Contact Dr. Lu for information about cancer treatments。聯繫盧博士，獲取有關癌症治療資訊。
Editor’s note: The title can be a bit misleading. Use any contraceptives do not help prevent breast cancer! The study merely indicates that some contraceptives although based on the same hormone progestins may have lower risk of promoting breast cancer compared to other progestin-based contraceptives . Progestin-based contraceptives have been known to increase risk of breast cancer for long.
The message is useful. Those who choose to use contraceptives can choose one that has a minimal side effect, particularly on the risk of breast cancer and other diseases such as cardiovascular diseases.
編者註：標題可能會引起誤解。 使用任何避孕藥具都無助於預防乳腺癌！ 該研究僅表明某些避孕藥儘管基於相同的激素孕激素可能具有較低的罹患乳腺癌的風險，而其他基於孕激素的避孕藥卻可以增加乳腺癌的風險，這已為人們所熟知。
News Release 28-May-2021
An EPFL study into the distinct biological effects of different progestins on the breast shows that contraceptive-related breast cancer can be prevented by more informed choices about the composition of contraceptives.
Ecole Polytechnique Fédérale de Lausanne
Hormonal contraceptives, e.g. the pill, the patch, and the vaginal ring, contain synthetic hormones that prevent pregnancy by either stopping ovulation, changing the cervical mucus to stop sperm from passing through the cervix and finding an egg, or changing the womb’s lining to prevent a fertilized egg from being implanted in it.
Despite their widespread use, hormonal contraceptives are known to increase the risk of breast cancer, which is the most common cause of cancer-related death among women worldwide, and also topped the list of most commonly diagnosed cancers in 2020.
The main component of hormonal contraceptives are progestins, which, mimic the female sex hormone progesterone. Progesterone is involved in a number of biological processes, including the menstrual cycle, pregnancy, and various aspects of fetal development, like brain programming.
Now, a team of scientists led by Professor Cathrin Brisken at EPFL’s School of Life Sciences, have taken a thorough and close look at the different biological effects that different progestins in hormonal contraceptives have on the breast tissue – the mammary epithelium. The work is published in EMBO Molecular Medicine.
“Although we know how different contraceptive formulations affect the cardiovascular system, we know little about their effects on the breast,” says Brisken. “So we developed new approaches to compare the most commonly used progestins in different hormonal contraceptives and were surprised to find that some of them stimulate cell proliferation in the breast – while others do not.”
The researchers tested the effects of prolonged exposure to different progestins on human breast epithelial cells or HBECs, which line the inner layer of the breast. To do this, they developed “humanized” mouse mammary glands by grafting breast epithelial cells from donated human breast tissue from reduction mammoplasty samples into the animals’ milk ducts and monitoring their growth in vivo.
“We found that HBECs engraft and proliferate in mouse milk ducts, maintaining hormone receptor expression and hormone responsiveness, which are crucial factors for establishing a relevant preclinical model and thereby to foster translational research,” says Brisken.
The team realized that what distinguished the stimulatory and the innocuous progestins were their “androgenic properties” – a technical term for substances that trigger the development of male characteristics, such as body hair, muscle mass etc. This isn’t as strange as it sounds: progesterone, mostly known as a female hormone, is used for the production of the famous male hormone testosterone in both women and men.
Some progestins have androgenic properties, acting like testosterone; some actually block them. The key is a protein known as the androgen receptor, which, when activated by an androgenic progestin, travels into the cell’s nucleus where it regulates the expression of certain genes.
Working with the epithelial cells in a mouse model, the researchers found that androgenic progestins act through the androgen receptor to induce the expression of the protein Rankl, which plays an important role in cell proliferation in the mammary epithelium. This effect was not seen with anti-androgenic progestins.
The study showed that androgenic – but not anti-androgenic – progestins promote cell proliferation. “Exposing human breast epithelia to androgenic progestins for prolonged periods of time caused hyperproliferation and changes in the cells that are associated with early, pre-malignant lesions – at least in xenografted human breast epithelia,” says De Martino.
“Hormonal contraception exposes women to different progestins with or without estrogen,” says Brisken. “The androgenic properties of progestins determine their biological activity in the breast epithelium, and reveal an unexpected role for androgen receptor activity in the proliferation of breast epithelial cells.”
The crucial insight of the study is that progestins with anti-androgenic activity may be a safer option with regards to breast cancer risk than testosterone-related compounds, e.g. the widely used contraceptive levonorgestrel (“Plan B”). “It might be possible to prevent breast cancer associated with contraception by making more informed choices taking the molecular composition of a contraceptive into account,” concludes Brisken.
University Hospital of Lausanne (CHUV)
International Cancer Prevention Institute
Swiss National Science Foundation
Swiss Cancer League
Biltema ISREC Foundation Cancera Stiftelsen
Mats Paulssons Stiftelse
Stitelsen Stefan Paulssons Cancerfond
Joint Action and Learning Initiative (JALI)