Matches in SemOpenAlex for { <https://semopenalex.org/work/W3196291227> ?p ?o ?g. }
- W3196291227 abstract "Abstract Objective A homeostatic balance between reactive oxygen species production and the antioxidant redox system is an important component of normal pregnancy. Nuclear Factor Erythroid 2–Related Factor 2 (Nrf2) preserves cellular homeostasis by enhancing the cell's innate antioxidant status to reduce oxidative stress and inflammatory damage to the cell during pregnancy. Active Nrf2, in the nucleus of the cell, transactivates various antioxidant genes. The objective of this systematic review was to synthesize evidence on the role of Nrf2 in various adverse pregnancy outcomes (APOs). Methods We conducted a systematic review of the role of Nrf2 in pregnancy. Articles written in English, Portuguese, and Spanish were obtained from three different databases from inception until January 2021. The titles, abstracts and full text were reviewed independently by six reviewers. The quality of the included studies was assessed using a quality assessment tool developed to assess basic science and clinical studies. Nrf2 expression (gene and protein), functional contributions, and association with APOs were assessed. Results A total of 747 citations were identified; 80 were retained for full review. Most studies on Nrf2 have been carried out using placental tissues and placenta‐derived cells. Limited studies have been conducted using fetal membranes, uterus, and cervix. Nuclear translocation of Nrf2 results in transactivation of antioxidant enzymes, including glutathione peroxidase, hemeoxygenase‐1, and superoxide dismutase in gestational cells during pregnancy. This antioxidant response maintains cellular homeostasis during pregnancy. This promotes trophoblast cell survival and prevents cell death and abnormal angiogenesis in the placenta. Excessive and insufficient Nrf2 response may promote oxidative and reductive stress, respectively. This Nrf2 dysregulation has been associated with APOs including gestational diabetes mellitus, intrauterine growth restriction, reproductive toxicity, preeclampsia, and preterm birth. Conclusion Several studies have localized and reported an association between Nrf2's differential expression in reproductive tissues and the pathogenesis of APOs. However, a comprehensive functional understanding of Nrf2 in reproductive tissues is still lacking. Nrf2's activation and functions are complex, and therefore, current in vitro and in vivo studies are limited in their experimental approaches. We have identified key areas for future Nrf2 research that is needed to fill knowledge gaps." @default.
- W3196291227 created "2021-09-13" @default.
- W3196291227 creator A5001466539 @default.
- W3196291227 creator A5011479281 @default.
- W3196291227 creator A5024898223 @default.
- W3196291227 creator A5048431264 @default.
- W3196291227 creator A5051477656 @default.
- W3196291227 creator A5053762657 @default.
- W3196291227 creator A5056688421 @default.
- W3196291227 creator A5083194657 @default.
- W3196291227 date "2021-09-19" @default.
- W3196291227 modified "2023-10-03" @default.
- W3196291227 title "The role of nuclear factor erythroid 2–related factor 2 (NRF2) in normal and pathological pregnancy: A systematic review" @default.
- W3196291227 cites W1521391097 @default.
- W3196291227 cites W1569456926 @default.
- W3196291227 cites W1966796915 @default.
- W3196291227 cites W1966950939 @default.
- W3196291227 cites W1984683802 @default.
- W3196291227 cites W1992978123 @default.
- W3196291227 cites W2000211057 @default.
- W3196291227 cites W2006209846 @default.
- W3196291227 cites W2026741807 @default.
- W3196291227 cites W2033518083 @default.
- W3196291227 cites W2053320849 @default.
- W3196291227 cites W2060667338 @default.
- W3196291227 cites W2060814469 @default.
- W3196291227 cites W2062979358 @default.
- W3196291227 cites W2084301077 @default.
- W3196291227 cites W2084598323 @default.
- W3196291227 cites W2091986192 @default.
- W3196291227 cites W2104256886 @default.
- W3196291227 cites W2110832126 @default.
- W3196291227 cites W2117800935 @default.
- W3196291227 cites W2128058437 @default.
- W3196291227 cites W2129001744 @default.
- W3196291227 cites W2131127998 @default.
- W3196291227 cites W2138640388 @default.
- W3196291227 cites W2147512275 @default.
- W3196291227 cites W2159104621 @default.
- W3196291227 cites W2162954911 @default.
- W3196291227 cites W2320681446 @default.
- W3196291227 cites W2404667446 @default.
- W3196291227 cites W2415589882 @default.
- W3196291227 cites W2469696781 @default.
- W3196291227 cites W2520330777 @default.
- W3196291227 cites W2527141669 @default.
- W3196291227 cites W2533922325 @default.
- W3196291227 cites W2573588822 @default.
- W3196291227 cites W2582216571 @default.
- W3196291227 cites W2599545201 @default.
- W3196291227 cites W2610125785 @default.
- W3196291227 cites W2616618558 @default.
- W3196291227 cites W2745436247 @default.
- W3196291227 cites W2749957581 @default.
- W3196291227 cites W2766282766 @default.
- W3196291227 cites W2767485891 @default.
- W3196291227 cites W2794139372 @default.
- W3196291227 cites W2801868649 @default.
- W3196291227 cites W2804156855 @default.
- W3196291227 cites W2886845090 @default.
- W3196291227 cites W2887527191 @default.
- W3196291227 cites W2888676896 @default.
- W3196291227 cites W2903192443 @default.
- W3196291227 cites W2909195066 @default.
- W3196291227 cites W2911628530 @default.
- W3196291227 cites W2921515228 @default.
- W3196291227 cites W2922492435 @default.
- W3196291227 cites W2943314388 @default.
- W3196291227 cites W2945499541 @default.
- W3196291227 cites W2949519145 @default.
- W3196291227 cites W2950058936 @default.
- W3196291227 cites W2955074130 @default.
- W3196291227 cites W2957921458 @default.
- W3196291227 cites W3003956478 @default.
- W3196291227 cites W3008975075 @default.
- W3196291227 cites W3024047423 @default.
- W3196291227 cites W3027701411 @default.
- W3196291227 cites W3031388892 @default.
- W3196291227 cites W3080916031 @default.
- W3196291227 cites W3086636836 @default.
- W3196291227 cites W3087130802 @default.
- W3196291227 cites W3092115102 @default.
- W3196291227 cites W3092906597 @default.
- W3196291227 doi "https://doi.org/10.1111/aji.13496" @default.
- W3196291227 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34467607" @default.
- W3196291227 hasPublicationYear "2021" @default.
- W3196291227 type Work @default.
- W3196291227 sameAs 3196291227 @default.
- W3196291227 citedByCount "10" @default.
- W3196291227 countsByYear W31962912272021 @default.
- W3196291227 countsByYear W31962912272022 @default.
- W3196291227 countsByYear W31962912272023 @default.
- W3196291227 crossrefType "journal-article" @default.
- W3196291227 hasAuthorship W3196291227A5001466539 @default.
- W3196291227 hasAuthorship W3196291227A5011479281 @default.
- W3196291227 hasAuthorship W3196291227A5024898223 @default.
- W3196291227 hasAuthorship W3196291227A5048431264 @default.
- W3196291227 hasAuthorship W3196291227A5051477656 @default.
- W3196291227 hasAuthorship W3196291227A5053762657 @default.
- W3196291227 hasAuthorship W3196291227A5056688421 @default.