Matches in SemOpenAlex for { <https://semopenalex.org/work/W2140804547> ?p ?o ?g. }
- W2140804547 endingPage "205" @default.
- W2140804547 startingPage "195" @default.
- W2140804547 abstract "Excessive accumulation of collagen in the skin and internal organs in systemic sclerosis (SSc) is considered to result from enhanced transcription of collagen in fibroblasts. Macrolides have been reported to show various pharmacological activities. Recently, it was reported that EM703, a new derivative of erythromycin, improved bleomycin-induced pulmonary fibrosis in mice.Therefore, we attempted to examine the effects of EM703 on the type I collagen synthetic activity in normal and SSc dermal fibroblasts.Normal and SSc dermal fibroblasts were cultured with various concentrations of Erythromycin A or EM703 for 48h. Amount of type I collagen in the culture medium was measured with ELISA with anti-type I collagen antibody. Type I collagen mRNA levels were measured by northern blots analysis and type I collagen transcription and regulation of the human COL1A1 promoter activity were examined by transient transfection and luciferase assay. Electrophoretic gel mobility shift assay was also performed for measurement of binding activities of DNA binding factors to the COL1A1 promoter.We found that EM703 reduced collagen production and the mRNA levels of alpha1(I) collagen in a dose-dependent manner in the normal fibroblasts. The transcription of COL1A1 was downregulated as detected by the luciferase assay. The downregulation was also detected using DNA containing various short lengths of the COL1A1 promoter region. EM703 did not inhibit COL1A1 transcription when the luciferase assay was performed using DNA containing the COL1A1 promoter with a short substitution mutation of the CCAAT box. Decreased production of type I collagen at the transcriptional level was also found in SSc fibroblasts treated with EM703.These results suggest that EM703 inhibits the transcription of type I collagen in both normal and SSc fibroblasts, and that the transcription is inhibited through the CCAAT box of the COL1A1 promoter." @default.
- W2140804547 created "2016-06-24" @default.
- W2140804547 creator A5003923929 @default.
- W2140804547 creator A5006486850 @default.
- W2140804547 creator A5012426828 @default.
- W2140804547 creator A5028068605 @default.
- W2140804547 creator A5045164227 @default.
- W2140804547 creator A5078878264 @default.
- W2140804547 creator A5089176517 @default.
- W2140804547 date "2008-03-01" @default.
- W2140804547 modified "2023-10-18" @default.
- W2140804547 title "EM703, the new derivative of erythromycin, inhibits transcription of type I collagen in normal and scleroderma fibroblasts" @default.
- W2140804547 cites W1482988026 @default.
- W2140804547 cites W1534816195 @default.
- W2140804547 cites W1568633060 @default.
- W2140804547 cites W1575094835 @default.
- W2140804547 cites W1595309264 @default.
- W2140804547 cites W1658244448 @default.
- W2140804547 cites W1674231565 @default.
- W2140804547 cites W1964082339 @default.
- W2140804547 cites W1964161644 @default.
- W2140804547 cites W1978361666 @default.
- W2140804547 cites W1980256058 @default.
- W2140804547 cites W1980551673 @default.
- W2140804547 cites W1983640618 @default.
- W2140804547 cites W1990935670 @default.
- W2140804547 cites W1993296447 @default.
- W2140804547 cites W2003225450 @default.
- W2140804547 cites W2012490729 @default.
- W2140804547 cites W2028921539 @default.
- W2140804547 cites W2029327578 @default.
- W2140804547 cites W2032462421 @default.
- W2140804547 cites W2041168586 @default.
- W2140804547 cites W2051747444 @default.
- W2140804547 cites W2058737062 @default.
- W2140804547 cites W2060264366 @default.
- W2140804547 cites W2067136230 @default.
- W2140804547 cites W2076545156 @default.
- W2140804547 cites W2082366764 @default.
- W2140804547 cites W2089603326 @default.
- W2140804547 cites W2117322594 @default.
- W2140804547 cites W2117388663 @default.
- W2140804547 cites W2118537373 @default.
- W2140804547 cites W2119380694 @default.
- W2140804547 cites W2133070939 @default.
- W2140804547 cites W2138885527 @default.
- W2140804547 cites W2142546321 @default.
- W2140804547 cites W2145059527 @default.
- W2140804547 cites W2168476587 @default.
- W2140804547 cites W2394769977 @default.
- W2140804547 cites W41751146 @default.
- W2140804547 cites W2038201261 @default.
- W2140804547 doi "https://doi.org/10.1016/j.jdermsci.2007.10.006" @default.
- W2140804547 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18036782" @default.
- W2140804547 hasPublicationYear "2008" @default.
- W2140804547 type Work @default.
- W2140804547 sameAs 2140804547 @default.
- W2140804547 citedByCount "16" @default.
- W2140804547 countsByYear W21408045472012 @default.
- W2140804547 countsByYear W21408045472014 @default.
- W2140804547 countsByYear W21408045472016 @default.
- W2140804547 countsByYear W21408045472020 @default.
- W2140804547 countsByYear W21408045472021 @default.
- W2140804547 countsByYear W21408045472022 @default.
- W2140804547 crossrefType "journal-article" @default.
- W2140804547 hasAuthorship W2140804547A5003923929 @default.
- W2140804547 hasAuthorship W2140804547A5006486850 @default.
- W2140804547 hasAuthorship W2140804547A5012426828 @default.
- W2140804547 hasAuthorship W2140804547A5028068605 @default.
- W2140804547 hasAuthorship W2140804547A5045164227 @default.
- W2140804547 hasAuthorship W2140804547A5078878264 @default.
- W2140804547 hasAuthorship W2140804547A5089176517 @default.
- W2140804547 hasConcept C104317684 @default.
- W2140804547 hasConcept C111335760 @default.
- W2140804547 hasConcept C134018914 @default.
- W2140804547 hasConcept C138885662 @default.
- W2140804547 hasConcept C153911025 @default.
- W2140804547 hasConcept C179926584 @default.
- W2140804547 hasConcept C183978625 @default.
- W2140804547 hasConcept C185592680 @default.
- W2140804547 hasConcept C189165786 @default.
- W2140804547 hasConcept C202751555 @default.
- W2140804547 hasConcept C2780381497 @default.
- W2140804547 hasConcept C2780644872 @default.
- W2140804547 hasConcept C38008103 @default.
- W2140804547 hasConcept C41895202 @default.
- W2140804547 hasConcept C54009773 @default.
- W2140804547 hasConcept C55493867 @default.
- W2140804547 hasConcept C86339819 @default.
- W2140804547 hasConcept C86803240 @default.
- W2140804547 hasConceptScore W2140804547C104317684 @default.
- W2140804547 hasConceptScore W2140804547C111335760 @default.
- W2140804547 hasConceptScore W2140804547C134018914 @default.
- W2140804547 hasConceptScore W2140804547C138885662 @default.
- W2140804547 hasConceptScore W2140804547C153911025 @default.
- W2140804547 hasConceptScore W2140804547C179926584 @default.
- W2140804547 hasConceptScore W2140804547C183978625 @default.
- W2140804547 hasConceptScore W2140804547C185592680 @default.