Loading…
LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma
Abstract Despite clinical advances in diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains the third leading cause of cancer death, and is still associated with poor prognosis and dismal survival rates. Identifying novel PDAC-targeted tools to tackle these unmet clinical needs is...
Saved in:
Published in: | Communications biology 2021-12, Vol.4 (1) |
---|---|
Main Authors: | , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 1 |
container_start_page | |
container_title | Communications biology |
container_volume | 4 |
creator | Acier, Angélina Godard, Magali Gassiot, Fanny Finetti, Pascal Rubis, Marion Nowak, Jonathan Bertucci, François Iovanna, Juan Tomasini, Richard Lécorché, Pascaline Jacquot, Guillaume Khrestchatisky, Michel Temsamani, Jamal Malicet, Cédric Vasseur, Sophie Guillaumond, Fabienne |
description | Abstract Despite clinical advances in diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains the third leading cause of cancer death, and is still associated with poor prognosis and dismal survival rates. Identifying novel PDAC-targeted tools to tackle these unmet clinical needs is thus an urgent requirement. Here we use a peptide conjugate that specifically targets PDAC through low-density lipoprotein receptor (LDLR). We demonstrate by using near-infrared fluorescence imaging the potential of this conjugate to specifically detect and discriminate primary PDAC from healthy organs including pancreas and from benign mass-forming chronic pancreatitis, as well as detect metastatic pancreatic cancer cells in healthy liver. This work paves the way towards clinical applications in which safe LDLR-targeting peptide conjugate promotes tumor-specific delivery of imaging and/or therapeutic agents, thereby leading to substantial improvements of the PDAC patient’s outcome. |
doi_str_mv | 10.1038/s42003-021-02508-0 |
format | article |
fullrecord | <record><control><sourceid>hal</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_04235770v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_HAL_hal_04235770v1</sourcerecordid><originalsourceid>FETCH-hal_primary_oai_HAL_hal_04235770v13</originalsourceid><addsrcrecordid>eNqVijtLBDEURoMouOj-AavbWkRvktlHSvHBFlNuP1wymTHLbG5IsgP-e0ewsLX4OB-HI8SDwieFZv9cGo1oJGq1bIN7iVdipY210mwbff3n34p1KSdEVNbarWlWIrRvLWTvfKqcZVoQeg-O4-kyUvVABUKEOcwMlXmCgTOU5F0YgoNKefQ1xBF4gETRZU918f3FVZqAeh_ZUXYh8pnuxc1AU_HrX96Jx4_34-tBftLUpRzOlL86ptAdXtrux2GjzWa3w1mZ_7TfsXBTuA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central (Open access)</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Acier, Angélina ; Godard, Magali ; Gassiot, Fanny ; Finetti, Pascal ; Rubis, Marion ; Nowak, Jonathan ; Bertucci, François ; Iovanna, Juan ; Tomasini, Richard ; Lécorché, Pascaline ; Jacquot, Guillaume ; Khrestchatisky, Michel ; Temsamani, Jamal ; Malicet, Cédric ; Vasseur, Sophie ; Guillaumond, Fabienne</creator><creatorcontrib>Acier, Angélina ; Godard, Magali ; Gassiot, Fanny ; Finetti, Pascal ; Rubis, Marion ; Nowak, Jonathan ; Bertucci, François ; Iovanna, Juan ; Tomasini, Richard ; Lécorché, Pascaline ; Jacquot, Guillaume ; Khrestchatisky, Michel ; Temsamani, Jamal ; Malicet, Cédric ; Vasseur, Sophie ; Guillaumond, Fabienne</creatorcontrib><description>Abstract Despite clinical advances in diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains the third leading cause of cancer death, and is still associated with poor prognosis and dismal survival rates. Identifying novel PDAC-targeted tools to tackle these unmet clinical needs is thus an urgent requirement. Here we use a peptide conjugate that specifically targets PDAC through low-density lipoprotein receptor (LDLR). We demonstrate by using near-infrared fluorescence imaging the potential of this conjugate to specifically detect and discriminate primary PDAC from healthy organs including pancreas and from benign mass-forming chronic pancreatitis, as well as detect metastatic pancreatic cancer cells in healthy liver. This work paves the way towards clinical applications in which safe LDLR-targeting peptide conjugate promotes tumor-specific delivery of imaging and/or therapeutic agents, thereby leading to substantial improvements of the PDAC patient’s outcome.</description><identifier>ISSN: 2399-3642</identifier><identifier>EISSN: 2399-3642</identifier><identifier>DOI: 10.1038/s42003-021-02508-0</identifier><language>eng</language><publisher>Nature Publishing Group</publisher><subject>Life Sciences</subject><ispartof>Communications biology, 2021-12, Vol.4 (1)</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-2674-3123 ; 0000-0003-4797-8332 ; 0000-0003-0869-0811 ; 0000-0003-1822-2237 ; 0000-0001-7456-7315 ; 0000-0002-2339-8854 ; 0000-0002-6788-0327 ; 0000-0002-2674-3123 ; 0000-0003-4797-8332 ; 0000-0001-7456-7315 ; 0000-0003-1822-2237 ; 0000-0002-2339-8854 ; 0000-0003-0869-0811 ; 0000-0002-6788-0327</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04235770$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Acier, Angélina</creatorcontrib><creatorcontrib>Godard, Magali</creatorcontrib><creatorcontrib>Gassiot, Fanny</creatorcontrib><creatorcontrib>Finetti, Pascal</creatorcontrib><creatorcontrib>Rubis, Marion</creatorcontrib><creatorcontrib>Nowak, Jonathan</creatorcontrib><creatorcontrib>Bertucci, François</creatorcontrib><creatorcontrib>Iovanna, Juan</creatorcontrib><creatorcontrib>Tomasini, Richard</creatorcontrib><creatorcontrib>Lécorché, Pascaline</creatorcontrib><creatorcontrib>Jacquot, Guillaume</creatorcontrib><creatorcontrib>Khrestchatisky, Michel</creatorcontrib><creatorcontrib>Temsamani, Jamal</creatorcontrib><creatorcontrib>Malicet, Cédric</creatorcontrib><creatorcontrib>Vasseur, Sophie</creatorcontrib><creatorcontrib>Guillaumond, Fabienne</creatorcontrib><title>LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma</title><title>Communications biology</title><description>Abstract Despite clinical advances in diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains the third leading cause of cancer death, and is still associated with poor prognosis and dismal survival rates. Identifying novel PDAC-targeted tools to tackle these unmet clinical needs is thus an urgent requirement. Here we use a peptide conjugate that specifically targets PDAC through low-density lipoprotein receptor (LDLR). We demonstrate by using near-infrared fluorescence imaging the potential of this conjugate to specifically detect and discriminate primary PDAC from healthy organs including pancreas and from benign mass-forming chronic pancreatitis, as well as detect metastatic pancreatic cancer cells in healthy liver. This work paves the way towards clinical applications in which safe LDLR-targeting peptide conjugate promotes tumor-specific delivery of imaging and/or therapeutic agents, thereby leading to substantial improvements of the PDAC patient’s outcome.</description><subject>Life Sciences</subject><issn>2399-3642</issn><issn>2399-3642</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqVijtLBDEURoMouOj-AavbWkRvktlHSvHBFlNuP1wymTHLbG5IsgP-e0ewsLX4OB-HI8SDwieFZv9cGo1oJGq1bIN7iVdipY210mwbff3n34p1KSdEVNbarWlWIrRvLWTvfKqcZVoQeg-O4-kyUvVABUKEOcwMlXmCgTOU5F0YgoNKefQ1xBF4gETRZU918f3FVZqAeh_ZUXYh8pnuxc1AU_HrX96Jx4_34-tBftLUpRzOlL86ptAdXtrux2GjzWa3w1mZ_7TfsXBTuA</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>Acier, Angélina</creator><creator>Godard, Magali</creator><creator>Gassiot, Fanny</creator><creator>Finetti, Pascal</creator><creator>Rubis, Marion</creator><creator>Nowak, Jonathan</creator><creator>Bertucci, François</creator><creator>Iovanna, Juan</creator><creator>Tomasini, Richard</creator><creator>Lécorché, Pascaline</creator><creator>Jacquot, Guillaume</creator><creator>Khrestchatisky, Michel</creator><creator>Temsamani, Jamal</creator><creator>Malicet, Cédric</creator><creator>Vasseur, Sophie</creator><creator>Guillaumond, Fabienne</creator><general>Nature Publishing Group</general><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-2674-3123</orcidid><orcidid>https://orcid.org/0000-0003-4797-8332</orcidid><orcidid>https://orcid.org/0000-0003-0869-0811</orcidid><orcidid>https://orcid.org/0000-0003-1822-2237</orcidid><orcidid>https://orcid.org/0000-0001-7456-7315</orcidid><orcidid>https://orcid.org/0000-0002-2339-8854</orcidid><orcidid>https://orcid.org/0000-0002-6788-0327</orcidid><orcidid>https://orcid.org/0000-0002-2674-3123</orcidid><orcidid>https://orcid.org/0000-0003-4797-8332</orcidid><orcidid>https://orcid.org/0000-0001-7456-7315</orcidid><orcidid>https://orcid.org/0000-0003-1822-2237</orcidid><orcidid>https://orcid.org/0000-0002-2339-8854</orcidid><orcidid>https://orcid.org/0000-0003-0869-0811</orcidid><orcidid>https://orcid.org/0000-0002-6788-0327</orcidid></search><sort><creationdate>202112</creationdate><title>LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma</title><author>Acier, Angélina ; Godard, Magali ; Gassiot, Fanny ; Finetti, Pascal ; Rubis, Marion ; Nowak, Jonathan ; Bertucci, François ; Iovanna, Juan ; Tomasini, Richard ; Lécorché, Pascaline ; Jacquot, Guillaume ; Khrestchatisky, Michel ; Temsamani, Jamal ; Malicet, Cédric ; Vasseur, Sophie ; Guillaumond, Fabienne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_04235770v13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Life Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Acier, Angélina</creatorcontrib><creatorcontrib>Godard, Magali</creatorcontrib><creatorcontrib>Gassiot, Fanny</creatorcontrib><creatorcontrib>Finetti, Pascal</creatorcontrib><creatorcontrib>Rubis, Marion</creatorcontrib><creatorcontrib>Nowak, Jonathan</creatorcontrib><creatorcontrib>Bertucci, François</creatorcontrib><creatorcontrib>Iovanna, Juan</creatorcontrib><creatorcontrib>Tomasini, Richard</creatorcontrib><creatorcontrib>Lécorché, Pascaline</creatorcontrib><creatorcontrib>Jacquot, Guillaume</creatorcontrib><creatorcontrib>Khrestchatisky, Michel</creatorcontrib><creatorcontrib>Temsamani, Jamal</creatorcontrib><creatorcontrib>Malicet, Cédric</creatorcontrib><creatorcontrib>Vasseur, Sophie</creatorcontrib><creatorcontrib>Guillaumond, Fabienne</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Communications biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Acier, Angélina</au><au>Godard, Magali</au><au>Gassiot, Fanny</au><au>Finetti, Pascal</au><au>Rubis, Marion</au><au>Nowak, Jonathan</au><au>Bertucci, François</au><au>Iovanna, Juan</au><au>Tomasini, Richard</au><au>Lécorché, Pascaline</au><au>Jacquot, Guillaume</au><au>Khrestchatisky, Michel</au><au>Temsamani, Jamal</au><au>Malicet, Cédric</au><au>Vasseur, Sophie</au><au>Guillaumond, Fabienne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma</atitle><jtitle>Communications biology</jtitle><date>2021-12</date><risdate>2021</risdate><volume>4</volume><issue>1</issue><issn>2399-3642</issn><eissn>2399-3642</eissn><abstract>Abstract Despite clinical advances in diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains the third leading cause of cancer death, and is still associated with poor prognosis and dismal survival rates. Identifying novel PDAC-targeted tools to tackle these unmet clinical needs is thus an urgent requirement. Here we use a peptide conjugate that specifically targets PDAC through low-density lipoprotein receptor (LDLR). We demonstrate by using near-infrared fluorescence imaging the potential of this conjugate to specifically detect and discriminate primary PDAC from healthy organs including pancreas and from benign mass-forming chronic pancreatitis, as well as detect metastatic pancreatic cancer cells in healthy liver. This work paves the way towards clinical applications in which safe LDLR-targeting peptide conjugate promotes tumor-specific delivery of imaging and/or therapeutic agents, thereby leading to substantial improvements of the PDAC patient’s outcome.</abstract><pub>Nature Publishing Group</pub><doi>10.1038/s42003-021-02508-0</doi><orcidid>https://orcid.org/0000-0002-2674-3123</orcidid><orcidid>https://orcid.org/0000-0003-4797-8332</orcidid><orcidid>https://orcid.org/0000-0003-0869-0811</orcidid><orcidid>https://orcid.org/0000-0003-1822-2237</orcidid><orcidid>https://orcid.org/0000-0001-7456-7315</orcidid><orcidid>https://orcid.org/0000-0002-2339-8854</orcidid><orcidid>https://orcid.org/0000-0002-6788-0327</orcidid><orcidid>https://orcid.org/0000-0002-2674-3123</orcidid><orcidid>https://orcid.org/0000-0003-4797-8332</orcidid><orcidid>https://orcid.org/0000-0001-7456-7315</orcidid><orcidid>https://orcid.org/0000-0003-1822-2237</orcidid><orcidid>https://orcid.org/0000-0002-2339-8854</orcidid><orcidid>https://orcid.org/0000-0003-0869-0811</orcidid><orcidid>https://orcid.org/0000-0002-6788-0327</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2399-3642 |
ispartof | Communications biology, 2021-12, Vol.4 (1) |
issn | 2399-3642 2399-3642 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_04235770v1 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central (Open access); Springer Nature - nature.com Journals - Fully Open Access |
subjects | Life Sciences |
title | LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T13%3A41%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=LDL%20receptor-peptide%20conjugate%20as%20in%20vivo%20tool%20for%20specific%20targeting%20of%20pancreatic%20ductal%20adenocarcinoma&rft.jtitle=Communications%20biology&rft.au=Acier,%20Ang%C3%A9lina&rft.date=2021-12&rft.volume=4&rft.issue=1&rft.issn=2399-3642&rft.eissn=2399-3642&rft_id=info:doi/10.1038/s42003-021-02508-0&rft_dat=%3Chal%3Eoai_HAL_hal_04235770v1%3C/hal%3E%3Cgrp_id%3Ecdi_FETCH-hal_primary_oai_HAL_hal_04235770v13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |