The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Heightened uterine mammalian target of rapamycin complex 1 (mTORC1) signaling provokes preterm birth in mice
Open accessAbstract
Although preterm delivery is a major global health issue, its causes and underlying mechanism remain elusive. Using mutant mice, mimicking aspects of human preterm birth, we show here that uterine decidual senescence early in pregnancy via heightened mammalian target of rapamycin complex 1 (mTORC1) signaling is a significant contributor of preterm birth and fetal death, and that these adverse phenotypes are rescued by a low dose of rapamycin, an inhibitor of mTORC1 signaling. This role of mTORC1 signaling in determining the timing of birth in mice may help us better understand the mechanism of the timing of birth in humans and develop new and improved strategies to combat the global problem of preterm birth.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Rapamycin can also prolong the life cycle of many species as diverse as worms and mice, and its signaling system has been implicated as the master regulator of cellular growth and metabolism.”
From Metformin, the Aspirin of the 21st Century: Its Role in Gestational Diabetes Mellitus, Prevention of Preeclampsia and Cancer, and the Promotion of Longevity (2017) · cites this paper as [231]
In the citing paper
“A family of molecules that are the mechanistic target of the rapamycin (mTOR) complex has been attributed a major role in the biology of cell metabolism, growth, longevity, and even preterm birth(230–236).”
From Metformin, the Aspirin of the 21st Century: Its Role in Gestational Diabetes Mellitus, Prevention of Preeclampsia and Cancer, and the Promotion of Longevity (2017) · cites this paper as [231]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Upstream and downstream of mTOR
Hay, N., & Sonenberg, N. (2004) · Genes & Development · doi:10.1101/gad.1212704 · Cited by 4,181
mTOR: from growth signal integration to cancer, diabetes and ageing
Zoncu, R., Efeyan, A., & Sabatini, D. M. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3025 · Cited by 3,941
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766
Toll-like receptors in the induction of the innate immune response
Aderem, A. A., & Ulevitch, R. J. (2000) · Nature · doi:10.1038/35021228 · Cited by 3,082
Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control
Deng, C., Zhang, P., Wade Harper, J., Elledge, S. J., & Leder, P. (1995) · Cell · doi:10.1016/0092-8674(95)90039-x · Cited by 2,113
Franceschi, C., Capri, M., Monti, D., Giunta, S., Olivieri, F., Sevini, F., Panourgia, M. P., Invidia, L., Celani, L., Scurti, M., et al. (2007) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.11.016 · Cited by 2,087
Cellular senescence in cancer and aging.
Collado, M., Blasco, M. A., & Serrano, M. (2007) · Cell · doi:10.1016/j.cell.2007.07.003 · Cited by 1,708
Preterm Birth: Causes, Consequences, and Prevention
Outcomes, A. H., Behrman, R. E., & Butler, A. S. (2007) · Cited by 1,577
Ribosomal Protein S6 Kinase 1 Signaling Regulates Mammalian Life Span
Selman, C., Tullet, J. M. A., Wieser, D., Irvine, E., Lingard, S. J., Choudhury, A. I., Claret, M., Al-Qassab, H., Carmignac, D., Ramadani, F., et al. (2009) · Science · doi:10.1126/science.1177221 · Cited by 1,120 · cited 1×
“There is evidence indicating that increased mTORC1 signaling accelerates the aging process, and that rapamycin (an inhibitor of mTORC1 signaling) or deletion of Rps6k1 (a critical downstream target in mTORC1 signaling) delays this process, thereby extending the life span in various species, including mice (6, 9).”
BackgroundGavazzi, G., & Krause, K.-H. (2002) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(02)00437-1 · Cited by 990
Kwiatkowski, D. J. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.5.525 · Cited by 674
Genetic analysis of ageing: role of oxidative damage and environmental stresses
Martin, G. M., Austad, S. N., & Johnson, T. E. (1996) · Nature Genetics · doi:10.1038/ng0596-25 · Cited by 646
mTORC1 controls fasting-induced ketogenesis and its modulation by ageing
Sengupta, S., Peterson, T. R., Laplante, M., Oh, S., & Sabatini, D. M. (2010) · Nature · doi:10.1038/nature09584 · Cited by 646
Preterm Birth: Causes, Consequences and Prevention
Boardman, J. P. (2008) · Journal of Obstetrics and Gynaecology · doi:10.1080/01443610802243047 · Cited by 552
Beuvink, I., Boulay, A., Fumagalli, S., Zilbermann, F., Ruetz, S., O’Reilly, T., Natt, F., Hall, J., Lane, H. A., & Thomas, G. (2005) · Cell · doi:10.1016/j.cell.2004.12.040 · Cited by 484
Delayed ageing through damage protection by the Arf/p53 pathway
Matheu, A., Maraver, A., Klatt, P., Flores, I., Garcia-Cao, I., Borras, C., Flores, J. M., Viña, J., Blasco, M. A., & Serrano, M. (2007) · Nature · doi:10.1038/nature05949 · Cited by 466
Delayed childbearing and risk of adverse perinatal outcome. A population-based study
Cnattingius, S. (1992) · JAMA · doi:10.1001/jama.268.7.886 · Cited by 347
Early School-Age Outcomes of Late Preterm Infants
Morse, S. B., Zheng, H., Tang, Y., & Roth, J. (2009) · PEDIATRICS · doi:10.1542/peds.2008-1405 · Cited by 330
Nelson, S. M., & Lawlor, D. A. (2011) · PLoS Medicine · doi:10.1371/journal.pmed.1000386 · Cited by 308
Animal models of preterm birth
Elovitz, M. A., & Mrinalini, C. (2004) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2004.10.009 · Cited by 288
Renthal, N. E., Chen, C.-C., Williams, K., Gerard, R. D., Prange‐Kiel, J., & Mendelson, C. R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008301107 · Cited by 288
Marin, T. M., Keith, K., Davies, B., Conner, D. A., Guha, P., Kalaitzidis, D., Wu, X., Lauriol, J., Wang, B., Bauer, M., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44972 · Cited by 285
Paradoxical suppression of cellular senescence by p53
Demidenko, Z. N., Korotchkina, L. G., Gudkov, A. V., & Blagosklonny, M. V. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002298107 · Cited by 273
Feng, Z., Hu, W., Teresky, A. K., Hernando, E., Cordon-Cardo, C., & Levine, A. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708043104 · Cited by 264
Hirota, Y., Daikoku, T., Tranguch, S. L., Xie, H., Bradshaw, H. B., & Dey, S. K. (2010) · Journal of Clinical Investigation · doi:10.1172/jci40051 · Cited by 238
Self-citationLi, F., Igarashi, M., Leung, J., Sugrue, M. M., Lee, S. W., & Aaronson, S. A. (1999) · Oncogene · doi:10.1038/sj.onc.1202615 · Cited by 207
Lorne, E., Zhao, X., Zmijewski, J. W., Liu, G., Park, Y.-J., Tsuruta, Y., & Abraham, E. H. (2009) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0290oc · Cited by 118
Krieg, S. A., Henne, M. B., & Westphal, L. M. (2007) · Fertility and Sterility · doi:10.1016/j.fertnstert.2007.06.014 · Cited by 117
The Graying of the Obstetric Population: Implications for the Older Mother
Carolan, M. C. (2003) · Journal of Obstetric, Gynecologic & Neonatal Nursing · doi:10.1177/0884217502239797 · Cited by 97
Granulated metrial gland cells: A natural killer cell subset of the pregnant murine uterus
Croy, B. A., & Kiso, Y. (1993) · Microscopy Research and Technique · doi:10.1002/jemt.1070250302 · Cited by 92
Normal or stress-induced fibroblast senescence involves COX-2 activity
Zdanov, S., Bernard, D., Debacq‐Chainiaux, F., Martien, S., Gosselin, K., Vercamer, C., Chelli, F., Toussaint, O., & Abbadie, C. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.04.033 · Cited by 68
Jaffer, S., Shynlova, O. P., & Lye, S. J. (2009) · Endocrinology · doi:10.1210/en.2009-0419 · Cited by 54
江島, 邦., Koji, T., Tsuruta, D., Nanri, H., Kashimura, M., & Ikeda, M. (2000) · Biology of Reproduction · doi:10.1095/biolreprod62.1.178 · Cited by 50
Roizen, J. D., Asada, M., Tong, M., Tai, H., & Muglia, L. J. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0178 · Cited by 48
Delayed childbearing — are there any risks?
Roberts, C. L., MARCH, L. M., & Algert, C. S. (1994) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.1994.tb138342.x · Cited by 42
Ikeda, H., Shiojima, I., Oka, T., Yoshida, M., Maemura, K., Walsh, K., Igarashi, T., & Komuro, I. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00732-10 · Cited by 30
Research works printed but not linked: 1
- 10.1001/jama.1992.03490070068044 · DOI
Cited by
Sorted by citations
Programmed cell senescence during mammalian embryonic development
Muñoz-Espín, D., Cañamero, M., Maraver, A., Gómez-López, G., Contreras, J., Murillo-Cuesta, S., Rodríguez-Baeza, A., Varela-Nieto, I., Ruberte, J., Collado, M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.019 · Cited by 1,428
Mechanisms of implantation: strategies for successful pregnancy
Cha, J., Sun, X., & Dey, S. K. (2012) · Nature Medicine · doi:10.1038/nm.3012 · Cited by 1,391
Self-citationEndometrial Decidualization: The Primary Driver of Pregnancy Health
Ng, S., Norwitz, G. A., Pavličev, M., Tilburgs, T., Simón, C., & Norwitz, E. R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114092 · Cited by 358
Romero, R., Erez, O., Hüttemann, M., Maymon, E., Panaitescu, B., Conde-Agudelo, A., Pacora, P., Yoon, B. H., & Grossman, L. I. (2017) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2017.06.003 · Cited by 253
Pathogenesis of preterm birth: bidirectional inflammation in mother and fetus
Green, E. S., & Arck, P. (2020) · Seminars in Immunopathology · doi:10.1007/s00281-020-00807-y · Cited by 228
Metadata
- Authors
- Hirota, Y., Cha, J., Yoshie, M., Daikoku, T., & Dey, S. K.
- Affiliations
- Cincinnati Children's Hospital Medical Center (US)
- Corresponding author
- Dey, Sudhansu K.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2011-10-24
- Volume
- 108
- Issue
- 44
- Pages
- 18073-18078
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3207648
- OpenAlex
- W2107663200
- Cited by
- 125
- References
- 36
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 6 · 2023: 11 · 2022: 6 · 2021: 8 · 2020: 7 · 2019: 8 · 2018: 7 · 2017: 16 · 2016: 9 · 2015: 6 · 2014: 12 · 2013: 10 · 2012: 6
- FWCI
- 6.72
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Bill and Melinda Gates Foundation
- Harvard University
- Takeda Science Foundation
- Uehara Memorial Foundation
- National Institutes of Health (HD12304, DA06668)
- University of Illinois at Urbana-Champaign
- Japan Society for the Promotion of Science (23890045)
- National Institute on Aging (F30AG040858)
- National Institute on Drug Abuse (DA06668, R01DA006668, R37DA006668)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32-HD-07463, R37HD012304, T32HD007463, HD-12304)
- Precursory Research for Embryonic Science and Technology
- Topics
- Health Sciences › Medicine › Obstetrics and Gynecology › Preterm Birth and Chorioamnionitis
- Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- preterm birth, mTORC1 signaling, rapamycin, fetal death, birth timing, decidual cells, mouse model
- MeSH terms
- Mechanistic Target of Rapamycin Complex 1, Animals, Female, Fetal Death, Immunohistochemistry, Proteins, Uterus, Blotting, Western, Signal Transduction, Tumor Suppressor Protein p53, Multiprotein Complexes, Premature Birth, Cyclin-Dependent Kinase Inhibitor p21, Mice, TOR Serine-Threonine Kinases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review