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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1989-11-29
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pubmed:abstractText |
Membrane receptors for [D-Trp6]-luteinizing hormone-releasing hormone [( D-Trp6]-LH-RH), somatostatin (SS-14), and epidermal growth factor (EGF) were investigated in experimental N-nitrosobis-(2-oxopropyl)-amine (BOP)-induced pancreatic cancers of hamsters and in specimens of normal human pancreas and human pancreatic cancer obtained from autopsies. Membrane receptors for [D-Trp6]-LH-RH were absent in the pancreas of normal hamsters, but appeared after the carcinoma was induced with BOP. Binding capacity of SS-14 receptors was lower in membranes of BOP-induced pancreatic cancers than in the normal pancreas. In the BOP-induced pancreatic cancers, the receptors were also characterized following in vivo treatment of hamsters with microcapsules of the agonist [D-Trp6]-LH-RH, somatostatin analog RC-160, and the combination of both peptides, which resulted in significant tumor inhibition. Therapy with [D-Trp6]-LH-RH and RC-160, alone or in combination, decreased the binding capacity of receptors for [D-Trp6]-LH-RH, but increased Bmax for SS-14. There were no significant changes in characteristics of the EGF receptor following these therapies. Membranes from human pancreatic cancers showed binding sites for [D-Trp6]-LH-RH, but no binding was detected in normal human pancreas. The presence of receptors for LH-RH in pancreatic tumors of hamster and humans raises the intriguing possibility that LH-RH could be involved in complex interactions that contribute to the appearance of pancreatic cancer. The binding capacity of receptors for SS-14 in human pancreatic cancer membranes was lower, while Bmax for EGF was higher, as compared to normal pancreas.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens,
http://linkedlifedata.com/resource/pubmed/chemical/Gonadotropin-Releasing Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Luteinizing Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrosamines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, LHRH,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Somatotropin,
http://linkedlifedata.com/resource/pubmed/chemical/Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/Triptorelin Pamoate,
http://linkedlifedata.com/resource/pubmed/chemical/nitrosobis(2-oxopropyl)amine,
http://linkedlifedata.com/resource/pubmed/chemical/vapreotide
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pubmed:status |
MEDLINE
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pubmed:issn |
0885-3177
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
521-8
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:2573055-Adenocarcinoma,
pubmed-meshheading:2573055-Animals,
pubmed-meshheading:2573055-Antineoplastic Agents,
pubmed-meshheading:2573055-Autopsy,
pubmed-meshheading:2573055-Carcinogens,
pubmed-meshheading:2573055-Cricetinae,
pubmed-meshheading:2573055-Female,
pubmed-meshheading:2573055-Gonadotropin-Releasing Hormone,
pubmed-meshheading:2573055-Humans,
pubmed-meshheading:2573055-Luteinizing Hormone,
pubmed-meshheading:2573055-Mesocricetus,
pubmed-meshheading:2573055-Nitrosamines,
pubmed-meshheading:2573055-Pancreatic Neoplasms,
pubmed-meshheading:2573055-Receptor, Epidermal Growth Factor,
pubmed-meshheading:2573055-Receptors, LHRH,
pubmed-meshheading:2573055-Receptors, Somatotropin,
pubmed-meshheading:2573055-Somatostatin,
pubmed-meshheading:2573055-Triptorelin Pamoate
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pubmed:year |
1989
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pubmed:articleTitle |
Membrane receptors for peptides in experimental and human pancreatic cancers.
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pubmed:affiliation |
Endocrine, Polypeptide and Cancer Institute, Veterans Administration Medical Center, New Orleans, Louisiana 70146.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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