Matches in SemOpenAlex for { <https://semopenalex.org/work/W2017461162> ?p ?o ?g. }
- W2017461162 endingPage "24" @default.
- W2017461162 startingPage "18" @default.
- W2017461162 abstract "To evaluate the suppressive effects of nuclear factor kappa B (NF-kappaB) inhibitors on metastasis, three agents, pentoxifylline (PTX, 0.5% in diet), N-acetyl-L-cysteine (NAC, 0.5% in diet), and aspirin (ASP, 0.5% in diet) were applied in an in vivo highly metastatic rat hepatocellular carcinoma (HCC) model in F344 male rats. Administration of NF-kappaB inhibitors for 8 weeks after induction of highly metastatic HCC by sequential treatment with diethylnitrosamine and N-nitrosomorpholine did not cause any significant change in survival rate or body weight. The incidence of HCC was 100% at week 23, regardless of treatment with NF-kappaB inhibitors. PTX, NAC, and ASP did not exert any significant effect on the development or differentiation of HCCs, although PTX tended to decrease the multiplicity of HCC. Although no lung metastasis was observed in the rats killed at the end of the period of carcinogen exposure, lung metastasis was found in 100% of animals in all the groups at the end of the experiment. Multiplicity of lung metastasis was significantly decreased by PTX and NAC, whereas ASP was without significant influence. The size of metastatic nodules was also significantly reduced in the PTX treatment group. Furthermore, the inhibitory kappa-B (IkappaB) protein level, considered to be a marker for the degree of NF-kappaB transcription, was significantly suppressed by PTX. mRNA expression in HCC for vascular cell adhesion molecule-1 (VCAM-1), which is considered to play a key role in attachment of cancer cells to the endothelium, was significantly suppressed by PTX. Among the splicing variants of VEGF, VEGF-A120, VEGF-A144, VEGF-A164, and VEGF-A188, suppressed mRNA expression of VEGF-A188 appeared to be correlated with suppression of lung metastasis formation. In conclusion, the present study demonstrated that NF-kappaB inhibitors have the potential to inhibit lung metastasis from rat HCCs in vivo, and PTX is especially promising. Its mechanism of action may involve suppression of VCAM-1 and VEGF-A188 production." @default.
- W2017461162 created "2016-06-24" @default.
- W2017461162 creator A5004431119 @default.
- W2017461162 creator A5016135291 @default.
- W2017461162 creator A5032297131 @default.
- W2017461162 creator A5053534566 @default.
- W2017461162 creator A5086822738 @default.
- W2017461162 date "2004-01-01" @default.
- W2017461162 modified "2023-10-17" @default.
- W2017461162 title "Suppression of metastasis by nuclear factor kB inhibitors in an in vivo lung metastasis model of chemically induced hepatocellular carcinoma" @default.
- W2017461162 cites W1537712767 @default.
- W2017461162 cites W1584944565 @default.
- W2017461162 cites W1598952686 @default.
- W2017461162 cites W1945689998 @default.
- W2017461162 cites W1969419107 @default.
- W2017461162 cites W1983763042 @default.
- W2017461162 cites W1989417613 @default.
- W2017461162 cites W2000208898 @default.
- W2017461162 cites W2010237936 @default.
- W2017461162 cites W2013038209 @default.
- W2017461162 cites W2041524207 @default.
- W2017461162 cites W2044692830 @default.
- W2017461162 cites W2048158801 @default.
- W2017461162 cites W2061822462 @default.
- W2017461162 cites W2064554088 @default.
- W2017461162 cites W2067092255 @default.
- W2017461162 cites W2076517048 @default.
- W2017461162 cites W2077861409 @default.
- W2017461162 cites W2086221449 @default.
- W2017461162 cites W2088545432 @default.
- W2017461162 cites W2100053618 @default.
- W2017461162 cites W2114253742 @default.
- W2017461162 cites W2118402108 @default.
- W2017461162 cites W2149098147 @default.
- W2017461162 cites W2155516654 @default.
- W2017461162 cites W2231489492 @default.
- W2017461162 cites W2314325548 @default.
- W2017461162 cites W2410383546 @default.
- W2017461162 cites W4248302985 @default.
- W2017461162 doi "https://doi.org/10.1111/j.1349-7006.2004.tb03165.x" @default.
- W2017461162 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14720322" @default.
- W2017461162 hasPublicationYear "2004" @default.
- W2017461162 type Work @default.
- W2017461162 sameAs 2017461162 @default.
- W2017461162 citedByCount "37" @default.
- W2017461162 countsByYear W20174611622012 @default.
- W2017461162 countsByYear W20174611622013 @default.
- W2017461162 countsByYear W20174611622014 @default.
- W2017461162 countsByYear W20174611622015 @default.
- W2017461162 countsByYear W20174611622016 @default.
- W2017461162 countsByYear W20174611622020 @default.
- W2017461162 countsByYear W20174611622022 @default.
- W2017461162 crossrefType "journal-article" @default.
- W2017461162 hasAuthorship W2017461162A5004431119 @default.
- W2017461162 hasAuthorship W2017461162A5016135291 @default.
- W2017461162 hasAuthorship W2017461162A5032297131 @default.
- W2017461162 hasAuthorship W2017461162A5053534566 @default.
- W2017461162 hasAuthorship W2017461162A5086822738 @default.
- W2017461162 hasConcept C114246631 @default.
- W2017461162 hasConcept C121608353 @default.
- W2017461162 hasConcept C126322002 @default.
- W2017461162 hasConcept C142724271 @default.
- W2017461162 hasConcept C150903083 @default.
- W2017461162 hasConcept C207001950 @default.
- W2017461162 hasConcept C2777714996 @default.
- W2017461162 hasConcept C2778019345 @default.
- W2017461162 hasConcept C2779013556 @default.
- W2017461162 hasConcept C2779314089 @default.
- W2017461162 hasConcept C502942594 @default.
- W2017461162 hasConcept C54355233 @default.
- W2017461162 hasConcept C71924100 @default.
- W2017461162 hasConcept C86803240 @default.
- W2017461162 hasConceptScore W2017461162C114246631 @default.
- W2017461162 hasConceptScore W2017461162C121608353 @default.
- W2017461162 hasConceptScore W2017461162C126322002 @default.
- W2017461162 hasConceptScore W2017461162C142724271 @default.
- W2017461162 hasConceptScore W2017461162C150903083 @default.
- W2017461162 hasConceptScore W2017461162C207001950 @default.
- W2017461162 hasConceptScore W2017461162C2777714996 @default.
- W2017461162 hasConceptScore W2017461162C2778019345 @default.
- W2017461162 hasConceptScore W2017461162C2779013556 @default.
- W2017461162 hasConceptScore W2017461162C2779314089 @default.
- W2017461162 hasConceptScore W2017461162C502942594 @default.
- W2017461162 hasConceptScore W2017461162C54355233 @default.
- W2017461162 hasConceptScore W2017461162C71924100 @default.
- W2017461162 hasConceptScore W2017461162C86803240 @default.
- W2017461162 hasIssue "1" @default.
- W2017461162 hasLocation W20174611621 @default.
- W2017461162 hasLocation W20174611622 @default.
- W2017461162 hasOpenAccess W2017461162 @default.
- W2017461162 hasPrimaryLocation W20174611621 @default.
- W2017461162 hasRelatedWork W1911027473 @default.
- W2017461162 hasRelatedWork W1992314595 @default.
- W2017461162 hasRelatedWork W1999157020 @default.
- W2017461162 hasRelatedWork W2035703032 @default.
- W2017461162 hasRelatedWork W2117410915 @default.
- W2017461162 hasRelatedWork W2375390396 @default.
- W2017461162 hasRelatedWork W2388153334 @default.