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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
19
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pubmed:dateCreated |
2008-10-2
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pubmed:abstractText |
We performed comprehensive structure-activity relationship (SAR) studies on the peptide portion of antiproliferative factor (APF), a sialylated frizzled-8 related glycopeptide that inhibits normal bladder epithelial and urothelial carcinoma cell proliferation. Glycopeptide derivatives were synthesized by solid-phase methods using standard Fmoc chemistry and purified by RP-HPLC; all intermediate and final products were verified by HPLC-MS and NMR analyses. Antiproliferative activity of each derivative was determined by inhibition of (3)H-thymidine incorporation in primary normal human bladder epithelial cells. Structural components of the peptide segment of APF that proved to be important for biological activity included the presence of at least eight of the nine N-terminal amino acids, a negative charge in the C-terminal amino acid, a free amino group at the N-terminus, maintenance of a specific amino acid sequence in the C-terminal tail, and trans conformation for the peptide bonds. These data provide critical guidelines for optimization of structure in design of APF analogues as potential therapeutic agents.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-11295046,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-11866532,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-11993993,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-12005477,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-12847144,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-15282374,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-15465852,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-15476801,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-17030514,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-17616194,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-2005689,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-8284840,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-8284842,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-8911393,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18788730-9915446
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1520-4804
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
9
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5974-83
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pubmed:dateRevised |
2010-9-21
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pubmed:meshHeading |
pubmed-meshheading:18788730-Adolescent,
pubmed-meshheading:18788730-Amino Acid Sequence,
pubmed-meshheading:18788730-Amino Acids,
pubmed-meshheading:18788730-Cell Proliferation,
pubmed-meshheading:18788730-Chromatography, High Pressure Liquid,
pubmed-meshheading:18788730-Cystitis, Interstitial,
pubmed-meshheading:18788730-Dose-Response Relationship, Drug,
pubmed-meshheading:18788730-Epithelial Cells,
pubmed-meshheading:18788730-Glycopeptides,
pubmed-meshheading:18788730-Glycoproteins,
pubmed-meshheading:18788730-Growth Inhibitors,
pubmed-meshheading:18788730-Humans,
pubmed-meshheading:18788730-Magnetic Resonance Spectroscopy,
pubmed-meshheading:18788730-Mass Spectrometry,
pubmed-meshheading:18788730-Molecular Conformation,
pubmed-meshheading:18788730-Stereoisomerism,
pubmed-meshheading:18788730-Structure-Activity Relationship,
pubmed-meshheading:18788730-Urinary Bladder
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pubmed:year |
2008
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pubmed:articleTitle |
Structure-activity relationship studies for the peptide portion of the bladder epithelial cell antiproliferative factor from interstitial cystitis patients.
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pubmed:affiliation |
Structural Biophysics Laboratory, Center for Cancer Research, National Cancer Institute at Frederick, Frederick, Maryland 21702, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural,
Research Support, N.I.H., Intramural
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