Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy
Tumor suppressor p53 plays a central role in tumor suppression. p53 is the most frequently mutated gene in human cancer, and over half of human cancers contain p53 mutations. Majority of p53 mutations in cancer are missense mutations, leading to the expression of full-length mutant p53 (mutp53) prot...
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Veröffentlicht in: | Journal of molecular biology 2017-06, Vol.429 (11), p.1595-1606 |
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description | Tumor suppressor p53 plays a central role in tumor suppression. p53 is the most frequently mutated gene in human cancer, and over half of human cancers contain p53 mutations. Majority of p53 mutations in cancer are missense mutations, leading to the expression of full-length mutant p53 (mutp53) protein. While the critical role of wild-type p53 in tumor suppression has been firmly established, mounting evidence has demonstrated that many tumor-associated mutp53 proteins not only lose the tumor-suppressive function of wild-type p53 but also gain new activities to promote tumorigenesis independently of wild-type p53, termed gain-of-function. Mutant p53 protein often accumulates to very high levels in tumors, contributing to malignant progression. Recently, mutp53 has become an attractive target for cancer therapy. Further understanding of the mechanisms underlying mutp53 protein accumulation and gain-of-function will accelerate the development of targeted therapies for human cancer harboring mutp53. In this review, we summarize the recent advances in the studies on mutp53 protein accumulation and gain-of-function and targeted therapies for mutp53 in human cancer.
[Display omitted]
•p53 is the most commonly mutated gene in human cancer.•Mutant p53 is frequently accumulated to high levels in cancer.•Mutant p53 often displays gain-of-function oncogenic activities.•Targeting mutp53 is a promising therapeutic strategy for cancer. |
doi_str_mv | 10.1016/j.jmb.2017.03.030 |
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•p53 is the most commonly mutated gene in human cancer.•Mutant p53 is frequently accumulated to high levels in cancer.•Mutant p53 often displays gain-of-function oncogenic activities.•Targeting mutp53 is a promising therapeutic strategy for cancer.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/j.jmb.2017.03.030</identifier><identifier>PMID: 28390900</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Carcinogenesis ; Disease Models, Animal ; gain-of-function ; gain-of-function mutation ; genes ; Humans ; missense mutation ; mutant p53 ; Mutant Proteins - antagonists & inhibitors ; Mutant Proteins - genetics ; Mutant Proteins - metabolism ; mutants ; Mutation, Missense ; neoplasms ; Neoplasms - pathology ; Neoplasms - therapy ; p53 ; protein stabilization ; proteins ; targeted therapy ; therapeutics ; Tumor Suppressor Protein p53 - antagonists & inhibitors ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>Journal of molecular biology, 2017-06, Vol.429 (11), p.1595-1606</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-b205c497242c619220fa854395e673f3f7e167e9de2f272284a18eaf73c3e33a3</citedby><cites>FETCH-LOGICAL-c550t-b205c497242c619220fa854395e673f3f7e167e9de2f272284a18eaf73c3e33a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022283617301638$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28390900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yue, Xuetian</creatorcontrib><creatorcontrib>Zhao, Yuhan</creatorcontrib><creatorcontrib>Xu, Yang</creatorcontrib><creatorcontrib>Zheng, Min</creatorcontrib><creatorcontrib>Feng, Zhaohui</creatorcontrib><creatorcontrib>Hu, Wenwei</creatorcontrib><title>Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>Tumor suppressor p53 plays a central role in tumor suppression. p53 is the most frequently mutated gene in human cancer, and over half of human cancers contain p53 mutations. Majority of p53 mutations in cancer are missense mutations, leading to the expression of full-length mutant p53 (mutp53) protein. While the critical role of wild-type p53 in tumor suppression has been firmly established, mounting evidence has demonstrated that many tumor-associated mutp53 proteins not only lose the tumor-suppressive function of wild-type p53 but also gain new activities to promote tumorigenesis independently of wild-type p53, termed gain-of-function. Mutant p53 protein often accumulates to very high levels in tumors, contributing to malignant progression. Recently, mutp53 has become an attractive target for cancer therapy. Further understanding of the mechanisms underlying mutp53 protein accumulation and gain-of-function will accelerate the development of targeted therapies for human cancer harboring mutp53. In this review, we summarize the recent advances in the studies on mutp53 protein accumulation and gain-of-function and targeted therapies for mutp53 in human cancer.
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•p53 is the most commonly mutated gene in human cancer.•Mutant p53 is frequently accumulated to high levels in cancer.•Mutant p53 often displays gain-of-function oncogenic activities.•Targeting mutp53 is a promising therapeutic strategy for cancer.</description><subject>Animals</subject><subject>Carcinogenesis</subject><subject>Disease Models, Animal</subject><subject>gain-of-function</subject><subject>gain-of-function mutation</subject><subject>genes</subject><subject>Humans</subject><subject>missense mutation</subject><subject>mutant p53</subject><subject>Mutant Proteins - antagonists & inhibitors</subject><subject>Mutant Proteins - genetics</subject><subject>Mutant Proteins - metabolism</subject><subject>mutants</subject><subject>Mutation, Missense</subject><subject>neoplasms</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - therapy</subject><subject>p53</subject><subject>protein stabilization</subject><subject>proteins</subject><subject>targeted therapy</subject><subject>therapeutics</subject><subject>Tumor Suppressor Protein p53 - antagonists & inhibitors</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kNFLwzAQxoMobk7_AF-kjz7YeUnaplUQxnBTmPiizyFLr5rRpjNpB_vvzZiKvggfHNx9993xI-ScwpgCza5X41WzHDOgYgw8CA7IkEJexHnG80MyBGAsZjnPBuTE-xUApDzJj8kg9AooAIZk8tR3ynbROuWRsdFUWY3uJppo3Td9rTrT2qtoroyN2yqe9VbvO8qW0cs7OrXenpKjStUez77qiLzO7l-mD_Hief44nSxinabQxUsGqU4KwRKmM1owBpXK04QXKWaCV7wSSDOBRYmsYoKxPFE0R1UJrjlyrviI3O1z1_2ywVKj7Zyq5dqZRrmtbJWRfyfWvMu3diPTLONMJCHg8ivAtR89-k42xmusa2Wx7b1kgU8iKDAIVrq3atd677D6OUNB7tDLlQzo5Q69BB6027n4_d_PxjfrYLjdGzBQ2hh00muDgXdpHOpOlq35J_4TaUiSkg</recordid><startdate>20170602</startdate><enddate>20170602</enddate><creator>Yue, Xuetian</creator><creator>Zhao, Yuhan</creator><creator>Xu, Yang</creator><creator>Zheng, Min</creator><creator>Feng, Zhaohui</creator><creator>Hu, Wenwei</creator><general>Elsevier Ltd</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>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20170602</creationdate><title>Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy</title><author>Yue, Xuetian ; Zhao, Yuhan ; Xu, Yang ; Zheng, Min ; Feng, Zhaohui ; Hu, Wenwei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c550t-b205c497242c619220fa854395e673f3f7e167e9de2f272284a18eaf73c3e33a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Carcinogenesis</topic><topic>Disease Models, Animal</topic><topic>gain-of-function</topic><topic>gain-of-function mutation</topic><topic>genes</topic><topic>Humans</topic><topic>missense mutation</topic><topic>mutant p53</topic><topic>Mutant Proteins - antagonists & inhibitors</topic><topic>Mutant Proteins - genetics</topic><topic>Mutant Proteins - metabolism</topic><topic>mutants</topic><topic>Mutation, Missense</topic><topic>neoplasms</topic><topic>Neoplasms - pathology</topic><topic>Neoplasms - therapy</topic><topic>p53</topic><topic>protein stabilization</topic><topic>proteins</topic><topic>targeted therapy</topic><topic>therapeutics</topic><topic>Tumor Suppressor Protein p53 - antagonists & inhibitors</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yue, Xuetian</creatorcontrib><creatorcontrib>Zhao, Yuhan</creatorcontrib><creatorcontrib>Xu, Yang</creatorcontrib><creatorcontrib>Zheng, Min</creatorcontrib><creatorcontrib>Feng, Zhaohui</creatorcontrib><creatorcontrib>Hu, Wenwei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yue, Xuetian</au><au>Zhao, Yuhan</au><au>Xu, Yang</au><au>Zheng, Min</au><au>Feng, Zhaohui</au><au>Hu, Wenwei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2017-06-02</date><risdate>2017</risdate><volume>429</volume><issue>11</issue><spage>1595</spage><epage>1606</epage><pages>1595-1606</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><abstract>Tumor suppressor p53 plays a central role in tumor suppression. p53 is the most frequently mutated gene in human cancer, and over half of human cancers contain p53 mutations. Majority of p53 mutations in cancer are missense mutations, leading to the expression of full-length mutant p53 (mutp53) protein. While the critical role of wild-type p53 in tumor suppression has been firmly established, mounting evidence has demonstrated that many tumor-associated mutp53 proteins not only lose the tumor-suppressive function of wild-type p53 but also gain new activities to promote tumorigenesis independently of wild-type p53, termed gain-of-function. Mutant p53 protein often accumulates to very high levels in tumors, contributing to malignant progression. Recently, mutp53 has become an attractive target for cancer therapy. Further understanding of the mechanisms underlying mutp53 protein accumulation and gain-of-function will accelerate the development of targeted therapies for human cancer harboring mutp53. In this review, we summarize the recent advances in the studies on mutp53 protein accumulation and gain-of-function and targeted therapies for mutp53 in human cancer.
[Display omitted]
•p53 is the most commonly mutated gene in human cancer.•Mutant p53 is frequently accumulated to high levels in cancer.•Mutant p53 often displays gain-of-function oncogenic activities.•Targeting mutp53 is a promising therapeutic strategy for cancer.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28390900</pmid><doi>10.1016/j.jmb.2017.03.030</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Carcinogenesis Disease Models, Animal gain-of-function gain-of-function mutation genes Humans missense mutation mutant p53 Mutant Proteins - antagonists & inhibitors Mutant Proteins - genetics Mutant Proteins - metabolism mutants Mutation, Missense neoplasms Neoplasms - pathology Neoplasms - therapy p53 protein stabilization proteins targeted therapy therapeutics Tumor Suppressor Protein p53 - antagonists & inhibitors Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism |
title | Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy |
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