TAS-108

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TAS-108


TAS-108 is a synthetic steroidal antiestrogen that has been investigated for its potential use in the treatment of breast cancer. It is known for its unique mechanism of action and its ability to act as a selective estrogen receptor modulator (SERM).

Mechanism of Action[edit | edit source]

TAS-108 functions by binding to estrogen receptors in the body, particularly estrogen receptor alpha (ERα) and estrogen receptor beta (ERβ). Unlike other antiestrogens, TAS-108 exhibits both agonist and antagonist properties depending on the tissue type. This dual action allows it to inhibit the growth of estrogen receptor-positive breast cancer cells while potentially offering beneficial effects on other tissues such as bone and the cardiovascular system.

Clinical Development[edit | edit source]

TAS-108 has undergone various phases of clinical trials to evaluate its efficacy and safety in the treatment of breast cancer. These trials have explored its use as a monotherapy as well as in combination with other chemotherapeutic agents. The results have shown promise, particularly in patients who have developed resistance to other forms of hormone therapy.

Potential Benefits[edit | edit source]

One of the significant advantages of TAS-108 over traditional antiestrogens like tamoxifen is its reduced risk of causing endometrial cancer. This is due to its selective action on estrogen receptors, which minimizes the stimulation of the endometrium.

Side Effects[edit | edit source]

The side effects of TAS-108 are generally mild and may include hot flashes, nausea, and fatigue. However, as with any medication, the risk of adverse effects must be weighed against the potential benefits.

Conclusion[edit | edit source]

TAS-108 represents a promising advancement in the field of breast cancer treatment, offering a novel approach to hormone therapy with a potentially improved safety profile. Ongoing research and clinical trials will continue to elucidate its role in cancer therapy.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD