Plasma cell-free DNA concentration increases during luteolysis in beef cows.
cfDNA
corpus luteum
Journal
Reproduction in domestic animals = Zuchthygiene
ISSN: 1439-0531
Titre abrégé: Reprod Domest Anim
Pays: Germany
ID NLM: 9015668
Informations de publication
Date de publication:
Sep 2023
Sep 2023
Historique:
revised:
16
05
2023
received:
12
04
2023
accepted:
29
06
2023
medline:
8
9
2023
pubmed:
4
7
2023
entrez:
4
7
2023
Statut:
ppublish
Résumé
During cell death, DNA is fragmented and reaches the bloodstream in the form of cell-free DNA (cfDNA). Luteal cells must undergo an apoptotic process during structural luteolysis to begin a new oestrous cycle. We hypothesized that cfDNA concentrations would increase when inducing luteolysis by applying prostaglandin F
Substances chimiques
Dinoprost
B7IN85G1HY
Progesterone
4G7DS2Q64Y
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1334-1337Subventions
Organisme : Departamento Administrativo de Ciencia, Tecnología e Innovación (COLCIENCIAS)
Organisme : Institute of Food and Agricultural Sciences, University of Florida
Informations de copyright
© 2023 Wiley-VCH GmbH. Published by John Wiley & Sons Ltd.
Références
Choudhary, E., Sen, A., Inskeep, E. K., & Flores, J. A. (2005). Developmental sensitivity of the bovine corpus luteum to prostaglandin F2α (PGF2α) and Endothelin-1 (ET-1): Is ET-1 a mediator of the luteolytic actions of 2α or a tonic inhibitor of progesterone secretion? Biology of Reproduction, 72(3), 633-642. https://doi.org/10.1095/biolreprod.104.034736
Cicchillitti, L., Corrado, G., de Angeli, M., Mancini, E., Baiocco, E., Patrizi, L., Zampa, A., Merola, R., Martayan, A., Conti, L., Piaggio, G., & Vizza, E. (2017). Circulating cell-free DNA content as blood based biomarker in endometrial cancer. Oncotarget, 8(70), 115230-115243. https://doi.org/10.18632/ONCOTARGET.23247
Fleischhacker, M., & Schmidt, B. (2007). Circulating nucleic acids (CNAs) and cancer-a survey. Biochimica et Biophysica Acta-Reviews on Cancer, 1775(1), 181-232. https://doi.org/10.1016/J.BBCAN.2006.10.001
Herzog, K., Brockhan-Lüdemann, M., Kaske, M., Beindorff, N., Paul, V., Niemann, H., & Bollwein, H. (2010). Luteal blood flow is a more appropriate indicator for luteal function during the bovine estrous cycle than luteal size. Theriogenology, 73(5), 691-697. https://doi.org/10.1016/j.theriogenology.2009.11.016
Kliem, H., Berisha, B., Meyer, H. H. D., & Schams, D. (2009). Regulatory changes of apoptotic factors in the bovine corpus luteum after induced luteolysis. Molecular Reproduction and Development, 76(3), 220-230. https://doi.org/10.1002/mrd.20946
Miyamoto, A., Shirasuna, K., Wijayagunawardane, M. P. B., Watanabe, S., Hayashi, M., Yamamoto, D., Matsui, M., & Acosta, T. J. (2005). Blood flow: A key regulatory component of corpus luteum function in the cow. Domestic Animal Endocrinology, 29(2), 329-339. https://doi.org/10.1016/j.domaniend.2005.03.011
Neuvians, T. P., Schams, D., Berisha, B., & Pfaffl, M. W. (2004). Involvement of pro-inflammatory cytokines, mediators of inflammation, and basic fibroblast growth factor in prostaglandin F2α-induced luteolysis in bovine corpus luteum1. Biology of Reproduction, 70(2), 473-480. https://doi.org/10.1095/biolreprod.103.016154
Pohler, K. G., Pereira, M. H. C., Lopes, F. R., Lawrence, J. C., Keisler, D. H., Smith, M. F., Vasconcelos, J. L. M., & Green, J. A. (2016). Circulating concentrations of bovine pregnancy-associated glycoproteins and late embryonic mortality in lactating dairy herds. Journal of Dairy Science, 99(2), 1584-1594. https://doi.org/10.3168/jds.2015-10192
Sugino, N., & Okuda, K. (2007). Species-related differences in the mechanism of apoptosis during structural luteolysis. Journal of Reproduction and Development, 53(5), 977-986. https://doi.org/10.1262/jrd.19047
Swarup, V., & Rajeswari, M. R. (2007). Circulating (cell-free) nucleic acids-A promising, non-invasive tool for early detection of several human diseases. FEBS Letters, 581(5), 795-799. https://doi.org/10.1016/j.febslet.2007.01.051