Matches in SemOpenAlex for { <https://semopenalex.org/work/W1990426099> ?p ?o ?g. }
- W1990426099 endingPage "498" @default.
- W1990426099 startingPage "491" @default.
- W1990426099 abstract "Pancreatic cancer is one of the most aggressive malignancies, with high rates of invasion and metastasis and with generally poor prognosis. We previously found that metastasis was strongly associated with the expression of growth factor receptor-bound protein 7 (Grb7), which contains a Src homology 2 (SH2) domain. In this study, we evaluated Grb7 protein as a molecular target of therapy for metastatic pancreatic cancer.Grb7 protein expression was measured by immunohistochemistry in 36 human pancreatic cancer specimens and adjacent normal pancreatic tissue. We synthesized a nonphosphorylated peptide inhibitor that binds specifically to the SH2 domain of Grb7. Intracellular signaling was assessed by immunoprecipitation and immunoblot assays in cultured human pancreatic cancer cells. Cell migration was measured with a modified Boyden chamber method. Peritoneal metastasis of the pancreatic cancer cells was measured with a mouse model. All statistical tests were two-sided.We found that 22 (61%) of 36 pancreatic cancer specimens had higher levels of Grb7 protein than their corresponding normal pancreatic tissue specimens. Grb7 expression was statistically significantly different between specimens from patients without lymph node metastasis (stage N0; two of the 10 patients) and patients with lymph node metastasis (stages N1 + N2; 20 of the 26 patients) (P = .006). The Grb7 peptide inhibitor selectively blocked the interaction between Grb7 and focal adhesion kinase and blocked the phosphorylation of Grb7 protein. In vivo Grb7 peptide inhibitor statistically significantly attenuated cell migration (for control peptide, 87.5 cells migrated, 95% confidence interval [CI] = 82.6 to 92.4 cells; for Grb7 peptide, 5.7 cells migrated, 95% CI = 2.3 to 9.0 cells; P < .001) and peritoneal metastasis of the pancreatic cancer cells in a mouse model, as assessed by the number of nodules (control = 72.6 nodules, 95% CI = 55.8 to 89.4 nodules; and for Grb7 peptide = 3.2 nodules, 95% CI = 1.6 to 4.8 nodules; P < .001, t test) and their weight (control = 4.13 g, 95% CI = 3.40 to 4.86 g; Grb7 peptide = 0.19 g, 95% CI = 0.06 to 0.32 g; P < .001, t test).The Grb7 peptide inhibitor appears to be a promising molecularly targeted therapeutic agent against metastatic pancreatic cancer." @default.
- W1990426099 created "2016-06-24" @default.
- W1990426099 creator A5019200581 @default.
- W1990426099 creator A5021568645 @default.
- W1990426099 creator A5046221788 @default.
- W1990426099 creator A5060197046 @default.
- W1990426099 creator A5066565101 @default.
- W1990426099 creator A5067647817 @default.
- W1990426099 creator A5081120943 @default.
- W1990426099 date "2006-04-05" @default.
- W1990426099 modified "2023-10-18" @default.
- W1990426099 title "Specific Peptide Ligand for Grb7 Signal Transduction Protein and Pancreatic Cancer Metastasis" @default.
- W1990426099 cites W1639582946 @default.
- W1990426099 cites W1919046869 @default.
- W1990426099 cites W1985786420 @default.
- W1990426099 cites W1987349623 @default.
- W1990426099 cites W1990353912 @default.
- W1990426099 cites W1993995347 @default.
- W1990426099 cites W1995842543 @default.
- W1990426099 cites W2002355858 @default.
- W1990426099 cites W2003008393 @default.
- W1990426099 cites W2007869203 @default.
- W1990426099 cites W2013514795 @default.
- W1990426099 cites W2015942742 @default.
- W1990426099 cites W2021397240 @default.
- W1990426099 cites W2025970479 @default.
- W1990426099 cites W2026271132 @default.
- W1990426099 cites W2028393118 @default.
- W1990426099 cites W2030753600 @default.
- W1990426099 cites W2039720575 @default.
- W1990426099 cites W2054047807 @default.
- W1990426099 cites W2054870962 @default.
- W1990426099 cites W2055519466 @default.
- W1990426099 cites W2066839011 @default.
- W1990426099 cites W2068944159 @default.
- W1990426099 cites W2071892232 @default.
- W1990426099 cites W2073426453 @default.
- W1990426099 cites W2077397396 @default.
- W1990426099 cites W2108971239 @default.
- W1990426099 cites W2141954919 @default.
- W1990426099 cites W2143291443 @default.
- W1990426099 cites W2166119177 @default.
- W1990426099 cites W2166245471 @default.
- W1990426099 cites W2249984074 @default.
- W1990426099 cites W2310034942 @default.
- W1990426099 cites W4247785462 @default.
- W1990426099 cites W4299993368 @default.
- W1990426099 doi "https://doi.org/10.1093/jnci/djj105" @default.
- W1990426099 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16595785" @default.
- W1990426099 hasPublicationYear "2006" @default.
- W1990426099 type Work @default.
- W1990426099 sameAs 1990426099 @default.
- W1990426099 citedByCount "78" @default.
- W1990426099 countsByYear W19904260992012 @default.
- W1990426099 countsByYear W19904260992013 @default.
- W1990426099 countsByYear W19904260992014 @default.
- W1990426099 countsByYear W19904260992015 @default.
- W1990426099 countsByYear W19904260992016 @default.
- W1990426099 countsByYear W19904260992017 @default.
- W1990426099 countsByYear W19904260992018 @default.
- W1990426099 countsByYear W19904260992019 @default.
- W1990426099 countsByYear W19904260992020 @default.
- W1990426099 countsByYear W19904260992022 @default.
- W1990426099 countsByYear W19904260992023 @default.
- W1990426099 crossrefType "journal-article" @default.
- W1990426099 hasAuthorship W1990426099A5019200581 @default.
- W1990426099 hasAuthorship W1990426099A5021568645 @default.
- W1990426099 hasAuthorship W1990426099A5046221788 @default.
- W1990426099 hasAuthorship W1990426099A5060197046 @default.
- W1990426099 hasAuthorship W1990426099A5066565101 @default.
- W1990426099 hasAuthorship W1990426099A5067647817 @default.
- W1990426099 hasAuthorship W1990426099A5081120943 @default.
- W1990426099 hasBestOaLocation W19904260991 @default.
- W1990426099 hasConcept C121608353 @default.
- W1990426099 hasConcept C126322002 @default.
- W1990426099 hasConcept C142724271 @default.
- W1990426099 hasConcept C204232928 @default.
- W1990426099 hasConcept C2779013556 @default.
- W1990426099 hasConcept C2780210213 @default.
- W1990426099 hasConcept C502942594 @default.
- W1990426099 hasConcept C71924100 @default.
- W1990426099 hasConcept C86803240 @default.
- W1990426099 hasConcept C96232424 @default.
- W1990426099 hasConceptScore W1990426099C121608353 @default.
- W1990426099 hasConceptScore W1990426099C126322002 @default.
- W1990426099 hasConceptScore W1990426099C142724271 @default.
- W1990426099 hasConceptScore W1990426099C204232928 @default.
- W1990426099 hasConceptScore W1990426099C2779013556 @default.
- W1990426099 hasConceptScore W1990426099C2780210213 @default.
- W1990426099 hasConceptScore W1990426099C502942594 @default.
- W1990426099 hasConceptScore W1990426099C71924100 @default.
- W1990426099 hasConceptScore W1990426099C86803240 @default.
- W1990426099 hasConceptScore W1990426099C96232424 @default.
- W1990426099 hasIssue "7" @default.
- W1990426099 hasLocation W19904260991 @default.
- W1990426099 hasLocation W19904260992 @default.
- W1990426099 hasLocation W19904260993 @default.
- W1990426099 hasOpenAccess W1990426099 @default.