Noninvasive prognostic biomarker potential of quantifying the propeptides of Type XI collagen alpha‐1 chain (PRO‐C11) in patients with pancreatic ductal adenocarcinoma
Type XI collagen has been associated with tumor fibrosis and aggressiveness in patients with pancreatic ductal adenocarcinoma (PDAC). The propeptide on Type XI collagen is released into the circulation after proteolytic processing at either amino acid 253 or 511. This allows for a noninvasive biomar...
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Veröffentlicht in: | International journal of cancer 2021-07, Vol.149 (1), p.228-238 |
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creator | Nissen, Neel Ingemann Kehlet, Stephanie Johansen, Astrid Z. Chen, Inna M. Karsdal, Morten Johansen, Julia S. Diab, Hadi M. H. Jørgensen, Lars N. Sun, Shu Manon‐Jensen, Tina He, Yi Langholm, Lasse Willumsen, Nicholas |
description | Type XI collagen has been associated with tumor fibrosis and aggressiveness in patients with pancreatic ductal adenocarcinoma (PDAC). The propeptide on Type XI collagen is released into the circulation after proteolytic processing at either amino acid 253 or 511. This allows for a noninvasive biomarker approach to quantify Type XI collagen production. We developed two ELISA‐based biomarkers, targeting the two enzymatic cleavage sites (PRO‐C11‐253 and PRO‐C11‐511). In a discovery cohort including serum from patients with PDAC (n = 39, Stages 1‐4), chronic pancreatitis (CP, n = 12) and healthy controls (n = 20), PRO‐C11‐511, but not PRO‐C11‐253, was significantly upregulated in patients with PDAC and CP compared to healthy controls. Furthermore, PRO‐C11‐511 levels >75th percentile were associated with poor overall survival (OS) (HR, 95% CI: 3.40, 1.48‐7.83). The PRO‐C11‐511 biomarker potential was validated in serum from 686 patients with PDAC. Again, high levels of PRO‐C11‐511 (>75th percentile) were associated with poor OS (HR, 95% CI: 1.68, 1.40‐2.02). Furthermore, PRO‐C11‐511 remained significant after adjusting for clinical risk factors (HR, 95% CI: 1.50, 1.22‐1.86). In conclusion, quantifying serum levels of Type XI collagen with PRO‐C11‐511 predicts poor OS in patients with PDAC. This supports that Type XI collagen is important for PDAC biology and that PRO‐C11‐511 has prognostic noninvasive biomarker potential for patients with PDAC.
What's new?
Desmoplasia, characterized by increased collagen turnover, plays an important role in pancreatic ductal adenocarcinoma (PDAC), potentially influencing cancer progression and limiting drug uptake. Poor therapeutic response in particular appears to be associated with type XI collagen, which enters the circulation following proteolytic processing. Here, assays were developed to detect either of two type XI collagen proteolytic products, PRO‐C11‐253 or PRO‐C11‐511, in PDAC patient serum. The assays show that PRO‐C11‐511 type XI collagen is significantly upregulated in PDAC patients and is associated with poor overall survival. The findings identify a potential role for collagen products as predictive markers in PDAC. |
doi_str_mv | 10.1002/ijc.33551 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_33687786</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2524365849</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3881-a6732aa8395c02157b13b7ed64391d4b8aca1299e4af2f82d93c22bdb66e0be83</originalsourceid><addsrcrecordid>eNqNkc1u1DAQxy0EokvhwAsgS1xaoW39kTjOEUV8LKooQkXiFjnOZNdL1k5jp9XeeATeg7fiSZjtLj0gIXGyR_Obmf_Mn5DnnJ1xxsS5W9szKfOcPyAzzspizgTPH5IZ5ti84FIdkScxrhnjPGfZY3IkpdJFodWM_PwYvPM3JroboMMYlj7E5CxtXNiY8RuMdAgJfHKmp6Gj15PBf7d1fknT6q5igCG5FuIufbUdgH5dUBv63izBU9MPK_Pr-w9O7co4T08-fb7EsOL8lGI4mOSweaS3Lq0w8nYEsxvfTjbhRNOCD9aM1nmU85Q86kwf4dnhPSZf3r65qt7PLy7fLarXF3MrteZzowopjNGyzO3uEEXDZVNAqzJZ8jZrtLGGi7KEzHSi06ItpRWiaRulgDWg5TE52ffF7a4niKneuGgBV_IQpliLrCylVqIQiL78C12HafSorha5yKTKdVYidbqn7BhiHKGrh9Hhebc1Z_XOwRodrO8cRPbFoePUbKC9J_9YhoDeA7fQhC5aPKCFe4wxpiTnhRD4Y7xyCe8ZfBUmn7D01f-XIn1-oF0P239Lrhcfqr323wcJyXo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2524365849</pqid></control><display><type>article</type><title>Noninvasive prognostic biomarker potential of quantifying the propeptides of Type XI collagen alpha‐1 chain (PRO‐C11) in patients with pancreatic ductal adenocarcinoma</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Access via Wiley Online Library</source><source>Web of Science - Science Citation Index Expanded - 2021<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" /></source><creator>Nissen, Neel Ingemann ; Kehlet, Stephanie ; Johansen, Astrid Z. ; Chen, Inna M. ; Karsdal, Morten ; Johansen, Julia S. ; Diab, Hadi M. H. ; Jørgensen, Lars N. ; Sun, Shu ; Manon‐Jensen, Tina ; He, Yi ; Langholm, Lasse ; Willumsen, Nicholas</creator><creatorcontrib>Nissen, Neel Ingemann ; Kehlet, Stephanie ; Johansen, Astrid Z. ; Chen, Inna M. ; Karsdal, Morten ; Johansen, Julia S. ; Diab, Hadi M. H. ; Jørgensen, Lars N. ; Sun, Shu ; Manon‐Jensen, Tina ; He, Yi ; Langholm, Lasse ; Willumsen, Nicholas</creatorcontrib><description>Type XI collagen has been associated with tumor fibrosis and aggressiveness in patients with pancreatic ductal adenocarcinoma (PDAC). The propeptide on Type XI collagen is released into the circulation after proteolytic processing at either amino acid 253 or 511. This allows for a noninvasive biomarker approach to quantify Type XI collagen production. We developed two ELISA‐based biomarkers, targeting the two enzymatic cleavage sites (PRO‐C11‐253 and PRO‐C11‐511). In a discovery cohort including serum from patients with PDAC (n = 39, Stages 1‐4), chronic pancreatitis (CP, n = 12) and healthy controls (n = 20), PRO‐C11‐511, but not PRO‐C11‐253, was significantly upregulated in patients with PDAC and CP compared to healthy controls. Furthermore, PRO‐C11‐511 levels >75th percentile were associated with poor overall survival (OS) (HR, 95% CI: 3.40, 1.48‐7.83). The PRO‐C11‐511 biomarker potential was validated in serum from 686 patients with PDAC. Again, high levels of PRO‐C11‐511 (>75th percentile) were associated with poor OS (HR, 95% CI: 1.68, 1.40‐2.02). Furthermore, PRO‐C11‐511 remained significant after adjusting for clinical risk factors (HR, 95% CI: 1.50, 1.22‐1.86). In conclusion, quantifying serum levels of Type XI collagen with PRO‐C11‐511 predicts poor OS in patients with PDAC. This supports that Type XI collagen is important for PDAC biology and that PRO‐C11‐511 has prognostic noninvasive biomarker potential for patients with PDAC.
What's new?
Desmoplasia, characterized by increased collagen turnover, plays an important role in pancreatic ductal adenocarcinoma (PDAC), potentially influencing cancer progression and limiting drug uptake. Poor therapeutic response in particular appears to be associated with type XI collagen, which enters the circulation following proteolytic processing. Here, assays were developed to detect either of two type XI collagen proteolytic products, PRO‐C11‐253 or PRO‐C11‐511, in PDAC patient serum. The assays show that PRO‐C11‐511 type XI collagen is significantly upregulated in PDAC patients and is associated with poor overall survival. The findings identify a potential role for collagen products as predictive markers in PDAC.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.33551</identifier><identifier>PMID: 33687786</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Adenocarcinoma ; Aged ; Amino acids ; Biomarkers ; Biomarkers, Tumor - blood ; Cancer ; Carcinoma, Pancreatic Ductal - blood ; Carcinoma, Pancreatic Ductal - diagnosis ; Case-Control Studies ; Collagen ; Collagen (type I) ; Collagen Type XI - metabolism ; extracellular matrix ; Female ; Fibrosis ; Follow-Up Studies ; Humans ; Life Sciences & Biomedicine ; Male ; Medical research ; Middle Aged ; Oncology ; Pancreas ; Pancreatic cancer ; pancreatic ductal carcinoma ; Pancreatic Neoplasms ; Pancreatic Neoplasms - blood ; Pancreatic Neoplasms - diagnosis ; Pancreatitis ; Peptide Fragments - blood ; Prognosis ; Proteolysis ; Retrospective Studies ; Risk factors ; Science & Technology ; Serum levels ; Survival Rate ; tumor fibrosis</subject><ispartof>International journal of cancer, 2021-07, Vol.149 (1), p.228-238</ispartof><rights>2021 UICC</rights><rights>2021 UICC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>18</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000631172200001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c3881-a6732aa8395c02157b13b7ed64391d4b8aca1299e4af2f82d93c22bdb66e0be83</citedby><cites>FETCH-LOGICAL-c3881-a6732aa8395c02157b13b7ed64391d4b8aca1299e4af2f82d93c22bdb66e0be83</cites><orcidid>0000-0002-8970-8798 ; 0000-0002-5207-5173 ; 0000-0003-2891-0762 ; 0000-0001-5026-8740 ; 0000-0003-0549-5797</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.33551$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.33551$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,39263,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33687786$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nissen, Neel Ingemann</creatorcontrib><creatorcontrib>Kehlet, Stephanie</creatorcontrib><creatorcontrib>Johansen, Astrid Z.</creatorcontrib><creatorcontrib>Chen, Inna M.</creatorcontrib><creatorcontrib>Karsdal, Morten</creatorcontrib><creatorcontrib>Johansen, Julia S.</creatorcontrib><creatorcontrib>Diab, Hadi M. H.</creatorcontrib><creatorcontrib>Jørgensen, Lars N.</creatorcontrib><creatorcontrib>Sun, Shu</creatorcontrib><creatorcontrib>Manon‐Jensen, Tina</creatorcontrib><creatorcontrib>He, Yi</creatorcontrib><creatorcontrib>Langholm, Lasse</creatorcontrib><creatorcontrib>Willumsen, Nicholas</creatorcontrib><title>Noninvasive prognostic biomarker potential of quantifying the propeptides of Type XI collagen alpha‐1 chain (PRO‐C11) in patients with pancreatic ductal adenocarcinoma</title><title>International journal of cancer</title><addtitle>INT J CANCER</addtitle><addtitle>Int J Cancer</addtitle><description>Type XI collagen has been associated with tumor fibrosis and aggressiveness in patients with pancreatic ductal adenocarcinoma (PDAC). The propeptide on Type XI collagen is released into the circulation after proteolytic processing at either amino acid 253 or 511. This allows for a noninvasive biomarker approach to quantify Type XI collagen production. We developed two ELISA‐based biomarkers, targeting the two enzymatic cleavage sites (PRO‐C11‐253 and PRO‐C11‐511). In a discovery cohort including serum from patients with PDAC (n = 39, Stages 1‐4), chronic pancreatitis (CP, n = 12) and healthy controls (n = 20), PRO‐C11‐511, but not PRO‐C11‐253, was significantly upregulated in patients with PDAC and CP compared to healthy controls. Furthermore, PRO‐C11‐511 levels >75th percentile were associated with poor overall survival (OS) (HR, 95% CI: 3.40, 1.48‐7.83). The PRO‐C11‐511 biomarker potential was validated in serum from 686 patients with PDAC. Again, high levels of PRO‐C11‐511 (>75th percentile) were associated with poor OS (HR, 95% CI: 1.68, 1.40‐2.02). Furthermore, PRO‐C11‐511 remained significant after adjusting for clinical risk factors (HR, 95% CI: 1.50, 1.22‐1.86). In conclusion, quantifying serum levels of Type XI collagen with PRO‐C11‐511 predicts poor OS in patients with PDAC. This supports that Type XI collagen is important for PDAC biology and that PRO‐C11‐511 has prognostic noninvasive biomarker potential for patients with PDAC.
What's new?
Desmoplasia, characterized by increased collagen turnover, plays an important role in pancreatic ductal adenocarcinoma (PDAC), potentially influencing cancer progression and limiting drug uptake. Poor therapeutic response in particular appears to be associated with type XI collagen, which enters the circulation following proteolytic processing. Here, assays were developed to detect either of two type XI collagen proteolytic products, PRO‐C11‐253 or PRO‐C11‐511, in PDAC patient serum. The assays show that PRO‐C11‐511 type XI collagen is significantly upregulated in PDAC patients and is associated with poor overall survival. The findings identify a potential role for collagen products as predictive markers in PDAC.</description><subject>Adenocarcinoma</subject><subject>Aged</subject><subject>Amino acids</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - blood</subject><subject>Cancer</subject><subject>Carcinoma, Pancreatic Ductal - blood</subject><subject>Carcinoma, Pancreatic Ductal - diagnosis</subject><subject>Case-Control Studies</subject><subject>Collagen</subject><subject>Collagen (type I)</subject><subject>Collagen Type XI - metabolism</subject><subject>extracellular matrix</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Life Sciences & Biomedicine</subject><subject>Male</subject><subject>Medical research</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Pancreas</subject><subject>Pancreatic cancer</subject><subject>pancreatic ductal carcinoma</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - blood</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatitis</subject><subject>Peptide Fragments - blood</subject><subject>Prognosis</subject><subject>Proteolysis</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Science & Technology</subject><subject>Serum levels</subject><subject>Survival Rate</subject><subject>tumor fibrosis</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAQxy0EokvhwAsgS1xaoW39kTjOEUV8LKooQkXiFjnOZNdL1k5jp9XeeATeg7fiSZjtLj0gIXGyR_Obmf_Mn5DnnJ1xxsS5W9szKfOcPyAzzspizgTPH5IZ5ti84FIdkScxrhnjPGfZY3IkpdJFodWM_PwYvPM3JroboMMYlj7E5CxtXNiY8RuMdAgJfHKmp6Gj15PBf7d1fknT6q5igCG5FuIufbUdgH5dUBv63izBU9MPK_Pr-w9O7co4T08-fb7EsOL8lGI4mOSweaS3Lq0w8nYEsxvfTjbhRNOCD9aM1nmU85Q86kwf4dnhPSZf3r65qt7PLy7fLarXF3MrteZzowopjNGyzO3uEEXDZVNAqzJZ8jZrtLGGi7KEzHSi06ItpRWiaRulgDWg5TE52ffF7a4niKneuGgBV_IQpliLrCylVqIQiL78C12HafSorha5yKTKdVYidbqn7BhiHKGrh9Hhebc1Z_XOwRodrO8cRPbFoePUbKC9J_9YhoDeA7fQhC5aPKCFe4wxpiTnhRD4Y7xyCe8ZfBUmn7D01f-XIn1-oF0P239Lrhcfqr323wcJyXo</recordid><startdate>20210701</startdate><enddate>20210701</enddate><creator>Nissen, Neel Ingemann</creator><creator>Kehlet, Stephanie</creator><creator>Johansen, Astrid Z.</creator><creator>Chen, Inna M.</creator><creator>Karsdal, Morten</creator><creator>Johansen, Julia S.</creator><creator>Diab, Hadi M. H.</creator><creator>Jørgensen, Lars N.</creator><creator>Sun, Shu</creator><creator>Manon‐Jensen, Tina</creator><creator>He, Yi</creator><creator>Langholm, Lasse</creator><creator>Willumsen, Nicholas</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8970-8798</orcidid><orcidid>https://orcid.org/0000-0002-5207-5173</orcidid><orcidid>https://orcid.org/0000-0003-2891-0762</orcidid><orcidid>https://orcid.org/0000-0001-5026-8740</orcidid><orcidid>https://orcid.org/0000-0003-0549-5797</orcidid></search><sort><creationdate>20210701</creationdate><title>Noninvasive prognostic biomarker potential of quantifying the propeptides of Type XI collagen alpha‐1 chain (PRO‐C11) in patients with pancreatic ductal adenocarcinoma</title><author>Nissen, Neel Ingemann ; Kehlet, Stephanie ; Johansen, Astrid Z. ; Chen, Inna M. ; Karsdal, Morten ; Johansen, Julia S. ; Diab, Hadi M. H. ; Jørgensen, Lars N. ; Sun, Shu ; Manon‐Jensen, Tina ; He, Yi ; Langholm, Lasse ; Willumsen, Nicholas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3881-a6732aa8395c02157b13b7ed64391d4b8aca1299e4af2f82d93c22bdb66e0be83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenocarcinoma</topic><topic>Aged</topic><topic>Amino acids</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - blood</topic><topic>Cancer</topic><topic>Carcinoma, Pancreatic Ductal - blood</topic><topic>Carcinoma, Pancreatic Ductal - diagnosis</topic><topic>Case-Control Studies</topic><topic>Collagen</topic><topic>Collagen (type I)</topic><topic>Collagen Type XI - metabolism</topic><topic>extracellular matrix</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Life Sciences & Biomedicine</topic><topic>Male</topic><topic>Medical research</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Pancreas</topic><topic>Pancreatic cancer</topic><topic>pancreatic ductal carcinoma</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - blood</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatitis</topic><topic>Peptide Fragments - blood</topic><topic>Prognosis</topic><topic>Proteolysis</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Science & Technology</topic><topic>Serum levels</topic><topic>Survival Rate</topic><topic>tumor fibrosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nissen, Neel Ingemann</creatorcontrib><creatorcontrib>Kehlet, Stephanie</creatorcontrib><creatorcontrib>Johansen, Astrid Z.</creatorcontrib><creatorcontrib>Chen, Inna M.</creatorcontrib><creatorcontrib>Karsdal, Morten</creatorcontrib><creatorcontrib>Johansen, Julia S.</creatorcontrib><creatorcontrib>Diab, Hadi M. H.</creatorcontrib><creatorcontrib>Jørgensen, Lars N.</creatorcontrib><creatorcontrib>Sun, Shu</creatorcontrib><creatorcontrib>Manon‐Jensen, Tina</creatorcontrib><creatorcontrib>He, Yi</creatorcontrib><creatorcontrib>Langholm, Lasse</creatorcontrib><creatorcontrib>Willumsen, Nicholas</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nissen, Neel Ingemann</au><au>Kehlet, Stephanie</au><au>Johansen, Astrid Z.</au><au>Chen, Inna M.</au><au>Karsdal, Morten</au><au>Johansen, Julia S.</au><au>Diab, Hadi M. H.</au><au>Jørgensen, Lars N.</au><au>Sun, Shu</au><au>Manon‐Jensen, Tina</au><au>He, Yi</au><au>Langholm, Lasse</au><au>Willumsen, Nicholas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Noninvasive prognostic biomarker potential of quantifying the propeptides of Type XI collagen alpha‐1 chain (PRO‐C11) in patients with pancreatic ductal adenocarcinoma</atitle><jtitle>International journal of cancer</jtitle><stitle>INT J CANCER</stitle><addtitle>Int J Cancer</addtitle><date>2021-07-01</date><risdate>2021</risdate><volume>149</volume><issue>1</issue><spage>228</spage><epage>238</epage><pages>228-238</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><abstract>Type XI collagen has been associated with tumor fibrosis and aggressiveness in patients with pancreatic ductal adenocarcinoma (PDAC). The propeptide on Type XI collagen is released into the circulation after proteolytic processing at either amino acid 253 or 511. This allows for a noninvasive biomarker approach to quantify Type XI collagen production. We developed two ELISA‐based biomarkers, targeting the two enzymatic cleavage sites (PRO‐C11‐253 and PRO‐C11‐511). In a discovery cohort including serum from patients with PDAC (n = 39, Stages 1‐4), chronic pancreatitis (CP, n = 12) and healthy controls (n = 20), PRO‐C11‐511, but not PRO‐C11‐253, was significantly upregulated in patients with PDAC and CP compared to healthy controls. Furthermore, PRO‐C11‐511 levels >75th percentile were associated with poor overall survival (OS) (HR, 95% CI: 3.40, 1.48‐7.83). The PRO‐C11‐511 biomarker potential was validated in serum from 686 patients with PDAC. Again, high levels of PRO‐C11‐511 (>75th percentile) were associated with poor OS (HR, 95% CI: 1.68, 1.40‐2.02). Furthermore, PRO‐C11‐511 remained significant after adjusting for clinical risk factors (HR, 95% CI: 1.50, 1.22‐1.86). In conclusion, quantifying serum levels of Type XI collagen with PRO‐C11‐511 predicts poor OS in patients with PDAC. This supports that Type XI collagen is important for PDAC biology and that PRO‐C11‐511 has prognostic noninvasive biomarker potential for patients with PDAC.
What's new?
Desmoplasia, characterized by increased collagen turnover, plays an important role in pancreatic ductal adenocarcinoma (PDAC), potentially influencing cancer progression and limiting drug uptake. Poor therapeutic response in particular appears to be associated with type XI collagen, which enters the circulation following proteolytic processing. Here, assays were developed to detect either of two type XI collagen proteolytic products, PRO‐C11‐253 or PRO‐C11‐511, in PDAC patient serum. The assays show that PRO‐C11‐511 type XI collagen is significantly upregulated in PDAC patients and is associated with poor overall survival. The findings identify a potential role for collagen products as predictive markers in PDAC.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>33687786</pmid><doi>10.1002/ijc.33551</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-8970-8798</orcidid><orcidid>https://orcid.org/0000-0002-5207-5173</orcidid><orcidid>https://orcid.org/0000-0003-2891-0762</orcidid><orcidid>https://orcid.org/0000-0001-5026-8740</orcidid><orcidid>https://orcid.org/0000-0003-0549-5797</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Aged Amino acids Biomarkers Biomarkers, Tumor - blood Cancer Carcinoma, Pancreatic Ductal - blood Carcinoma, Pancreatic Ductal - diagnosis Case-Control Studies Collagen Collagen (type I) Collagen Type XI - metabolism extracellular matrix Female Fibrosis Follow-Up Studies Humans Life Sciences & Biomedicine Male Medical research Middle Aged Oncology Pancreas Pancreatic cancer pancreatic ductal carcinoma Pancreatic Neoplasms Pancreatic Neoplasms - blood Pancreatic Neoplasms - diagnosis Pancreatitis Peptide Fragments - blood Prognosis Proteolysis Retrospective Studies Risk factors Science & Technology Serum levels Survival Rate tumor fibrosis |
title | Noninvasive prognostic biomarker potential of quantifying the propeptides of Type XI collagen alpha‐1 chain (PRO‐C11) in patients with pancreatic ductal adenocarcinoma |
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