. The present study is a long-term follow-up (22.3 years) of 175 patients with breast carcinoma, of which 32 were on digitalis treatment, when they acquired their breast carcinoma. There was a lower death rate (6%) from breast carcinoma among the patients on digitalis, when compared with patients not on digitalis (34%). Also proliferation/aneuploidy was less pronounced of the tumors in patients on digitalis. These observations were statistically significant although the statistical analysis was hampered in the life-table analysis by the fact that only 2/32 patients on digitalis died from breast cancer. Serious consideration should be given to the effects of digitalis derivatives on cancer cells in cancer drug design. This field of research is not sufficiently explored and holds promise to contain drugs superior to present-day adjuvant therapy both with respect to effects and side-effects.
Insights
Digitalis treatment in breast carcinoma patients showed a significantly lower death rate and reduced tumor proliferation. These findings suggest digitalis derivatives may offer promising therapeutic potential for cancer drug design.
Area of Science:
- Oncology
- Pharmacology
- Cardiology
Background:
- Previous studies indicated digitalis affects breast carcinoma cytometric features and recurrence.
- Current research focuses on the anti-proliferative and apoptosis-inducing effects of digitalis glycosides on cancer cells.
- Digitalis, a cardiac glycoside, has a long history of medicinal use.
Purpose of the Study:
- To conduct a long-term follow-up study on breast carcinoma patients treated with digitalis.
- To evaluate the impact of digitalis on mortality rates and tumor characteristics in breast cancer patients.
- To explore the potential of digitalis derivatives in cancer drug development.
Main Methods:
- Long-term follow-up (22.3 years) of 175 breast carcinoma patients.
- Comparison of outcomes between 32 patients on digitalis treatment and those not on digitalis.
- Analysis of death rates, tumor proliferation, and aneuploidy.
Main Results:
- A significantly lower death rate from breast carcinoma in patients on digitalis (6%) compared to those not on digitalis (34%).
- Reduced tumor proliferation and aneuploidy observed in patients treated with digitalis.
- Statistical significance was noted, though limited by a low number of deaths in the digitalis group.
Conclusions:
- Digitalis derivatives warrant serious consideration for cancer drug design due to observed effects on cancer cells.
- The potential of digitalis in cancer therapy may surpass current adjuvant treatments in efficacy and side-effect profiles.
- Further research into digitalis's role in oncology is crucial and holds significant promise.
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