Navigating a plethora of progesterone receptors: Comments on the safety/ risk of progesterone supplementation in women with a history of breast cancer or at high-risk for developing breast cancer

被引:1
作者
Diep, Caroline H. [1 ]
Mauro, Laura J. [1 ,2 ]
Lange, Carol A. [1 ]
机构
[1] Univ Minnesota, Masonic Canc Ctr, Dept Med, Div Hematol Oncol & Transplantat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Anim Sci, St Paul, MN 55108 USA
基金
美国国家卫生研究院;
关键词
Progesterone; Progestin; Progesterone receptor; Breast cancer; Risk factors; MENOPAUSAL HORMONE-THERAPY; TRANSIENT INCREASE; ESTROGEN; ACTIVATION; PLASTICITY; DOMAINS; PATHWAY; SYSTEM;
D O I
10.1016/j.steroids.2023.109329
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Progesterone and progestin agonists are potent steroid hormones. There are at least three major types of progesterone receptor (PR) families that interact with and respond to progesterone or progestin ligands. These receptors include ligand-activated transcription factor isoforms (PR-A and PR-B) encoded by the PGR gene, often termed classical or nuclear progesterone receptor (nPR), membrane-spanning progesterone receptor membrane component proteins known as PGRMC1/2, and a large family of progestin/adipoQ receptors or PAQRs (also called membrane PRs or mPRs). Cross-talk between mPRs and nPRs has also been reported. The complexity of progesterone actions via a plethora of diverse receptors warrants careful consideration of the clinical applications of progesterone, which primarily include birth control formulations in young women and hormone replacement therapy following menopause. Herein, we focus on the benefits and risk of progesterone/progestin supplementation. We conclude that progesterone-only supplementation is considered safe for most reproductive-age women. However, women who currently have ER + breast cancer or have had such cancer in the past should not take sex hormones, including progesterone. Women at high-risk for developing breast or ovarian cancer, either due to their family history or known genetic factors (such as BRCA1/2 mutation) or hormonal conditions, should avoid exogenous sex hormones and proceed with caution when considering using natural hormones to mitigate menopausal symptoms and/or improve quality of life after menopause. These individuals are urged to consult with a qualified OB-GYN physician to thoroughly assess the risks and benefits of sex hormone supplementation. As new insights into the homeostatic roles and specificity of highly integrated rapid signaling and nPR actions are revealed, we are hopeful that the benefits of using progesterone use may be fully realized without an increased risk of women's cancer.
引用
收藏
页数:5
相关论文
共 36 条
  • [1] Does circulating progesterone mediate the associations of single nucleotide polymorphisms in progesterone receptor (PGR)-related genes with mammographic breast density in premenopausal women?
    Akinjiyan, Favour A.
    Han, Yunan
    Luo, Jingqin
    Toriola, Adetunji T.
    [J]. DISCOVER ONCOLOGY, 2021, 12 (01)
  • [2] Biological Mechanisms and Therapeutic Opportunities in Mammographic Density and Breast Cancer Risk
    Archer, Maddison
    Dasari, Pallave
    Evdokiou, Andreas
    Ingman, Wendy V.
    [J]. CANCERS, 2021, 13 (21)
  • [3] Two domains of the progesterone receptor interact with the estrogen receptor and are required for progesterone activation of the c-Src/Erk pathway in mammalian cells
    Ballaré, C
    Uhrig, M
    Bechtold, T
    Sancho, E
    Di Domenico, M
    Migliaccio, A
    Auricchio, F
    Beato, M
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (06) : 1994 - 2008
  • [4] Hormonal risk factors and invasive epithelial ovarian cancer risk by parity
    Bodelon, C.
    Wentzensen, N.
    Schonfeld, S. J.
    Visvanathan, K.
    Hartge, P.
    Park, Y.
    Pfeiffer, R. M.
    [J]. BRITISH JOURNAL OF CANCER, 2013, 109 (03) : 769 - 776
  • [5] The impact of oral contraceptive use on breast cancer risk: State of the art and future perspectives in the era of 4P medicine
    Bonfiglio, R.
    Di Pietro, M. L.
    [J]. SEMINARS IN CANCER BIOLOGY, 2021, 72 : 11 - 18
  • [6] Progesterone receptor contains a proline-rich motif that directly interacts with SH3 domains and activates c-Src family tyrosine kinases
    Boonyaratanakornkit, V
    Scott, MP
    Ribon, V
    Sherman, L
    Anderson, SM
    Maller, JL
    Miller, WT
    Edwards, DP
    [J]. MOLECULAR CELL, 2001, 8 (02) : 269 - 280
  • [7] Oral contraceptive use by formulation and breast cancer risk by subtype in the Nurses' Health Study II: a prospective cohort study
    Burchardt, Norah A.
    Eliassen, A. Heather
    Shafrir, Amy L.
    Rosner, Bernard
    Tamimi, Rulla M.
    Kaaks, Rudolf
    Tworoger, Shelley S.
    Fortner, Renee T.
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2022, 226 (06) : 821.e1 - 821.e26
  • [8] Chie WC, 2000, AM J EPIDEMIOL, V151, P715, DOI 10.1093/oxfordjournals.aje.a010266
  • [9] Association of Menopausal Hormone Therapy With Breast Cancer Incidence and Mortality During Long-term Follow-up of the Women's Health Initiative Randomized Clinical Trials
    Chlebowski, Rowan T.
    Anderson, Garnet L.
    Aragaki, Aaron K.
    Manson, JoAnn E.
    Stefanick, Marcia L.
    Pan, Kathy
    Barrington, Wendy
    Kuller, Lewis H.
    Simon, Michael S.
    Lane, Dorothy
    Johnson, Karen C.
    Rohan, Thomas E.
    Gass, Margery L. S.
    Cauley, Jane A.
    Paskett, Electra D.
    Sattari, Maryam
    Prentice, Ross L.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 324 (04): : 369 - 380
  • [10] Breast Cancer After Use of Estrogen Plus Progestin and Estrogen Alone Analyses of Data From 2 Women's Health Initiative Randomized Clinical Trials
    Chlebowski, Rowan T.
    Rohan, Thomas E.
    Manson, JoAnn E.
    Aragaki, Aaron K.
    Kaunitz, Andrew
    Stefanick, Marcia L.
    Simon, Michael S.
    Johnson, Karen C.
    Wactawski-Wende, Jean
    O'Sullivan, Mary J.
    Adams-Campbell, Lucile L.
    Nassir, Rami
    Lessin, Lawrence S.
    Prentice, Ross L.
    [J]. JAMA ONCOLOGY, 2015, 1 (03) : 296 - 305