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Placental lncRNA Expression Is Associated With Prenatal Phthalate Exposure

Machtinger, Ronit (author)
Tel Aviv Univ, Ramat Gan & Sackler Sch Med, Sheba Med Ctr, Tel Aviv, Israel
Zhong, Jia (author)
Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY USA
Mansur, Abdallah (author)
Tel Aviv Univ, Ramat Gan & Sackler Sch Med, Sheba Med Ctr, Tel Aviv, Israel
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Adir, Michal (author)
Tel Aviv Univ, Ramat Gan & Sackler Sch Med, Sheba Med Ctr, Tel Aviv, Israel
Racowsky, Catherine (author)
Brigham & Womens Hosp, Boston, MA USA; Harvard Med Sch, Boston, MA USA
Hauser, Russ (author)
Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Boston, MA USA
Brennan, Kasey (author)
Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY USA
Karlsson, Oskar (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Karolinska Inst, Ctr Mol Med, Dept Clin Neurosci, Stockholm, Sweden
Baccarelli, Andrea A (author)
Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY USA
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 (creator_code:org_t)
2018-01-29
2018
English.
In: Toxicological Sciences. - : Oxford University Press (OUP). - 1096-6080 .- 1096-0929. ; 163:1, s. 116-122
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Phthalates are endocrine-disrupting chemicals that can cross the placenta and affect the fetal epigenome. Among various epigenetic regulators of gene expression, long noncoding RNAs (lncRNAs) are important players that may also be involved in the manifestation of endocrine-disrupting chemical toxicity. We sought to explore the association between maternal urinary phthalate metabolite concentrations and lncRNA expression in human placenta to better understand potential mechanisms through which lncRNAs participate in mediating phthalate toxicity. Ten patients with uncomplicated dichorionic diamniotic twin pregnancies at term were included in this study. Urinary (n = 10) and placenta samples (n = 20) were collected for all participants. Urinary samples were analyzed for 15 phthalate metabolites and 2 phthalate alternative metabolites. Real-time PCR arrays were used to identify and quantify 87 lncRNAs from the placental samples. We tested the Spearman correlation matrix to compare prenatal phthalate measures against placental lncRNA levels. lncRNA levels showed large variations across samples, with no significant differences in lncRNA expression within twin pairs. Mono-(carboxynonyl) phthalate demonstrated consistently strong correlations with most lncRNAs. The strongest correlation was observed between mono-hydroxyisobutyl phthalate and LOC91450 (Rspearman = 0.88, p < .001). This correlation remained significant after Bonferroni adjustment. Other strong correlations were observed between mono-isobutyl phthalate, DPP10 and HOTTIP (Rspearman = −0.91, p < .001). AIRN, DACT3.AS1, DLX6, DPP10, HOTTIP, LOC143666, and LOC91450 were strongly correlated with the greatest number of phthalate metabolites. Further studies are needed to validate these results and understand if the altered expression of lncRNAs in human placenta has clinical significance.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Public Health, Global Health, Social Medicine and Epidemiology (hsv//eng)

Keyword

imprinting genes
lncRNAs
phthalates
placenta
twins

Publication and Content Type

ref (subject category)
art (subject category)

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