Current status of molecular diagnostic approaches using liquid biopsy
Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary m...
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Veröffentlicht in: | Journal of gastroenterology 2023-09, Vol.58 (9), p.834-847 |
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description | Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMN), arise through multiple steps of driver gene alterations in
KRAS
,
TP53
,
CDKN2A
,
SMAD4
, or
GNAS
. Hallmark mutations play a role in tumor initiation and progression, and their detection in bodily fluids is crucial for diagnosis. Recently, liquid biopsy has gained attention as an approach to complement pathological diagnosis, and in addition to mutation signatures in cell-free DNA, cell-free RNA, and extracellular vesicles have been investigated as potential diagnostic and prognostic markers. Integrating such molecular information to revise the diagnostic criteria for pancreatic cancer can enable a better understanding of the pathogenesis underlying inter-patient heterogeneity, such as sensitivity to chemotherapy and disease outcomes. This review discusses the current diagnostic approaches and clinical applications of genetic analysis in pancreatic cancer and diagnostic attempts by liquid biopsy and molecular analyses using pancreatic juice, duodenal fluid, and blood samples. Emerging knowledge in the rapidly advancing liquid biopsy field is promising for molecular profiling and diagnosing pancreatic diseases with significant diversity. |
doi_str_mv | 10.1007/s00535-023-02024-4 |
format | Article |
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KRAS
,
TP53
,
CDKN2A
,
SMAD4
, or
GNAS
. Hallmark mutations play a role in tumor initiation and progression, and their detection in bodily fluids is crucial for diagnosis. Recently, liquid biopsy has gained attention as an approach to complement pathological diagnosis, and in addition to mutation signatures in cell-free DNA, cell-free RNA, and extracellular vesicles have been investigated as potential diagnostic and prognostic markers. Integrating such molecular information to revise the diagnostic criteria for pancreatic cancer can enable a better understanding of the pathogenesis underlying inter-patient heterogeneity, such as sensitivity to chemotherapy and disease outcomes. This review discusses the current diagnostic approaches and clinical applications of genetic analysis in pancreatic cancer and diagnostic attempts by liquid biopsy and molecular analyses using pancreatic juice, duodenal fluid, and blood samples. Emerging knowledge in the rapidly advancing liquid biopsy field is promising for molecular profiling and diagnosing pancreatic diseases with significant diversity.</description><identifier>ISSN: 0944-1174</identifier><identifier>EISSN: 1435-5922</identifier><identifier>DOI: 10.1007/s00535-023-02024-4</identifier><identifier>PMID: 37470859</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Abdominal Surgery ; Adenocarcinoma ; Biopsy ; Cancer ; Carcinoma, Pancreatic Ductal - diagnosis ; Carcinoma, Pancreatic Ductal - genetics ; Carcinoma, Pancreatic Ductal - pathology ; Chemotherapy ; Colorectal Surgery ; Development and progression ; Diagnosis ; Early Detection of Cancer ; Gastroenterology ; Genetic analysis ; Hepatology ; Humans ; Liquid Biopsy ; Medical diagnosis ; Medicine ; Medicine & Public Health ; Mutation ; p53 Protein ; Pancreatic cancer ; Pancreatic diseases ; Pancreatic Neoplasms ; Pancreatic Neoplasms - diagnosis ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - pathology ; Pathology, Molecular ; Review ; RNA ; Smad4 protein ; Surgical Oncology ; Tumor proteins</subject><ispartof>Journal of gastroenterology, 2023-09, Vol.58 (9), p.834-847</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 Springer</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c566t-18b3897b3c18afa57dce65eaa95d992d51365b3b766ff76628ddfc4bad86a7ce3</citedby><cites>FETCH-LOGICAL-c566t-18b3897b3c18afa57dce65eaa95d992d51365b3b766ff76628ddfc4bad86a7ce3</cites><orcidid>0000-0002-6166-6848</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00535-023-02024-4$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00535-023-02024-4$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37470859$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takahashi, Kenji</creatorcontrib><creatorcontrib>Takeda, Yohei</creatorcontrib><creatorcontrib>Ono, Yusuke</creatorcontrib><creatorcontrib>Isomoto, Hajime</creatorcontrib><creatorcontrib>Mizukami, Yusuke</creatorcontrib><title>Current status of molecular diagnostic approaches using liquid biopsy</title><title>Journal of gastroenterology</title><addtitle>J Gastroenterol</addtitle><addtitle>J Gastroenterol</addtitle><description>Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMN), arise through multiple steps of driver gene alterations in
KRAS
,
TP53
,
CDKN2A
,
SMAD4
, or
GNAS
. Hallmark mutations play a role in tumor initiation and progression, and their detection in bodily fluids is crucial for diagnosis. Recently, liquid biopsy has gained attention as an approach to complement pathological diagnosis, and in addition to mutation signatures in cell-free DNA, cell-free RNA, and extracellular vesicles have been investigated as potential diagnostic and prognostic markers. Integrating such molecular information to revise the diagnostic criteria for pancreatic cancer can enable a better understanding of the pathogenesis underlying inter-patient heterogeneity, such as sensitivity to chemotherapy and disease outcomes. This review discusses the current diagnostic approaches and clinical applications of genetic analysis in pancreatic cancer and diagnostic attempts by liquid biopsy and molecular analyses using pancreatic juice, duodenal fluid, and blood samples. Emerging knowledge in the rapidly advancing liquid biopsy field is promising for molecular profiling and diagnosing pancreatic diseases with significant diversity.</description><subject>Abdominal Surgery</subject><subject>Adenocarcinoma</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Carcinoma, Pancreatic Ductal - diagnosis</subject><subject>Carcinoma, Pancreatic Ductal - genetics</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>Chemotherapy</subject><subject>Colorectal Surgery</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Early Detection of Cancer</subject><subject>Gastroenterology</subject><subject>Genetic analysis</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Liquid Biopsy</subject><subject>Medical diagnosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mutation</subject><subject>p53 Protein</subject><subject>Pancreatic cancer</subject><subject>Pancreatic diseases</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Pathology, Molecular</subject><subject>Review</subject><subject>RNA</subject><subject>Smad4 protein</subject><subject>Surgical Oncology</subject><subject>Tumor proteins</subject><issn>0944-1174</issn><issn>1435-5922</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kU1rFjEUhYMo9rX6B1zIgBs3U_OdmZWUl1qFghtdh0ySmabMJNNkIvTfe-vbDysiIQncPOckNwehtwSfEIzVx4KxYKLFlMHElLf8GdoRDiXRU_oc7XDPeUuI4kfoVSlXGBOGRfcSHTHFFe5Ev0Nn-5qzj1tTNrPV0qSxWdLsbZ1NblwwU0xlC7Yx65qTsZe-NLWEODVzuK7BNUNIa7l5jV6MZi7-zd1-jH58Pvu-_9JefDv_uj-9aK2QcmtJN7CuVwOzpDOjEcpZL4U3pheu76kThEkxsEFJOY6w0M650fLBuE4aZT07Rp8OvmsdFg_quGUz6zWHxeQbnUzQT09iuNRT-qkJ5pQRrsDhw51DTtfVl00voVg_zyb6VIumHYef5JILQN__hV6lmiP0B1SP4amE0kdqMrPXIY4JLra3pvpUSSyJxEQCdfIPCobzS7Ap-jFA_YmAHgQ2p1KyHx-aJFjfpq8P6WtIX_9OX3MQvfvzex4k93EDwA5AgaM4-fzY0n9sfwGBq7o3</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Takahashi, Kenji</creator><creator>Takeda, Yohei</creator><creator>Ono, Yusuke</creator><creator>Isomoto, Hajime</creator><creator>Mizukami, Yusuke</creator><general>Springer Nature Singapore</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6166-6848</orcidid></search><sort><creationdate>20230901</creationdate><title>Current status of molecular diagnostic approaches using liquid biopsy</title><author>Takahashi, Kenji ; Takeda, Yohei ; Ono, Yusuke ; Isomoto, Hajime ; Mizukami, Yusuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c566t-18b3897b3c18afa57dce65eaa95d992d51365b3b766ff76628ddfc4bad86a7ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abdominal Surgery</topic><topic>Adenocarcinoma</topic><topic>Biopsy</topic><topic>Cancer</topic><topic>Carcinoma, Pancreatic Ductal - diagnosis</topic><topic>Carcinoma, Pancreatic Ductal - genetics</topic><topic>Carcinoma, Pancreatic Ductal - pathology</topic><topic>Chemotherapy</topic><topic>Colorectal Surgery</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Early Detection of Cancer</topic><topic>Gastroenterology</topic><topic>Genetic analysis</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Liquid Biopsy</topic><topic>Medical diagnosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mutation</topic><topic>p53 Protein</topic><topic>Pancreatic cancer</topic><topic>Pancreatic diseases</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Pathology, Molecular</topic><topic>Review</topic><topic>RNA</topic><topic>Smad4 protein</topic><topic>Surgical Oncology</topic><topic>Tumor proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takahashi, Kenji</creatorcontrib><creatorcontrib>Takeda, Yohei</creatorcontrib><creatorcontrib>Ono, Yusuke</creatorcontrib><creatorcontrib>Isomoto, Hajime</creatorcontrib><creatorcontrib>Mizukami, Yusuke</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takahashi, Kenji</au><au>Takeda, Yohei</au><au>Ono, Yusuke</au><au>Isomoto, Hajime</au><au>Mizukami, Yusuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current status of molecular diagnostic approaches using liquid biopsy</atitle><jtitle>Journal of gastroenterology</jtitle><stitle>J Gastroenterol</stitle><addtitle>J Gastroenterol</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>58</volume><issue>9</issue><spage>834</spage><epage>847</epage><pages>834-847</pages><issn>0944-1174</issn><eissn>1435-5922</eissn><abstract>Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMN), arise through multiple steps of driver gene alterations in
KRAS
,
TP53
,
CDKN2A
,
SMAD4
, or
GNAS
. Hallmark mutations play a role in tumor initiation and progression, and their detection in bodily fluids is crucial for diagnosis. Recently, liquid biopsy has gained attention as an approach to complement pathological diagnosis, and in addition to mutation signatures in cell-free DNA, cell-free RNA, and extracellular vesicles have been investigated as potential diagnostic and prognostic markers. Integrating such molecular information to revise the diagnostic criteria for pancreatic cancer can enable a better understanding of the pathogenesis underlying inter-patient heterogeneity, such as sensitivity to chemotherapy and disease outcomes. This review discusses the current diagnostic approaches and clinical applications of genetic analysis in pancreatic cancer and diagnostic attempts by liquid biopsy and molecular analyses using pancreatic juice, duodenal fluid, and blood samples. Emerging knowledge in the rapidly advancing liquid biopsy field is promising for molecular profiling and diagnosing pancreatic diseases with significant diversity.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>37470859</pmid><doi>10.1007/s00535-023-02024-4</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6166-6848</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdominal Surgery Adenocarcinoma Biopsy Cancer Carcinoma, Pancreatic Ductal - diagnosis Carcinoma, Pancreatic Ductal - genetics Carcinoma, Pancreatic Ductal - pathology Chemotherapy Colorectal Surgery Development and progression Diagnosis Early Detection of Cancer Gastroenterology Genetic analysis Hepatology Humans Liquid Biopsy Medical diagnosis Medicine Medicine & Public Health Mutation p53 Protein Pancreatic cancer Pancreatic diseases Pancreatic Neoplasms Pancreatic Neoplasms - diagnosis Pancreatic Neoplasms - genetics Pancreatic Neoplasms - pathology Pathology, Molecular Review RNA Smad4 protein Surgical Oncology Tumor proteins |
title | Current status of molecular diagnostic approaches using liquid biopsy |
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