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Abstract

The anticancer affects of Tumor Necrosis Factor Alpha and Tamoxifen have been widely recognized. Our preliminary experiments have revealed that HTB-26 breast cancer cells are nonresponsive to Tamoxifen due to low expression of the estrogen receptor. Other studies have shown that the 5 Azacytidine can stimulate the presence of the estrogen receptor. Experiments were carried out in an attempt to re-stimulate the sensitivity of breast cancer cells to Tamoxifen and measure the death-inducing properities of Tumor Necrosis Factor Alpha. Ideal results would include an increased susceptibility of Tamoxifen after a 5- Azacytidine treatment along with an increase in apoptosis, or programmed cell death.

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