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Rhodamine-marked bombesin: a novel means for prostate cancer fluorescence imaging
Summary The gastrin releasing peptide receptor (GRPR) has been found to be strongly expressed in various types of cancers such as prostate and breast carcinomas. The GRPR ligands gastrin releasing peptide and bombesin can play a very significant role in cancer therapy and diagnostics. In this study...
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Published in: | Investigational new drugs 2014-02, Vol.32 (1), p.37-46 |
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description | Summary
The gastrin releasing peptide receptor (GRPR) has been found to be strongly expressed in various types of cancers such as prostate and breast carcinomas. The GRPR ligands gastrin releasing peptide and bombesin can play a very significant role in cancer therapy and diagnostics. In this study we synthesized unlabeled bombesin BBN along with two conjugates in which the correct bombesin (BBN-Rhd) and a mutant bombesin (mBBN-Rhd) sequence was coupled to rhodamine, a fluorescent dye. These novel rhodamine fluorescent conjugates were used to study the targeting and uptake of bombesin on a cellular level. Nine different human cell lines including both tumor and healthy cells were examined using flow cytometry and confocal laser scanning microscopy. GRPR mRNA expression analysis was performed and it was found that the receptor is highly expressed in LNCaP and PC3 cells compared to the rest of other cell lines. Competition experiments were performed to verify the receptor dependence of the labeled conjugates using unmarked bombesin. The present study is a first attempt at direct fluorescence imaging of living cells using bombesin and its target, the GRPR. A rhodamine bombesin conjugate can be used as marker to differentiate between healthy cells and malignant cells such as prostate hyperplasia and prostate carcinoma in the early detection of cancer. |
doi_str_mv | 10.1007/s10637-013-9975-2 |
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The gastrin releasing peptide receptor (GRPR) has been found to be strongly expressed in various types of cancers such as prostate and breast carcinomas. The GRPR ligands gastrin releasing peptide and bombesin can play a very significant role in cancer therapy and diagnostics. In this study we synthesized unlabeled bombesin BBN along with two conjugates in which the correct bombesin (BBN-Rhd) and a mutant bombesin (mBBN-Rhd) sequence was coupled to rhodamine, a fluorescent dye. These novel rhodamine fluorescent conjugates were used to study the targeting and uptake of bombesin on a cellular level. Nine different human cell lines including both tumor and healthy cells were examined using flow cytometry and confocal laser scanning microscopy. GRPR mRNA expression analysis was performed and it was found that the receptor is highly expressed in LNCaP and PC3 cells compared to the rest of other cell lines. Competition experiments were performed to verify the receptor dependence of the labeled conjugates using unmarked bombesin. The present study is a first attempt at direct fluorescence imaging of living cells using bombesin and its target, the GRPR. A rhodamine bombesin conjugate can be used as marker to differentiate between healthy cells and malignant cells such as prostate hyperplasia and prostate carcinoma in the early detection of cancer.</description><identifier>ISSN: 0167-6997</identifier><identifier>EISSN: 1573-0646</identifier><identifier>DOI: 10.1007/s10637-013-9975-2</identifier><identifier>PMID: 23728918</identifier><identifier>CODEN: INNDDK</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Amino Acid Sequence ; Antineoplastic agents ; Biological and medical sciences ; Bombesin - chemistry ; Cancer therapies ; Cell Line, Tumor ; Cell Survival ; Clinical trials ; Diagnostic Imaging ; Flow Cytometry ; Fluorescence ; Fluorescent Dyes ; Gene Expression Regulation, Neoplastic ; Gynecology. Andrology. Obstetrics ; Humans ; Hyperplasia ; Immunoassay ; Investigations ; Laboratories ; Ligands ; Male ; Male genital diseases ; Mammals ; Medical sciences ; Medicine ; Medicine & Public Health ; Microscopy ; Molecular Sequence Data ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Nephrology. Urinary tract diseases ; Oncology ; Peptides ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Preclinical Studies ; Prostate cancer ; Prostatic Neoplasms - pathology ; Receptors, Bombesin - metabolism ; Rhodamines - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Scientific imaging ; Spectrometry, Mass, Electrospray Ionization ; Studies ; Tumors ; Tumors of the urinary system ; Urinary tract. Prostate gland</subject><ispartof>Investigational new drugs, 2014-02, Vol.32 (1), p.37-46</ispartof><rights>Springer Science+Business Media New York 2013</rights><rights>2015 INIST-CNRS</rights><rights>Springer Science+Business Media New York 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-b31641d7dfadc7778fc4c966a3b4c0c5cff1580007c09397949606bea587cc0e3</citedby><cites>FETCH-LOGICAL-c402t-b31641d7dfadc7778fc4c966a3b4c0c5cff1580007c09397949606bea587cc0e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1494265495/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1494265495?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,11668,27903,27904,36039,36040,44342,74642</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28260288$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23728918$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sturzu, Alexander</creatorcontrib><creatorcontrib>Sheikh, Sumbla</creatorcontrib><creatorcontrib>Echner, Hartmut</creatorcontrib><creatorcontrib>Nägele, Thomas</creatorcontrib><creatorcontrib>Deeg, Martin</creatorcontrib><creatorcontrib>Amin, Bushra</creatorcontrib><creatorcontrib>Schwentner, Christian</creatorcontrib><creatorcontrib>Horger, Marius</creatorcontrib><creatorcontrib>Ernemann, Ulrike</creatorcontrib><creatorcontrib>Heckl, Stefan</creatorcontrib><title>Rhodamine-marked bombesin: a novel means for prostate cancer fluorescence imaging</title><title>Investigational new drugs</title><addtitle>Invest New Drugs</addtitle><addtitle>Invest New Drugs</addtitle><description>Summary
The gastrin releasing peptide receptor (GRPR) has been found to be strongly expressed in various types of cancers such as prostate and breast carcinomas. The GRPR ligands gastrin releasing peptide and bombesin can play a very significant role in cancer therapy and diagnostics. In this study we synthesized unlabeled bombesin BBN along with two conjugates in which the correct bombesin (BBN-Rhd) and a mutant bombesin (mBBN-Rhd) sequence was coupled to rhodamine, a fluorescent dye. These novel rhodamine fluorescent conjugates were used to study the targeting and uptake of bombesin on a cellular level. Nine different human cell lines including both tumor and healthy cells were examined using flow cytometry and confocal laser scanning microscopy. GRPR mRNA expression analysis was performed and it was found that the receptor is highly expressed in LNCaP and PC3 cells compared to the rest of other cell lines. Competition experiments were performed to verify the receptor dependence of the labeled conjugates using unmarked bombesin. The present study is a first attempt at direct fluorescence imaging of living cells using bombesin and its target, the GRPR. A rhodamine bombesin conjugate can be used as marker to differentiate between healthy cells and malignant cells such as prostate hyperplasia and prostate carcinoma in the early detection of cancer.</description><subject>Amino Acid Sequence</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Bombesin - chemistry</subject><subject>Cancer therapies</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival</subject><subject>Clinical trials</subject><subject>Diagnostic Imaging</subject><subject>Flow Cytometry</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Immunoassay</subject><subject>Investigations</subject><subject>Laboratories</subject><subject>Ligands</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Mammals</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Microscopy</subject><subject>Molecular Sequence Data</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Oncology</subject><subject>Peptides</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Preclinical Studies</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Receptors, Bombesin - metabolism</subject><subject>Rhodamines - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Scientific imaging</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Studies</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. 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Andrology. Obstetrics</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Immunoassay</topic><topic>Investigations</topic><topic>Laboratories</topic><topic>Ligands</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Mammals</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Microscopy</topic><topic>Molecular Sequence Data</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Oncology</topic><topic>Peptides</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Preclinical Studies</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Receptors, Bombesin - metabolism</topic><topic>Rhodamines - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Scientific imaging</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Studies</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. 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The gastrin releasing peptide receptor (GRPR) has been found to be strongly expressed in various types of cancers such as prostate and breast carcinomas. The GRPR ligands gastrin releasing peptide and bombesin can play a very significant role in cancer therapy and diagnostics. In this study we synthesized unlabeled bombesin BBN along with two conjugates in which the correct bombesin (BBN-Rhd) and a mutant bombesin (mBBN-Rhd) sequence was coupled to rhodamine, a fluorescent dye. These novel rhodamine fluorescent conjugates were used to study the targeting and uptake of bombesin on a cellular level. Nine different human cell lines including both tumor and healthy cells were examined using flow cytometry and confocal laser scanning microscopy. GRPR mRNA expression analysis was performed and it was found that the receptor is highly expressed in LNCaP and PC3 cells compared to the rest of other cell lines. Competition experiments were performed to verify the receptor dependence of the labeled conjugates using unmarked bombesin. The present study is a first attempt at direct fluorescence imaging of living cells using bombesin and its target, the GRPR. A rhodamine bombesin conjugate can be used as marker to differentiate between healthy cells and malignant cells such as prostate hyperplasia and prostate carcinoma in the early detection of cancer.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>23728918</pmid><doi>10.1007/s10637-013-9975-2</doi><tpages>10</tpages></addata></record> |
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subjects | Amino Acid Sequence Antineoplastic agents Biological and medical sciences Bombesin - chemistry Cancer therapies Cell Line, Tumor Cell Survival Clinical trials Diagnostic Imaging Flow Cytometry Fluorescence Fluorescent Dyes Gene Expression Regulation, Neoplastic Gynecology. Andrology. Obstetrics Humans Hyperplasia Immunoassay Investigations Laboratories Ligands Male Male genital diseases Mammals Medical sciences Medicine Medicine & Public Health Microscopy Molecular Sequence Data Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Nephrology. Urinary tract diseases Oncology Peptides Pharmacology. Drug treatments Pharmacology/Toxicology Preclinical Studies Prostate cancer Prostatic Neoplasms - pathology Receptors, Bombesin - metabolism Rhodamines - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Scientific imaging Spectrometry, Mass, Electrospray Ionization Studies Tumors Tumors of the urinary system Urinary tract. Prostate gland |
title | Rhodamine-marked bombesin: a novel means for prostate cancer fluorescence imaging |
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