Glycomic and Proteomic Profiling of Pancreatic Cyst Fluids Identifies Hyperfucosylated Lactosamines on the N-linked Glycans of Overexpressed Glycoproteins
Pancreatic cancer is now the fourth leading cause of cancer deaths in the United States, and it is associated with an alarmingly low 5-year survival rate of 5%. However, a patient's prognosis is considerably improved when the malignant lesions are identified at an early stage of the disease and...
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description | Pancreatic cancer is now the fourth leading cause of cancer deaths in the United States, and it is associated with an alarmingly low 5-year survival rate of 5%. However, a patient's prognosis is considerably improved when the malignant lesions are identified at an early stage of the disease and removed by surgical resection. Unfortunately, the absence of a practical screening strategy and clinical diagnostic test for identifying premalignant lesions within the pancreas often prevents early detection of pancreatic cancer. To aid in the development of a molecular screening system for early detection of the disease, we have performed glycomic and glycoproteomic profiling experiments on 21 pancreatic cyst fluid samples, including fluids from mucinous cystic neoplasms and intraductal papillary mucinous neoplasms, two types of mucinous cysts that are considered high risk to undergo malignant transformation. A total of 80 asparagine-linked (N-linked) glycans, including high mannose and complex structures, were identified. Of special interest was a series of complex N-linked glycans containing two to six fucose residues, located predominantly as substituents on β-lactosamine extensions. Following the observation of these “hyperfucosylated” glycans, bottom-up proteomics experiments utilizing a label-free quantitative approach were applied to the investigation of two sets of tryptically digested proteins derived from the cyst fluids: 1) all soluble proteins in the raw samples and 2) a subproteome of the soluble cyst fluid proteins that were selectively enriched for fucosylation through the use of surface-immobilized Aleuria aurantia lectin. A comparative analysis of these two proteomic data sets identified glycoproteins that were significantly enriched by lectin affinity. Several candidate glycoproteins that appear hyperfucosylated were identified, including triacylglycerol lipase and pancreatic α-amylase, which were 20- and 22-fold more abundant, respectively, following A. aurantia lectin enrichment. |
doi_str_mv | 10.1074/mcp.M111.015792 |
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Max ; Novotny, Milos V.</creator><creatorcontrib>Mann, Benjamin F. ; Goetz, John A. ; House, Michael G. ; Schmidt, C. Max ; Novotny, Milos V.</creatorcontrib><description>Pancreatic cancer is now the fourth leading cause of cancer deaths in the United States, and it is associated with an alarmingly low 5-year survival rate of 5%. However, a patient's prognosis is considerably improved when the malignant lesions are identified at an early stage of the disease and removed by surgical resection. Unfortunately, the absence of a practical screening strategy and clinical diagnostic test for identifying premalignant lesions within the pancreas often prevents early detection of pancreatic cancer. To aid in the development of a molecular screening system for early detection of the disease, we have performed glycomic and glycoproteomic profiling experiments on 21 pancreatic cyst fluid samples, including fluids from mucinous cystic neoplasms and intraductal papillary mucinous neoplasms, two types of mucinous cysts that are considered high risk to undergo malignant transformation. A total of 80 asparagine-linked (N-linked) glycans, including high mannose and complex structures, were identified. Of special interest was a series of complex N-linked glycans containing two to six fucose residues, located predominantly as substituents on β-lactosamine extensions. Following the observation of these “hyperfucosylated” glycans, bottom-up proteomics experiments utilizing a label-free quantitative approach were applied to the investigation of two sets of tryptically digested proteins derived from the cyst fluids: 1) all soluble proteins in the raw samples and 2) a subproteome of the soluble cyst fluid proteins that were selectively enriched for fucosylation through the use of surface-immobilized Aleuria aurantia lectin. A comparative analysis of these two proteomic data sets identified glycoproteins that were significantly enriched by lectin affinity. Several candidate glycoproteins that appear hyperfucosylated were identified, including triacylglycerol lipase and pancreatic α-amylase, which were 20- and 22-fold more abundant, respectively, following A. aurantia lectin enrichment.</description><identifier>ISSN: 1535-9476</identifier><identifier>EISSN: 1535-9484</identifier><identifier>DOI: 10.1074/mcp.M111.015792</identifier><identifier>PMID: 22393262</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; alpha-Amylases - genetics ; alpha-Amylases - metabolism ; Amino Sugars - analysis ; Amino Sugars - metabolism ; Biopsy, Fine-Needle ; Chromatography, Affinity ; Cyst Fluid - chemistry ; Cystadenoma, Mucinous - diagnosis ; Cystadenoma, Mucinous - metabolism ; Cystadenoma, Mucinous - pathology ; Early Diagnosis ; Female ; Fucose - metabolism ; Gene Expression ; Glycomics ; Glycoproteins - analysis ; Glycoproteins - genetics ; Glycoproteins - metabolism ; Humans ; Lectins ; Lipase - genetics ; Lipase - metabolism ; Male ; Middle Aged ; Pancreas - metabolism ; Pancreas - pathology ; Pancreatic Cyst - metabolism ; Pancreatic Cyst - pathology ; Pancreatic Neoplasms - diagnosis ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology ; Polysaccharides - analysis ; Proteomics</subject><ispartof>Molecular & cellular proteomics, 2012-07, Vol.11 (7), p.M111.015792-1-M111.015792-11</ispartof><rights>2012 © 2012 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2012 by The American Society for Biochemistry and Molecular Biology, Inc. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-4decf772c6233a622a5a2f59ebaf647c536e6e9e6730535c85f049f59a0ade673</citedby><cites>FETCH-LOGICAL-c513t-4decf772c6233a622a5a2f59ebaf647c536e6e9e6730535c85f049f59a0ade673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394951/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394951/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22393262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mann, Benjamin F.</creatorcontrib><creatorcontrib>Goetz, John A.</creatorcontrib><creatorcontrib>House, Michael G.</creatorcontrib><creatorcontrib>Schmidt, C. Max</creatorcontrib><creatorcontrib>Novotny, Milos V.</creatorcontrib><title>Glycomic and Proteomic Profiling of Pancreatic Cyst Fluids Identifies Hyperfucosylated Lactosamines on the N-linked Glycans of Overexpressed Glycoproteins</title><title>Molecular & cellular proteomics</title><addtitle>Mol Cell Proteomics</addtitle><description>Pancreatic cancer is now the fourth leading cause of cancer deaths in the United States, and it is associated with an alarmingly low 5-year survival rate of 5%. However, a patient's prognosis is considerably improved when the malignant lesions are identified at an early stage of the disease and removed by surgical resection. Unfortunately, the absence of a practical screening strategy and clinical diagnostic test for identifying premalignant lesions within the pancreas often prevents early detection of pancreatic cancer. To aid in the development of a molecular screening system for early detection of the disease, we have performed glycomic and glycoproteomic profiling experiments on 21 pancreatic cyst fluid samples, including fluids from mucinous cystic neoplasms and intraductal papillary mucinous neoplasms, two types of mucinous cysts that are considered high risk to undergo malignant transformation. A total of 80 asparagine-linked (N-linked) glycans, including high mannose and complex structures, were identified. Of special interest was a series of complex N-linked glycans containing two to six fucose residues, located predominantly as substituents on β-lactosamine extensions. Following the observation of these “hyperfucosylated” glycans, bottom-up proteomics experiments utilizing a label-free quantitative approach were applied to the investigation of two sets of tryptically digested proteins derived from the cyst fluids: 1) all soluble proteins in the raw samples and 2) a subproteome of the soluble cyst fluid proteins that were selectively enriched for fucosylation through the use of surface-immobilized Aleuria aurantia lectin. A comparative analysis of these two proteomic data sets identified glycoproteins that were significantly enriched by lectin affinity. Several candidate glycoproteins that appear hyperfucosylated were identified, including triacylglycerol lipase and pancreatic α-amylase, which were 20- and 22-fold more abundant, respectively, following A. aurantia lectin enrichment.</description><subject>Aged</subject><subject>alpha-Amylases - genetics</subject><subject>alpha-Amylases - metabolism</subject><subject>Amino Sugars - analysis</subject><subject>Amino Sugars - metabolism</subject><subject>Biopsy, Fine-Needle</subject><subject>Chromatography, Affinity</subject><subject>Cyst Fluid - chemistry</subject><subject>Cystadenoma, Mucinous - diagnosis</subject><subject>Cystadenoma, Mucinous - metabolism</subject><subject>Cystadenoma, Mucinous - pathology</subject><subject>Early Diagnosis</subject><subject>Female</subject><subject>Fucose - metabolism</subject><subject>Gene Expression</subject><subject>Glycomics</subject><subject>Glycoproteins - analysis</subject><subject>Glycoproteins - genetics</subject><subject>Glycoproteins - metabolism</subject><subject>Humans</subject><subject>Lectins</subject><subject>Lipase - genetics</subject><subject>Lipase - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pancreas - metabolism</subject><subject>Pancreas - pathology</subject><subject>Pancreatic Cyst - metabolism</subject><subject>Pancreatic Cyst - pathology</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Polysaccharides - analysis</subject><subject>Proteomics</subject><issn>1535-9476</issn><issn>1535-9484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1UU1v1DAUtBCIloUzN-Qjl2z9ESf1BQmt-iUttAc4W67z3BoSO9jOivwVfi1Od1nBgZOf34xnnt8g9JaSNSVtfTaYcf2JUromVLSSPUOnVHBRyfq8fn6s2-YEvUrpGyGM0Fa8RCeMcclZw07Rr6t-NmFwBmvf4bsYMjzdSmVd7_wDDhbfaW8i6Fz6mzllfNlPrkv4pgOfnXWQ8PU8QrSTCWnudYYOb7XJIenB-YIGj_Mj4M9VEfxewMVT-7RI3-4gws8xQkoHIIzLEM6n1-iF1X2CN4dzhb5eXnzZXFfb26ubzcdtZQTluao7MLZtmWkY57phTAvNrJBwr21Tt0bwBhqQ0LSclH2Yc2FJLQtBE90t3RX6sNcdp_sBOlM-FXWvxugGHWcVtFP_It49qoewU5zLWpYZVuj9QSCGHxOkrAaXDPS99hCmpChhNRdUPHmd7akmhpQi2KMNJWpJVJVE1ZKo2idaXrz7e7oj_0-EhSD3BCg72jmIKhkH3kDnIpisuuD-K_4b-V608A</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Mann, Benjamin F.</creator><creator>Goetz, John A.</creator><creator>House, Michael G.</creator><creator>Schmidt, C. 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Max ; Novotny, Milos V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-4decf772c6233a622a5a2f59ebaf647c536e6e9e6730535c85f049f59a0ade673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>alpha-Amylases - genetics</topic><topic>alpha-Amylases - metabolism</topic><topic>Amino Sugars - analysis</topic><topic>Amino Sugars - metabolism</topic><topic>Biopsy, Fine-Needle</topic><topic>Chromatography, Affinity</topic><topic>Cyst Fluid - chemistry</topic><topic>Cystadenoma, Mucinous - diagnosis</topic><topic>Cystadenoma, Mucinous - metabolism</topic><topic>Cystadenoma, Mucinous - pathology</topic><topic>Early Diagnosis</topic><topic>Female</topic><topic>Fucose - metabolism</topic><topic>Gene Expression</topic><topic>Glycomics</topic><topic>Glycoproteins - analysis</topic><topic>Glycoproteins - genetics</topic><topic>Glycoproteins - metabolism</topic><topic>Humans</topic><topic>Lectins</topic><topic>Lipase - genetics</topic><topic>Lipase - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pancreas - metabolism</topic><topic>Pancreas - pathology</topic><topic>Pancreatic Cyst - metabolism</topic><topic>Pancreatic Cyst - pathology</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Polysaccharides - analysis</topic><topic>Proteomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mann, Benjamin F.</creatorcontrib><creatorcontrib>Goetz, John A.</creatorcontrib><creatorcontrib>House, Michael G.</creatorcontrib><creatorcontrib>Schmidt, C. Max</creatorcontrib><creatorcontrib>Novotny, Milos V.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular & cellular proteomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mann, Benjamin F.</au><au>Goetz, John A.</au><au>House, Michael G.</au><au>Schmidt, C. Max</au><au>Novotny, Milos V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glycomic and Proteomic Profiling of Pancreatic Cyst Fluids Identifies Hyperfucosylated Lactosamines on the N-linked Glycans of Overexpressed Glycoproteins</atitle><jtitle>Molecular & cellular proteomics</jtitle><addtitle>Mol Cell Proteomics</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>11</volume><issue>7</issue><spage>M111.015792-1</spage><epage>M111.015792-11</epage><pages>M111.015792-1-M111.015792-11</pages><issn>1535-9476</issn><eissn>1535-9484</eissn><abstract>Pancreatic cancer is now the fourth leading cause of cancer deaths in the United States, and it is associated with an alarmingly low 5-year survival rate of 5%. However, a patient's prognosis is considerably improved when the malignant lesions are identified at an early stage of the disease and removed by surgical resection. Unfortunately, the absence of a practical screening strategy and clinical diagnostic test for identifying premalignant lesions within the pancreas often prevents early detection of pancreatic cancer. To aid in the development of a molecular screening system for early detection of the disease, we have performed glycomic and glycoproteomic profiling experiments on 21 pancreatic cyst fluid samples, including fluids from mucinous cystic neoplasms and intraductal papillary mucinous neoplasms, two types of mucinous cysts that are considered high risk to undergo malignant transformation. A total of 80 asparagine-linked (N-linked) glycans, including high mannose and complex structures, were identified. Of special interest was a series of complex N-linked glycans containing two to six fucose residues, located predominantly as substituents on β-lactosamine extensions. Following the observation of these “hyperfucosylated” glycans, bottom-up proteomics experiments utilizing a label-free quantitative approach were applied to the investigation of two sets of tryptically digested proteins derived from the cyst fluids: 1) all soluble proteins in the raw samples and 2) a subproteome of the soluble cyst fluid proteins that were selectively enriched for fucosylation through the use of surface-immobilized Aleuria aurantia lectin. A comparative analysis of these two proteomic data sets identified glycoproteins that were significantly enriched by lectin affinity. Several candidate glycoproteins that appear hyperfucosylated were identified, including triacylglycerol lipase and pancreatic α-amylase, which were 20- and 22-fold more abundant, respectively, following A. aurantia lectin enrichment.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22393262</pmid><doi>10.1074/mcp.M111.015792</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aged alpha-Amylases - genetics alpha-Amylases - metabolism Amino Sugars - analysis Amino Sugars - metabolism Biopsy, Fine-Needle Chromatography, Affinity Cyst Fluid - chemistry Cystadenoma, Mucinous - diagnosis Cystadenoma, Mucinous - metabolism Cystadenoma, Mucinous - pathology Early Diagnosis Female Fucose - metabolism Gene Expression Glycomics Glycoproteins - analysis Glycoproteins - genetics Glycoproteins - metabolism Humans Lectins Lipase - genetics Lipase - metabolism Male Middle Aged Pancreas - metabolism Pancreas - pathology Pancreatic Cyst - metabolism Pancreatic Cyst - pathology Pancreatic Neoplasms - diagnosis Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology Polysaccharides - analysis Proteomics |
title | Glycomic and Proteomic Profiling of Pancreatic Cyst Fluids Identifies Hyperfucosylated Lactosamines on the N-linked Glycans of Overexpressed Glycoproteins |
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