Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1993-5-17
pubmed:abstractText
Growth rate inhibition of subcutaneously implanted tumors results from feeding rats and athymic nude mice diets containing 1% cyclocreatine or 1%, 2%, 5%, or 10% creatine. The tumors studied included rat mammary tumors (Ac33tc in Lewis female rats and 13762A in Fischer 344 female rats), rat sarcoma MCI in Lewis male rats, and tumors resulting from the injection of two human neuroblastoma cell lines, IMR-5 and CHP-134, in athymic nude mice. Inhibition was observed regardless of the time experimental diets were administered, either at the time of tumor implantation or after the appearance of palpable tumors. For mammary tumor Ac33tc, the growth inhibition during 24 days after the implantation was approximately 50% for both 1% cyclocreatine and 1% creatine, and inhibition increased as creatine was increased from 2% to 10% of the diet. For the other rat mammary tumor (13762A), there was approximately 35% inhibition by both 1% cyclocreatine and 2% creatine. In the case of the MCI sarcoma, the inhibitory effect appeared more pronounced at earlier periods of growth, ranging from 26% to 41% for 1% cyclocreatine and from 30% to 53% for 1% creatine; there was no significant difference in growth rate between the tumors in the rats fed 1% and 5% creatine. The growth rate of tumors in athymic nude mice, produced by implantation of the human neuroblastoma IMR-5 cell line, appeared somewhat more effectively inhibited by 1% cyclocreatine than by 1% creatine, and 5% creatine feeding was most effective. For the CHP-134 cell line, 33% inhibition was observed for the 1% cyclocreatine diet and 71% for the 5% creatine diet. In several experiments, a delay in appearance of tumors was observed in animals on the experimental diets. In occasional experiments, neither additive inhibited tumor growth rate for the rat tumors or the athymic mouse tumors.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-11656156, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-1270421, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-2138706, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-2155150, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-2372768, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-2804134, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-3242600, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-3524351, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-386719, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4274152, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4279077, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4353270, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4356394, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4427195, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4708096, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-4725354, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-5035696, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-5165680, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-5334629, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-5459762, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-6091876, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-6749534, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-71759, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-7236260, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-7451436, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-761222, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-836276, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-875396, http://linkedlifedata.com/resource/pubmed/commentcorrection/8475072-938623
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
90
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3304-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:8475072-Animals, pubmed-meshheading:8475072-Antineoplastic Agents, pubmed-meshheading:8475072-Cell Division, pubmed-meshheading:8475072-Creatine, pubmed-meshheading:8475072-Creatinine, pubmed-meshheading:8475072-Diet, pubmed-meshheading:8475072-Female, pubmed-meshheading:8475072-Humans, pubmed-meshheading:8475072-Kinetics, pubmed-meshheading:8475072-Male, pubmed-meshheading:8475072-Mammary Neoplasms, Experimental, pubmed-meshheading:8475072-Mice, pubmed-meshheading:8475072-Mice, Nude, pubmed-meshheading:8475072-Neoplasm Metastasis, pubmed-meshheading:8475072-Neuroblastoma, pubmed-meshheading:8475072-Rats, pubmed-meshheading:8475072-Rats, Inbred F344, pubmed-meshheading:8475072-Rats, Inbred Lew, pubmed-meshheading:8475072-Time Factors, pubmed-meshheading:8475072-Transplantation, Heterologous
pubmed:year
1993
pubmed:articleTitle
Inhibition of rate of tumor growth by creatine and cyclocreatine.
pubmed:affiliation
Department of Biochemistry and Biophysics, Johnson Research Foundation, Philadelphia, PA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't