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1.
PLoS One ; 18(3): e0280421, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36928065

RESUMO

A synthetic estrogen, diethylstilbestrol (DES), is known to cause adult vaginal carcinoma by neonatal administration of DES to mice. However, the carcinogenic process remains unclear. By Cap Analysis of Gene Expression method, we found that neonatal DES exposure up-regulated inflammatory Cxcl chemokines 2, 3, 5, and 7 located in the 5qE1 region in the vaginal epithelium of mice 70 days after birth. When we examined the gene expressions of these genes much earlier stages, we found that neonatal DES exposure increased these Cxcl chemokine genes expression even after 17 days after birth. It implies the DES-mediated persistent activation of inflammatory genes. Intriguingly, we also detected DES-induced non-coding RNAs from a region approximately 100 kb far from the Cxcl5 gene. The non-coding RNA up-regulation by DES exposure was confirmed on the 17-day vagina and continued throughout life, which may responsible for the activation of Cxcl chemokines located in the same region, 5qE1. This study shows that neonatal administration of DES to mice causes long-lasting up-regulation of inflammatory Cxcl chemokines in the vaginal epithelium. DES-mediated inflammation may be associated with the carcinogenic process.


Assuntos
Quimiocinas CXC , Dietilestilbestrol , Congêneres do Estradiol , Animais , Feminino , Camundongos , Animais Recém-Nascidos , Carcinógenos/farmacologia , Dietilestilbestrol/efeitos adversos , Dietilestilbestrol/farmacologia , Epitélio/patologia , Congêneres do Estradiol/efeitos adversos , Congêneres do Estradiol/farmacologia , Vagina/metabolismo , Neoplasias Vaginais/induzido quimicamente , Quimiocinas CXC/efeitos dos fármacos , Quimiocinas CXC/metabolismo
2.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-1010567

RESUMO

Vibrio parahaemolyticus is a major pathogen frequently found in seafood. Rapid and accurate detection of this pathogen is important for the control of bacterial foodborne diseases and to ensure food safety. In this study, we established a one-pot system that combines uracil-DNA glycosylase (UDG), loop-mediated isothermal amplification (LAMP), and clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 12b (Cas12b) for detecting V. parahaemolyticus in seafood. This detection system can effectively perform identification using a single tube and avoid the risk of carry-over contamination.


Assuntos
Vibrio parahaemolyticus/genética , Uracila-DNA Glicosidase/genética , Temperatura Alta , Sistemas CRISPR-Cas , Inocuidade dos Alimentos
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