Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-11-17
pubmed:abstractText
7,12-dimethylbenz [a] anthracene (DMBA) administration to pubertal rats causes breast tumors and inhibits glutathione (GSH) production. Our previous results have established that oral glutamine (GLN) supplementation significantly reduced tumor development, restored the depressed GSH production, and caused a significant decrease in the circulating levels of insulinlike growth factor-1 (IGF-1). The present study was designed to investigate the involvement of the IGF-1-activated phosphatidylinositol 3 kinase (PI-3K)/Akt apoptotic signaling pathway.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/9,10-Dimethyl-1,2-benzanthracene, http://linkedlifedata.com/resource/pubmed/chemical/Akt1 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers, http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens, http://linkedlifedata.com/resource/pubmed/chemical/Glutamine, http://linkedlifedata.com/resource/pubmed/chemical/Glutathione, http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Somatomedin
pubmed:status
MEDLINE
pubmed:issn
0148-6071
pubmed:author
pubmed:issnType
Print
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
404-10
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:14621121-9,10-Dimethyl-1,2-benzanthracene, pubmed-meshheading:14621121-Adenocarcinoma, pubmed-meshheading:14621121-Administration, Oral, pubmed-meshheading:14621121-Animals, pubmed-meshheading:14621121-Apoptosis, pubmed-meshheading:14621121-Biological Markers, pubmed-meshheading:14621121-Breast Neoplasms, pubmed-meshheading:14621121-Carcinogens, pubmed-meshheading:14621121-Disease Models, Animal, pubmed-meshheading:14621121-Down-Regulation, pubmed-meshheading:14621121-Female, pubmed-meshheading:14621121-Glutamine, pubmed-meshheading:14621121-Glutathione, pubmed-meshheading:14621121-Insulin-Like Growth Factor I, pubmed-meshheading:14621121-Phosphatidylinositol 3-Kinases, pubmed-meshheading:14621121-Protein-Serine-Threonine Kinases, pubmed-meshheading:14621121-Proto-Oncogene Proteins, pubmed-meshheading:14621121-Proto-Oncogene Proteins c-akt, pubmed-meshheading:14621121-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:14621121-Rats, pubmed-meshheading:14621121-Rats, Sprague-Dawley, pubmed-meshheading:14621121-Receptors, Somatomedin, pubmed-meshheading:14621121-Signal Transduction, pubmed-meshheading:14621121-Up-Regulation, pubmed-meshheading:14621121-Women's Health
pubmed:articleTitle
Oral glutamine (AES-14) supplementation inhibits PI-3k/Akt signaling in experimental breast cancer.
pubmed:affiliation
Division of Breast Surgical Oncology, University of Arkansas for Medical Sciences, Little Rock, Arsansas 72205, USA.
pubmed:publicationType
Journal Article, Comparative Study