Matches in SemOpenAlex for { <https://semopenalex.org/work/W1541695406> ?p ?o ?g. }
- W1541695406 endingPage "1051" @default.
- W1541695406 startingPage "1041" @default.
- W1541695406 abstract "Our earlier work showed that knockout of hematopoietic prostaglandin D synthase (HPGDS, an enzyme that produces prostaglandin D2) caused more adenomas in Apc(Min/+) mice. Conversely, highly expressed transgenic HPGDS allowed fewer tumors. Prostaglandin D2 (PGD2) binds to the prostaglandin D2 receptor known as PTGDR (or DP1). PGD2 metabolites bind to peroxisome proliferator-activated receptor γ (PPARG). We hypothesized that Ptgdr or Pparg knockouts may raise numbers of tumors, if these receptors take part in tumor suppression by PGD2. To assess, we produced Apc(Min/+) mice with and without Ptgdr knockouts (147 mice). In separate experiments, we produced Apc(Min/+) mice expressing transgenic lipocalin-type prostaglandin D synthase (PTGDS), with and without heterozygous Pparg knockouts (104 mice). Homozygous Ptgdr knockouts raised total numbers of tumors by 30-40% at 6 and 14 weeks. Colon tumors were not affected. Heterozygous Pparg knockouts alone did not affect tumor numbers in Apc(Min/+) mice. As mentioned above, our Pparg knockout assessment also included mice with highly expressed PTGDS transgenes. Apc(Min/+) mice with transgenic PTGDS had fewer large adenomas (63% of control) and lower levels of v-myc avian myelocytomatosis viral oncogene homolog (MYC) mRNA in the colon. Heterozygous Pparg knockouts appeared to blunt the tumor-suppressing effect of transgenic PTGDS. However, tumor suppression by PGD2 was more clearly mediated by receptor PTGDR in our experiments. The suppression mechanism did not appear to involve changes in microvessel density or slower proliferation of tumor cells. The data support a role for PGD2 signals acting through PTGDR in suppression of intestinal tumors." @default.
- W1541695406 created "2016-06-24" @default.
- W1541695406 creator A5003758897 @default.
- W1541695406 creator A5007492080 @default.
- W1541695406 creator A5007723262 @default.
- W1541695406 creator A5014132162 @default.
- W1541695406 creator A5021079953 @default.
- W1541695406 creator A5024203592 @default.
- W1541695406 creator A5024624058 @default.
- W1541695406 creator A5033298543 @default.
- W1541695406 creator A5046223778 @default.
- W1541695406 creator A5058576929 @default.
- W1541695406 creator A5060772179 @default.
- W1541695406 creator A5066583708 @default.
- W1541695406 creator A5077744427 @default.
- W1541695406 creator A5080014406 @default.
- W1541695406 creator A5081248010 @default.
- W1541695406 date "2014-04-12" @default.
- W1541695406 modified "2023-09-27" @default.
- W1541695406 title "Intestinal tumor suppression in <i>Apc</i> <sup>Min/+</sup> mice by prostaglandin D <sub>2</sub> receptor <scp>PTGDR</scp>" @default.
- W1541695406 cites W1565847282 @default.
- W1541695406 cites W1812573520 @default.
- W1541695406 cites W1878091572 @default.
- W1541695406 cites W1966429228 @default.
- W1541695406 cites W1981062818 @default.
- W1541695406 cites W1981336118 @default.
- W1541695406 cites W1983930473 @default.
- W1541695406 cites W1983946189 @default.
- W1541695406 cites W1985336556 @default.
- W1541695406 cites W1989838345 @default.
- W1541695406 cites W1996302902 @default.
- W1541695406 cites W1996390166 @default.
- W1541695406 cites W1999183933 @default.
- W1541695406 cites W2015930054 @default.
- W1541695406 cites W2029686419 @default.
- W1541695406 cites W2030445517 @default.
- W1541695406 cites W2032870564 @default.
- W1541695406 cites W2041672953 @default.
- W1541695406 cites W2049909747 @default.
- W1541695406 cites W2055912677 @default.
- W1541695406 cites W2058172887 @default.
- W1541695406 cites W2072000048 @default.
- W1541695406 cites W2072747624 @default.
- W1541695406 cites W2090562908 @default.
- W1541695406 cites W2092040814 @default.
- W1541695406 cites W2105078414 @default.
- W1541695406 cites W2106464597 @default.
- W1541695406 cites W2115101593 @default.
- W1541695406 cites W2117254494 @default.
- W1541695406 cites W2117470642 @default.
- W1541695406 cites W2124499950 @default.
- W1541695406 cites W2130414223 @default.
- W1541695406 cites W2134359750 @default.
- W1541695406 cites W2143364414 @default.
- W1541695406 cites W2149482571 @default.
- W1541695406 cites W2153028713 @default.
- W1541695406 cites W2156783332 @default.
- W1541695406 cites W2157808707 @default.
- W1541695406 cites W2158304082 @default.
- W1541695406 cites W2166290677 @default.
- W1541695406 cites W2313793103 @default.
- W1541695406 doi "https://doi.org/10.1002/cam4.251" @default.
- W1541695406 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4303173" @default.
- W1541695406 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24729479" @default.
- W1541695406 hasPublicationYear "2014" @default.
- W1541695406 type Work @default.
- W1541695406 sameAs 1541695406 @default.
- W1541695406 citedByCount "17" @default.
- W1541695406 countsByYear W15416954062018 @default.
- W1541695406 countsByYear W15416954062019 @default.
- W1541695406 countsByYear W15416954062020 @default.
- W1541695406 countsByYear W15416954062021 @default.
- W1541695406 countsByYear W15416954062022 @default.
- W1541695406 countsByYear W15416954062023 @default.
- W1541695406 crossrefType "journal-article" @default.
- W1541695406 hasAuthorship W1541695406A5003758897 @default.
- W1541695406 hasAuthorship W1541695406A5007492080 @default.
- W1541695406 hasAuthorship W1541695406A5007723262 @default.
- W1541695406 hasAuthorship W1541695406A5014132162 @default.
- W1541695406 hasAuthorship W1541695406A5021079953 @default.
- W1541695406 hasAuthorship W1541695406A5024203592 @default.
- W1541695406 hasAuthorship W1541695406A5024624058 @default.
- W1541695406 hasAuthorship W1541695406A5033298543 @default.
- W1541695406 hasAuthorship W1541695406A5046223778 @default.
- W1541695406 hasAuthorship W1541695406A5058576929 @default.
- W1541695406 hasAuthorship W1541695406A5060772179 @default.
- W1541695406 hasAuthorship W1541695406A5066583708 @default.
- W1541695406 hasAuthorship W1541695406A5077744427 @default.
- W1541695406 hasAuthorship W1541695406A5080014406 @default.
- W1541695406 hasAuthorship W1541695406A5081248010 @default.
- W1541695406 hasBestOaLocation W15416954061 @default.
- W1541695406 hasConcept C102230213 @default.
- W1541695406 hasConcept C104317684 @default.
- W1541695406 hasConcept C126322002 @default.
- W1541695406 hasConcept C130241916 @default.
- W1541695406 hasConcept C134018914 @default.
- W1541695406 hasConcept C170493617 @default.
- W1541695406 hasConcept C182704531 @default.