Utilizing systems genetics to enhance understanding into molecular targets of skin cancer
Despite progress made with immune checkpoint inhibitors and targeted therapies, skin cancer remains a significant public health concern in the United States. The intricacies of the disease, encompassing genetics, immune responses, and external factors, call for a comprehensive approach. Techniques i...
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Veröffentlicht in: | Experimental dermatology 2024-03, Vol.33 (3), p.e15043-n/a |
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creator | Kim, Minjae J. Kulkarni, Vishnutheertha Goode, Micah A. Hernandez, Jacob Graham, Sean Sivesind, Torunn E. Manchadi, Mary‐Louise |
description | Despite progress made with immune checkpoint inhibitors and targeted therapies, skin cancer remains a significant public health concern in the United States. The intricacies of the disease, encompassing genetics, immune responses, and external factors, call for a comprehensive approach. Techniques in systems genetics, including transcriptional correlation analysis, functional pathway enrichment analysis, and protein–protein interaction network analysis, prove valuable in deciphering intricate molecular mechanisms and identifying potential diagnostic and therapeutic targets for skin cancer. Recent studies demonstrate the efficacy of these techniques in uncovering molecular processes and pinpointing diagnostic markers for various skin cancer types, highlighting the potential of systems genetics in advancing innovative therapies. While certain limitations exist, such as generalizability and contextualization of external factors, the ongoing progress in AI technologies provides hope in overcoming these challenges. By providing protocols and a practical example involving Braf, we aim to inspire early‐career experimental dermatologists to adopt these tools and seamlessly integrate these techniques into their skin cancer research, positioning them at the forefront of innovative approaches in combating this devastating disease. |
doi_str_mv | 10.1111/exd.15043 |
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By providing protocols and a practical example involving Braf, we aim to inspire early‐career experimental dermatologists to adopt these tools and seamlessly integrate these techniques into their skin cancer research, positioning them at the forefront of innovative approaches in combating this devastating disease.</description><subject>Cancer research</subject><subject>Correlation analysis</subject><subject>functional pathway enrichment</subject><subject>Humans</subject><subject>Immune checkpoint inhibitors</subject><subject>Immune response</subject><subject>in silico</subject><subject>Molecular modelling</subject><subject>protein–protein interaction network</subject><subject>Public health</subject><subject>Skin</subject><subject>Skin cancer</subject><subject>Skin Neoplasms - genetics</subject><subject>systems genetics</subject><subject>Therapeutic targets</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1PwyAYB3BiNDpfDn4BQ-JFD92glNIezXxNlnhxiZ6aFh4m2tIJbXR-eqmbHkzkAAd-_PPwR-iYkjENawIfakw5SdgWGtGUkIikMd9GI5KTNEoF4Xto3_sXQqhggu-iPZYlPE_jfISe5p2pzaexC-xXvoPG4wVY6Iz0uGsx2OfSSsC9VeB8V1o1SGPDVdPWIPu6dLgr3QI6j1uN_auxWA5P3CHa0WXt4WhzHqD59dXD9Daa3d_cTS9mkWRJxqJYJZkMMzOiq1hTIXTF4iyvFAchWUbIsOVMxDJOlK50xSktOWNac0VU-PMBOlvnLl371oPvisZ4CXVdWmh7X8Q5T4QIIQM9_UNf2t7ZMF1QWZpTShIe1PlaSdd670AXS2ea0q0KSoqh7yL0XXz3HezJJrGvGlC_8qfgACZr8G5qWP2fVFw9Xq4jvwAisomJ</recordid><startdate>202403</startdate><enddate>202403</enddate><creator>Kim, Minjae J.</creator><creator>Kulkarni, Vishnutheertha</creator><creator>Goode, Micah A.</creator><creator>Hernandez, Jacob</creator><creator>Graham, Sean</creator><creator>Sivesind, Torunn E.</creator><creator>Manchadi, Mary‐Louise</creator><general>Wiley Subscription Services, Inc</general><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>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3445-0619</orcidid></search><sort><creationdate>202403</creationdate><title>Utilizing systems genetics to enhance understanding into molecular targets of skin cancer</title><author>Kim, Minjae J. ; Kulkarni, Vishnutheertha ; Goode, Micah A. ; Hernandez, Jacob ; Graham, Sean ; Sivesind, Torunn E. ; Manchadi, Mary‐Louise</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3483-2d48c60030fb2f177fb3289bd5e7c3800c3809372c24dfbfb511a533ff5d0d043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cancer research</topic><topic>Correlation analysis</topic><topic>functional pathway enrichment</topic><topic>Humans</topic><topic>Immune checkpoint inhibitors</topic><topic>Immune response</topic><topic>in silico</topic><topic>Molecular modelling</topic><topic>protein–protein interaction network</topic><topic>Public health</topic><topic>Skin</topic><topic>Skin cancer</topic><topic>Skin Neoplasms - genetics</topic><topic>systems genetics</topic><topic>Therapeutic targets</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Minjae J.</creatorcontrib><creatorcontrib>Kulkarni, Vishnutheertha</creatorcontrib><creatorcontrib>Goode, Micah A.</creatorcontrib><creatorcontrib>Hernandez, Jacob</creatorcontrib><creatorcontrib>Graham, Sean</creatorcontrib><creatorcontrib>Sivesind, Torunn E.</creatorcontrib><creatorcontrib>Manchadi, Mary‐Louise</creatorcontrib><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>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Minjae J.</au><au>Kulkarni, Vishnutheertha</au><au>Goode, Micah A.</au><au>Hernandez, Jacob</au><au>Graham, Sean</au><au>Sivesind, Torunn E.</au><au>Manchadi, Mary‐Louise</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Utilizing systems genetics to enhance understanding into molecular targets of skin cancer</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2024-03</date><risdate>2024</risdate><volume>33</volume><issue>3</issue><spage>e15043</spage><epage>n/a</epage><pages>e15043-n/a</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>Despite progress made with immune checkpoint inhibitors and targeted therapies, skin cancer remains a significant public health concern in the United States. 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subjects | Cancer research Correlation analysis functional pathway enrichment Humans Immune checkpoint inhibitors Immune response in silico Molecular modelling protein–protein interaction network Public health Skin Skin cancer Skin Neoplasms - genetics systems genetics Therapeutic targets |
title | Utilizing systems genetics to enhance understanding into molecular targets of skin cancer |
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