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Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer
In this study, we explore the dynamic process of colorectal cancer progression, emphasizing the evolution toward a more metastatic phenotype. The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular struct...
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Published in: | Cell reports (Cambridge) 2024-03, Vol.43 (3), p.113912-113912, Article 113912 |
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container_end_page | 113912 |
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container_title | Cell reports (Cambridge) |
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creator | Park, Soon Sang Lee, Young-Kyoung Choi, Yong Won Lim, Su Bin Park, So Hyun Kim, Han Ki Shin, Jun Sang Kim, Young Hwa Lee, Dong Hyun Kim, Jang-Hee Park, Tae Jun |
description | In this study, we explore the dynamic process of colorectal cancer progression, emphasizing the evolution toward a more metastatic phenotype. The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular structures to collective invasion, ultimately resulting in the development of cancer cell buddings at the invasive front. Our findings highlight the spatial correlation of this evolution with tumor cell senescence, revealing distinct types of senescent tumor cells (types I and II) that play different roles in the overall cancer progression. Type I senescent tumor cells (p16INK4A+/CXCL12+/LAMC2−/MMP7−) are identified in the collective invasion region, whereas type II senescent tumor cells (p16INK4A+/CXCL12+/LAMC2+/MMP7+), representing the final evolved form, are prominently located in the partial-EMT region. Importantly, type II senescent tumor cells associate with local invasion and lymph node metastasis in colorectal cancer, potentially affecting patient prognosis.
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•Cellular senescence is associated with gradual phenotypic transition of cancer cells•Evolutionary path of cancer cells includes two types (I and II) of senescent tumor cells•Type II senescent tumor cells express MMP7 and are associated with higher metastatic potency
Park et al. unravel the spatial heterogeneity of colorectal cancer and gradual phenotypic transition from the center to the invasive front. They demonstrated that cellular senescence is associated with this evolutional transition. Type II senescent tumor cells (p16INK4A+/LAMC2+/MMP7+) were found in the invasive front and are associated with higher metastatic potency. |
doi_str_mv | 10.1016/j.celrep.2024.113912 |
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[Display omitted]
•Cellular senescence is associated with gradual phenotypic transition of cancer cells•Evolutionary path of cancer cells includes two types (I and II) of senescent tumor cells•Type II senescent tumor cells express MMP7 and are associated with higher metastatic potency
Park et al. unravel the spatial heterogeneity of colorectal cancer and gradual phenotypic transition from the center to the invasive front. They demonstrated that cellular senescence is associated with this evolutional transition. Type II senescent tumor cells (p16INK4A+/LAMC2+/MMP7+) were found in the invasive front and are associated with higher metastatic potency.</description><identifier>ISSN: 2211-1247</identifier><identifier>EISSN: 2211-1247</identifier><identifier>DOI: 10.1016/j.celrep.2024.113912</identifier><identifier>PMID: 38446659</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>cancer buddings ; cancer evolution ; Cellular Senescence - genetics ; collective invasion ; colorectal cancer ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - pathology ; CP: Cancer ; Cyclin-Dependent Kinase Inhibitor p16 - metabolism ; Humans ; LAMC2 ; lymph node metastasis ; Matrix Metalloproteinase 7 - genetics ; MMP7 ; Phenotype ; senescent tumor cells ; spatial evolution ; spatial transcriptomics</subject><ispartof>Cell reports (Cambridge), 2024-03, Vol.43 (3), p.113912-113912, Article 113912</ispartof><rights>2024 The Author(s)</rights><rights>Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-896e8ac2c6c357b5cdb2523b28a7147c90920ab117b3637e57db1080608f6df3</citedby><cites>FETCH-LOGICAL-c474t-896e8ac2c6c357b5cdb2523b28a7147c90920ab117b3637e57db1080608f6df3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38446659$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Soon Sang</creatorcontrib><creatorcontrib>Lee, Young-Kyoung</creatorcontrib><creatorcontrib>Choi, Yong Won</creatorcontrib><creatorcontrib>Lim, Su Bin</creatorcontrib><creatorcontrib>Park, So Hyun</creatorcontrib><creatorcontrib>Kim, Han Ki</creatorcontrib><creatorcontrib>Shin, Jun Sang</creatorcontrib><creatorcontrib>Kim, Young Hwa</creatorcontrib><creatorcontrib>Lee, Dong Hyun</creatorcontrib><creatorcontrib>Kim, Jang-Hee</creatorcontrib><creatorcontrib>Park, Tae Jun</creatorcontrib><title>Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer</title><title>Cell reports (Cambridge)</title><addtitle>Cell Rep</addtitle><description>In this study, we explore the dynamic process of colorectal cancer progression, emphasizing the evolution toward a more metastatic phenotype. The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular structures to collective invasion, ultimately resulting in the development of cancer cell buddings at the invasive front. Our findings highlight the spatial correlation of this evolution with tumor cell senescence, revealing distinct types of senescent tumor cells (types I and II) that play different roles in the overall cancer progression. Type I senescent tumor cells (p16INK4A+/CXCL12+/LAMC2−/MMP7−) are identified in the collective invasion region, whereas type II senescent tumor cells (p16INK4A+/CXCL12+/LAMC2+/MMP7+), representing the final evolved form, are prominently located in the partial-EMT region. Importantly, type II senescent tumor cells associate with local invasion and lymph node metastasis in colorectal cancer, potentially affecting patient prognosis.
[Display omitted]
•Cellular senescence is associated with gradual phenotypic transition of cancer cells•Evolutionary path of cancer cells includes two types (I and II) of senescent tumor cells•Type II senescent tumor cells express MMP7 and are associated with higher metastatic potency
Park et al. unravel the spatial heterogeneity of colorectal cancer and gradual phenotypic transition from the center to the invasive front. They demonstrated that cellular senescence is associated with this evolutional transition. Type II senescent tumor cells (p16INK4A+/LAMC2+/MMP7+) were found in the invasive front and are associated with higher metastatic potency.</description><subject>cancer buddings</subject><subject>cancer evolution</subject><subject>Cellular Senescence - genetics</subject><subject>collective invasion</subject><subject>colorectal cancer</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>CP: Cancer</subject><subject>Cyclin-Dependent Kinase Inhibitor p16 - metabolism</subject><subject>Humans</subject><subject>LAMC2</subject><subject>lymph node metastasis</subject><subject>Matrix Metalloproteinase 7 - genetics</subject><subject>MMP7</subject><subject>Phenotype</subject><subject>senescent tumor cells</subject><subject>spatial evolution</subject><subject>spatial transcriptomics</subject><issn>2211-1247</issn><issn>2211-1247</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9Uctq3DAUNaGlCWn-oAQtu5mpXrbsTSAMfQQC2WQvrqXrWIPGciV5Qv6-mjoNXUUbCXEe955TVV8Y3TLKmm_7rUEfcd5yyuWWMdExflZdcM7YhnGpPvz3Pq-uUtrTchrKWCc_VeeilbJp6u6iOu7Q-8VDJAknTAYng8QlAikF4yCjJc8ujySPSNIM2YEneAx-yS5MJIdniJYAGd3TiJEcMEPKBWXIPOIU8stc1CZigg8RTS5kA8Uhfq4-DuATXr3el9Xjj--Pu1-b-4efd7vb-42RSuZN2zXYguGmMaJWfW1sz2suet6CYlKZjnacQs-Y6kUjFNbK9oy2ZdF2aOwgLqu7VdYG2Os5ugPEFx3A6b8fIT5piGVaj9p2oJSknbW0lqKv2543gxigLdqWSixaX1etOYbfC6asD67k5T1MGJakeSc5a5UUrEDlCjUxpBRxeLNmVJ_603u99qdP_em1v0K7fnVY-gPaN9K_tgrgZgVgiezoMOpk3Kkx607plqXc-w5_AN2FrnE</recordid><startdate>20240326</startdate><enddate>20240326</enddate><creator>Park, Soon Sang</creator><creator>Lee, Young-Kyoung</creator><creator>Choi, Yong Won</creator><creator>Lim, Su Bin</creator><creator>Park, So Hyun</creator><creator>Kim, Han Ki</creator><creator>Shin, Jun Sang</creator><creator>Kim, Young Hwa</creator><creator>Lee, Dong Hyun</creator><creator>Kim, Jang-Hee</creator><creator>Park, Tae Jun</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>DOA</scope></search><sort><creationdate>20240326</creationdate><title>Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer</title><author>Park, Soon Sang ; Lee, Young-Kyoung ; Choi, Yong Won ; Lim, Su Bin ; Park, So Hyun ; Kim, Han Ki ; Shin, Jun Sang ; Kim, Young Hwa ; Lee, Dong Hyun ; Kim, Jang-Hee ; Park, Tae Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-896e8ac2c6c357b5cdb2523b28a7147c90920ab117b3637e57db1080608f6df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>cancer buddings</topic><topic>cancer evolution</topic><topic>Cellular Senescence - genetics</topic><topic>collective invasion</topic><topic>colorectal cancer</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - pathology</topic><topic>CP: Cancer</topic><topic>Cyclin-Dependent Kinase Inhibitor p16 - metabolism</topic><topic>Humans</topic><topic>LAMC2</topic><topic>lymph node metastasis</topic><topic>Matrix Metalloproteinase 7 - genetics</topic><topic>MMP7</topic><topic>Phenotype</topic><topic>senescent tumor cells</topic><topic>spatial evolution</topic><topic>spatial transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Soon Sang</creatorcontrib><creatorcontrib>Lee, Young-Kyoung</creatorcontrib><creatorcontrib>Choi, Yong Won</creatorcontrib><creatorcontrib>Lim, Su Bin</creatorcontrib><creatorcontrib>Park, So Hyun</creatorcontrib><creatorcontrib>Kim, Han Ki</creatorcontrib><creatorcontrib>Shin, Jun Sang</creatorcontrib><creatorcontrib>Kim, Young Hwa</creatorcontrib><creatorcontrib>Lee, Dong Hyun</creatorcontrib><creatorcontrib>Kim, Jang-Hee</creatorcontrib><creatorcontrib>Park, Tae Jun</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>DOAJ Directory of Open Access Journals</collection><jtitle>Cell reports (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Soon Sang</au><au>Lee, Young-Kyoung</au><au>Choi, Yong Won</au><au>Lim, Su Bin</au><au>Park, So Hyun</au><au>Kim, Han Ki</au><au>Shin, Jun Sang</au><au>Kim, Young Hwa</au><au>Lee, Dong Hyun</au><au>Kim, Jang-Hee</au><au>Park, Tae Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer</atitle><jtitle>Cell reports (Cambridge)</jtitle><addtitle>Cell Rep</addtitle><date>2024-03-26</date><risdate>2024</risdate><volume>43</volume><issue>3</issue><spage>113912</spage><epage>113912</epage><pages>113912-113912</pages><artnum>113912</artnum><issn>2211-1247</issn><eissn>2211-1247</eissn><abstract>In this study, we explore the dynamic process of colorectal cancer progression, emphasizing the evolution toward a more metastatic phenotype. The term “evolution” as used in this study specifically denotes the phenotypic transition toward a higher metastatic potency from well-formed glandular structures to collective invasion, ultimately resulting in the development of cancer cell buddings at the invasive front. Our findings highlight the spatial correlation of this evolution with tumor cell senescence, revealing distinct types of senescent tumor cells (types I and II) that play different roles in the overall cancer progression. Type I senescent tumor cells (p16INK4A+/CXCL12+/LAMC2−/MMP7−) are identified in the collective invasion region, whereas type II senescent tumor cells (p16INK4A+/CXCL12+/LAMC2+/MMP7+), representing the final evolved form, are prominently located in the partial-EMT region. Importantly, type II senescent tumor cells associate with local invasion and lymph node metastasis in colorectal cancer, potentially affecting patient prognosis.
[Display omitted]
•Cellular senescence is associated with gradual phenotypic transition of cancer cells•Evolutionary path of cancer cells includes two types (I and II) of senescent tumor cells•Type II senescent tumor cells express MMP7 and are associated with higher metastatic potency
Park et al. unravel the spatial heterogeneity of colorectal cancer and gradual phenotypic transition from the center to the invasive front. They demonstrated that cellular senescence is associated with this evolutional transition. Type II senescent tumor cells (p16INK4A+/LAMC2+/MMP7+) were found in the invasive front and are associated with higher metastatic potency.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38446659</pmid><doi>10.1016/j.celrep.2024.113912</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | cancer buddings cancer evolution Cellular Senescence - genetics collective invasion colorectal cancer Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology CP: Cancer Cyclin-Dependent Kinase Inhibitor p16 - metabolism Humans LAMC2 lymph node metastasis Matrix Metalloproteinase 7 - genetics MMP7 Phenotype senescent tumor cells spatial evolution spatial transcriptomics |
title | Cellular senescence is associated with the spatial evolution toward a higher metastatic phenotype in colorectal cancer |
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