Paper Details
- Home
- Paper Details
Tamoxifen and toremifene lower serum cholesterol by inhibition of delta 8-cholesterol conversion to lathosterol in women with breast cancer.
Author: GyllingH, KangasL, MiettinenT A, MäenpääH, MäntyläE, PyrhönenS
Original Abstract of the Article :
PURPOSE: Long-term effects of tamoxifen and toremifene, a new antiestrogen that closely resembles tamoxifen, were investigated on serum lipids and cholesterol metabolism. PATIENTS AND METHODS: The study group consisted of 24 postmenopausal Finnish women with advanced breast cancer from an internati...See full text at original site
Dr.Camel's Paper Summary Blogラクダ博士について
ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
難解な医学論文を、専門知識のない方にも理解しやすいように、噛み砕いて説明することを目指しています。
* ラクダ博士による解説は、あくまで論文の要点をまとめたものであり、原論文の完全な代替となるものではありません。詳細な内容については、必ず原論文をご参照ください。
* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://doi.org/10.1200/JCO.1995.13.12.2900
データ提供:米国国立医学図書館(NLM)
Tamoxifen and Toremifene: A Powerful Duo Against Cholesterol
The realm of breast cancer treatment continues to evolve, and this study delves into the potential of tamoxifen and toremifene, two antiestrogens with remarkable similarities. The researchers conducted a comprehensive investigation into their long-term effects on serum lipids and cholesterol metabolism in postmenopausal women with advanced breast cancer (n=24) from a larger international study (n=415). The results were quite remarkable. After 12 months of treatment, both tamoxifen and toremifene significantly lowered serum low-density lipoprotein (LDL) cholesterol levels by 16% and 15%, respectively, without altering high-density lipoprotein (HDL) cholesterol or serum triglyceride levels. The study also revealed a fascinating mechanism underlying these effects. Both drugs significantly increased serum delta 8-cholestenol levels, a precursor to cholesterol, suggesting that they inhibit the conversion of this precursor into lathosterol, effectively downregulating cholesterol synthesis. This remarkable finding indicates that the inhibition of the delta 8-isomerase enzyme may be the primary mechanism responsible for the hypolipidemic effects of these drugs.
Lowering Cholesterol, Reducing Risk
These findings suggest that tamoxifen and toremifene hold great promise in reducing the risk of coronary artery disease. The ability of these drugs to lower cholesterol levels through the inhibition of cholesterol synthesis represents a significant step forward in cardiovascular health. Furthermore, the absence of negative effects on HDL cholesterol and triglycerides suggests a favorable lipid profile. These results, coupled with their established efficacy in breast cancer treatment, make these drugs valuable assets in managing the health of women with this disease.
Cardiovascular Health: A Journey Through the Desert
This study highlights the critical link between breast cancer treatment and cardiovascular health. Just as a camel navigates the vast desert, it is essential to consider the multifaceted aspects of health, including cardiovascular risk, when treating breast cancer. The findings suggest that tamoxifen and toremifene may offer a dual benefit, combating both breast cancer and cardiovascular disease. This knowledge empowers women to make informed decisions about their healthcare and adopt a holistic approach to their well-being.
Dr.Camel's Conclusion
This research offers valuable insights into the complex interplay of breast cancer treatment and cardiovascular health. Tamoxifen and toremifene emerge as potent agents that lower cholesterol levels, potentially reducing the risk of coronary artery disease. Remember, managing your health is a journey, and it's essential to be aware of the interconnectedness of various health factors. By staying informed and consulting with your healthcare providers, you can navigate the desert of health challenges with greater confidence and achieve optimal well-being.
Date :
- Date Completed 1996-01-19
- Date Revised 2017-02-10
Further Info :
Related Literature
English
This site uses cookies. Visit our privacy policy page or click the link in any footer for more information and to change your preferences.