Academic Journal

Radiotherapy exposure directly damages the uterus and causes pregnancy loss

التفاصيل البيبلوغرافية
العنوان: Radiotherapy exposure directly damages the uterus and causes pregnancy loss
المؤلفون: Griffiths, M.J., Marshall, S.A., Cousins, F.L., Alesi, L.R., Higgins, J., Giridharan, S., Sarma, U.C., Menkhorst, E., Zhou, W., Care, A.S., Donoghue, J.F., Holdsworth-Carson, S.J., Rogers, P.A.W., Dimitriadis, E., Gargett, C.E., Robertson, S.A., Winship, A.L., Hutt, K.J.
المصدر: http://dx.doi.org/10.1172/jci.insight.163704.
بيانات النشر: American Society for Clinical Investigation
سنة النشر: 2023
المجموعة: The University of Adelaide: Digital Library
مصطلحات موضوعية: Uterus, Placenta, Animals, Humans, Mice, Embryo Implantation, Pregnancy, Placentation, Adolescent, Female, Apoptosis Regulatory Proteins
الوصف: Female cancer survivors are significantly more likely to experience infertility than the general population. It is well established that chemotherapy and radiotherapy can damage the ovary and compromise fertility, yet the ability of cancer treatments to induce uterine damage, and the underlying mechanisms, have been understudied. Here, we show that in mice total-body γ-irradiation (TBI) induced extensive DNA damage and apoptosis in uterine cells. We then transferred healthy donor embryos into ovariectomized adolescent female mice that were previously exposed to TBI to study the impacts of radiotherapy on the uterus independent from effects to ovarian endocrine function. Following TBI, embryo attachment and implantation were unaffected, but fetal resorption was evident at midgestation in 100% of dams, suggesting failed placental development. Consistent with this hypothesis, TBI impaired the decidual response in mice and primary human endometrial stromal cells. TBI also caused uterine artery endothelial dysfunction, likely preventing adequate blood vessel remodeling in early pregnancy. Notably, when pro-apoptotic protein Puma-deficient (Puma–/–) mice were exposed to TBI, apoptosis within the uterus was prevented, and decidualization, vascular function, and pregnancy were restored, identifying PUMA-mediated apoptosis as a key mechanism. Collectively, these data show that TBI damages the uterus and compromises pregnancy success, suggesting that optimal fertility preservation during radiotherapy may require protection of both the ovaries and uterus. In this regard, inhibition of PUMA may represent a potential fertility preservation strategy. ; Meaghan J. Griffiths, Sarah A. Marshall, Fiona L. Cousins, Lauren R. Alesi, Jordan Higgins, Saranya Giridharan, Urooza C. Sarma, Ellen Menkhorst, Wei Zhou, Alison S. Care, Jacqueline F. Donoghue, Sarah J. Holdsworth-Carson, Peter A.W. Rogers, Evdokia Dimitriadis, Caroline E. Gargett, Sarah A. Robertson, Amy L. Winship, and Karla J. Hutt
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 2379-3708
Relation: http://purl.org/au-research/grants/arc/FT190100265; http://purl.org/au-research/grants/arc/DE21010037; NHMRC; JCI Insight, 2023; 8(6):1-20; https://hdl.handle.net/2440/138112; Care, A.S. [0000-0002-0943-9453]; Robertson, S.A. [0000-0002-9967-0084]
DOI: 10.1172/jci.insight.163704
الاتاحة: https://hdl.handle.net/2440/138112
https://doi.org/10.1172/jci.insight.163704
Rights: © 2023, Griffiths et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
رقم الانضمام: edsbas.198A7E05
قاعدة البيانات: BASE
الوصف
تدمد:23793708
DOI:10.1172/jci.insight.163704