Progression and perspectives in disease modeling for Juvenile myelomonocytic leukemia
Juvenile myelomonocytic leukemia (JMML) is a rare myeloproliferative neoplasm occurring in infants and young children. JMML has been shown to be resistant to all conventional cytotoxic chemotherapy drugs, and current curative therapies still rely on hematopoietic stem cell transplantation, which car...
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Veröffentlicht in: | Medical oncology (Northwood, London, England) London, England), 2024-12, Vol.42 (1), p.25 |
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container_title | Medical oncology (Northwood, London, England) |
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creator | Fu, Shengyuan Guo, Yao Peng, Zhiyong Zhang, Dengyang Chang, Zhiguang Xiao, Yan Zhang, Qi Yu, Liuting Chen, Chun Chen, Yun Zhao, Yuming |
description | Juvenile myelomonocytic leukemia (JMML) is a rare myeloproliferative neoplasm occurring in infants and young children. JMML has been shown to be resistant to all conventional cytotoxic chemotherapy drugs, and current curative therapies still rely on hematopoietic stem cell transplantation, which carries a high risk of relapse post-transplantation. This underscores the urgent need for novel treatment strategies. However, the rarity of JMML poses a major limitation for research, as it is difficult to collect substantial primary research material. To gain a deeper insight into the underlying biological mechanisms of JMML, researchers are continuously improving and developing preclinical research models to better emulate the disease. Therefore, this review aims to delineate the various experimental models currently employed in JMML, including patient-derived cell-based models, cell models, and animal models. We will discuss the characterization of these models in the context of JMML, hoping to provide a valuable reference for researchers in this field. |
doi_str_mv | 10.1007/s12032-024-02549-5 |
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JMML has been shown to be resistant to all conventional cytotoxic chemotherapy drugs, and current curative therapies still rely on hematopoietic stem cell transplantation, which carries a high risk of relapse post-transplantation. This underscores the urgent need for novel treatment strategies. However, the rarity of JMML poses a major limitation for research, as it is difficult to collect substantial primary research material. To gain a deeper insight into the underlying biological mechanisms of JMML, researchers are continuously improving and developing preclinical research models to better emulate the disease. Therefore, this review aims to delineate the various experimental models currently employed in JMML, including patient-derived cell-based models, cell models, and animal models. We will discuss the characterization of these models in the context of JMML, hoping to provide a valuable reference for researchers in this field.</description><identifier>ISSN: 1357-0560</identifier><identifier>EISSN: 1559-131X</identifier><identifier>DOI: 10.1007/s12032-024-02549-5</identifier><identifier>PMID: 39652257</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Animals ; Disease Models, Animal ; Disease Progression ; Hematology ; Humans ; Internal Medicine ; Leukemia, Myelomonocytic, Juvenile - pathology ; Leukemia, Myelomonocytic, Juvenile - therapy ; Medicine ; Medicine & Public Health ; Oncology ; Pathology ; Review</subject><ispartof>Medical oncology (Northwood, London, England), 2024-12, Vol.42 (1), p.25</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>Copyright Springer Nature B.V. Jan 2025</rights><rights>The Author(s) 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12032-024-02549-5$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12032-024-02549-5$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39652257$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Shengyuan</creatorcontrib><creatorcontrib>Guo, Yao</creatorcontrib><creatorcontrib>Peng, Zhiyong</creatorcontrib><creatorcontrib>Zhang, Dengyang</creatorcontrib><creatorcontrib>Chang, Zhiguang</creatorcontrib><creatorcontrib>Xiao, Yan</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Yu, Liuting</creatorcontrib><creatorcontrib>Chen, Chun</creatorcontrib><creatorcontrib>Chen, Yun</creatorcontrib><creatorcontrib>Zhao, Yuming</creatorcontrib><title>Progression and perspectives in disease modeling for Juvenile myelomonocytic leukemia</title><title>Medical oncology (Northwood, London, England)</title><addtitle>Med Oncol</addtitle><addtitle>Med Oncol</addtitle><description>Juvenile myelomonocytic leukemia (JMML) is a rare myeloproliferative neoplasm occurring in infants and young children. JMML has been shown to be resistant to all conventional cytotoxic chemotherapy drugs, and current curative therapies still rely on hematopoietic stem cell transplantation, which carries a high risk of relapse post-transplantation. This underscores the urgent need for novel treatment strategies. However, the rarity of JMML poses a major limitation for research, as it is difficult to collect substantial primary research material. To gain a deeper insight into the underlying biological mechanisms of JMML, researchers are continuously improving and developing preclinical research models to better emulate the disease. Therefore, this review aims to delineate the various experimental models currently employed in JMML, including patient-derived cell-based models, cell models, and animal models. We will discuss the characterization of these models in the context of JMML, hoping to provide a valuable reference for researchers in this field.</description><subject>Animals</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Hematology</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Leukemia, Myelomonocytic, Juvenile - pathology</subject><subject>Leukemia, Myelomonocytic, Juvenile - therapy</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Review</subject><issn>1357-0560</issn><issn>1559-131X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNpVUU1rGzEQFSWldtz-gRzKQs7bSJodrXUKxSRpgqE5xJCb2I-xI2dX2kpeg_991Dpp2sMww7zHe8M8xs4E_yY4Ly-ikBxkzmWRCgud4wc2FYg6FyAeT9IMWOYcFZ-w0xi3nEuBUn9iE9AKpcRyylb3wW8CxWi9yyrXZgOFOFCzs3uKmXVZayNVkbLet9RZt8nWPmR3456c7dL2QJ3vvfPNYWebrKPxmXpbfWYf11UX6ctrn7HV9dXD4ke-_Hlzu_i-zAeBAnONNYGqUcm6aWssZNFo1FChQk214o2CGgCKQpWi0Ov5upxLqDVIyUveCoIZuzzqDmPdU9uQ24WqM0OwfRUOxlfW_I84-2Q2fm-EUHKO5TwpnL8qBP9rpLgzWz8Gl442IAoJOnmJxPr6r89fg7c_JgIcCTFBbkPhXUZw8zstc0zLpLTMn7QMwguCYIYs</recordid><startdate>20241209</startdate><enddate>20241209</enddate><creator>Fu, Shengyuan</creator><creator>Guo, Yao</creator><creator>Peng, Zhiyong</creator><creator>Zhang, Dengyang</creator><creator>Chang, Zhiguang</creator><creator>Xiao, Yan</creator><creator>Zhang, Qi</creator><creator>Yu, Liuting</creator><creator>Chen, Chun</creator><creator>Chen, Yun</creator><creator>Zhao, Yuming</creator><general>Springer US</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>K9.</scope><scope>5PM</scope></search><sort><creationdate>20241209</creationdate><title>Progression and perspectives in disease modeling for Juvenile myelomonocytic leukemia</title><author>Fu, Shengyuan ; Guo, Yao ; Peng, Zhiyong ; Zhang, Dengyang ; Chang, Zhiguang ; Xiao, Yan ; Zhang, Qi ; Yu, Liuting ; Chen, Chun ; Chen, Yun ; Zhao, Yuming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1515-95be36b562bcdb5424c9593a5659eb60c63b3334467149f8f7823b9322070d1e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Hematology</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Leukemia, Myelomonocytic, Juvenile - pathology</topic><topic>Leukemia, Myelomonocytic, Juvenile - therapy</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Pathology</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Shengyuan</creatorcontrib><creatorcontrib>Guo, Yao</creatorcontrib><creatorcontrib>Peng, Zhiyong</creatorcontrib><creatorcontrib>Zhang, Dengyang</creatorcontrib><creatorcontrib>Chang, Zhiguang</creatorcontrib><creatorcontrib>Xiao, Yan</creatorcontrib><creatorcontrib>Zhang, Qi</creatorcontrib><creatorcontrib>Yu, Liuting</creatorcontrib><creatorcontrib>Chen, Chun</creatorcontrib><creatorcontrib>Chen, Yun</creatorcontrib><creatorcontrib>Zhao, Yuming</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medical oncology (Northwood, London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Shengyuan</au><au>Guo, Yao</au><au>Peng, Zhiyong</au><au>Zhang, Dengyang</au><au>Chang, Zhiguang</au><au>Xiao, Yan</au><au>Zhang, Qi</au><au>Yu, Liuting</au><au>Chen, Chun</au><au>Chen, Yun</au><au>Zhao, Yuming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progression and perspectives in disease modeling for Juvenile myelomonocytic leukemia</atitle><jtitle>Medical oncology (Northwood, London, England)</jtitle><stitle>Med Oncol</stitle><addtitle>Med Oncol</addtitle><date>2024-12-09</date><risdate>2024</risdate><volume>42</volume><issue>1</issue><spage>25</spage><pages>25-</pages><issn>1357-0560</issn><eissn>1559-131X</eissn><abstract>Juvenile myelomonocytic leukemia (JMML) is a rare myeloproliferative neoplasm occurring in infants and young children. JMML has been shown to be resistant to all conventional cytotoxic chemotherapy drugs, and current curative therapies still rely on hematopoietic stem cell transplantation, which carries a high risk of relapse post-transplantation. This underscores the urgent need for novel treatment strategies. However, the rarity of JMML poses a major limitation for research, as it is difficult to collect substantial primary research material. To gain a deeper insight into the underlying biological mechanisms of JMML, researchers are continuously improving and developing preclinical research models to better emulate the disease. Therefore, this review aims to delineate the various experimental models currently employed in JMML, including patient-derived cell-based models, cell models, and animal models. We will discuss the characterization of these models in the context of JMML, hoping to provide a valuable reference for researchers in this field.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>39652257</pmid><doi>10.1007/s12032-024-02549-5</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Disease Models, Animal Disease Progression Hematology Humans Internal Medicine Leukemia, Myelomonocytic, Juvenile - pathology Leukemia, Myelomonocytic, Juvenile - therapy Medicine Medicine & Public Health Oncology Pathology Review |
title | Progression and perspectives in disease modeling for Juvenile myelomonocytic leukemia |
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