Mutation spectrum of the p53 gene in bone and soft tissue sarcomas
We present here an analysis of the spectrum of mutations of the p53 gene seen in 127 bone and soft tissue sarcomas of various histological classifications. Gross rearrangements were analyzed by Southern blotting using a complementary DNA probe from the p53 gene, and subtle alterations in the entire...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1992-11, Vol.52 (22), p.6194-6199 |
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creator | TOGUCHIDA, J YAMAGUCHI, T WEICHSELBAUM, R. R ISHIZAKI, K YANDELL, D. W RITCHIE, B BEAUCHAMP, R. L DAYTON, S. H HERRERA, G. E YAMAMURO, T KOTOURA, Y SASAKI, M. S LITTLE, J. B |
description | We present here an analysis of the spectrum of mutations of the p53 gene seen in 127 bone and soft tissue sarcomas of various histological classifications. Gross rearrangements were analyzed by Southern blotting using a complementary DNA probe from the p53 gene, and subtle alterations in the entire coding sequence (exons 2 through 11) were identified by a combination of single-strand conformation polymorphism analysis and direct genomic sequencing. A total of 42 somatic alterations of the p53 gene were found, of which 21 were gross rearrangements and 21 were subtle alterations. These included 17 cases of a single base substitution, 3 small deletions, and one single base insertion. In contrast to reported findings for other types of cancer, we found that mutations of the p53 gene in sarcomas are quite heterogeneous both in their distribution throughout the gene and in the type of genetic alterations that result. All 13 missense mutations we found occurred at highly conserved residues, whereas 8 nonsense mutations occurred at sites that spanned the gene from codons 46 to 316. Surprisingly, approximately one-half of the osteosarcomas with allelic deletions on 17p did not have detectable alterations in the coding sequence of the p53 gene. |
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R ; ISHIZAKI, K ; YANDELL, D. W ; RITCHIE, B ; BEAUCHAMP, R. L ; DAYTON, S. H ; HERRERA, G. E ; YAMAMURO, T ; KOTOURA, Y ; SASAKI, M. S ; LITTLE, J. B</creator><creatorcontrib>TOGUCHIDA, J ; YAMAGUCHI, T ; WEICHSELBAUM, R. R ; ISHIZAKI, K ; YANDELL, D. W ; RITCHIE, B ; BEAUCHAMP, R. L ; DAYTON, S. H ; HERRERA, G. E ; YAMAMURO, T ; KOTOURA, Y ; SASAKI, M. S ; LITTLE, J. B</creatorcontrib><description>We present here an analysis of the spectrum of mutations of the p53 gene seen in 127 bone and soft tissue sarcomas of various histological classifications. Gross rearrangements were analyzed by Southern blotting using a complementary DNA probe from the p53 gene, and subtle alterations in the entire coding sequence (exons 2 through 11) were identified by a combination of single-strand conformation polymorphism analysis and direct genomic sequencing. A total of 42 somatic alterations of the p53 gene were found, of which 21 were gross rearrangements and 21 were subtle alterations. These included 17 cases of a single base substitution, 3 small deletions, and one single base insertion. In contrast to reported findings for other types of cancer, we found that mutations of the p53 gene in sarcomas are quite heterogeneous both in their distribution throughout the gene and in the type of genetic alterations that result. All 13 missense mutations we found occurred at highly conserved residues, whereas 8 nonsense mutations occurred at sites that spanned the gene from codons 46 to 316. Surprisingly, approximately one-half of the osteosarcomas with allelic deletions on 17p did not have detectable alterations in the coding sequence of the p53 gene.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 1423262</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Alleles ; Base Sequence ; Biological and medical sciences ; Blotting, Southern ; Bone Neoplasms - genetics ; Diseases of the osteoarticular system ; Exons - genetics ; Gene Deletion ; Gene Rearrangement - genetics ; Genes, p53 - genetics ; Humans ; Medical sciences ; Molecular Sequence Data ; Mutation ; Osteosarcoma - genetics ; Phenotype ; Sarcoma - genetics ; Soft Tissue Neoplasms - genetics ; Tumors of striated muscle and skeleton</subject><ispartof>Cancer research (Chicago, Ill.), 1992-11, Vol.52 (22), p.6194-6199</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4412574$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1423262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TOGUCHIDA, J</creatorcontrib><creatorcontrib>YAMAGUCHI, T</creatorcontrib><creatorcontrib>WEICHSELBAUM, R. 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Gross rearrangements were analyzed by Southern blotting using a complementary DNA probe from the p53 gene, and subtle alterations in the entire coding sequence (exons 2 through 11) were identified by a combination of single-strand conformation polymorphism analysis and direct genomic sequencing. A total of 42 somatic alterations of the p53 gene were found, of which 21 were gross rearrangements and 21 were subtle alterations. These included 17 cases of a single base substitution, 3 small deletions, and one single base insertion. In contrast to reported findings for other types of cancer, we found that mutations of the p53 gene in sarcomas are quite heterogeneous both in their distribution throughout the gene and in the type of genetic alterations that result. All 13 missense mutations we found occurred at highly conserved residues, whereas 8 nonsense mutations occurred at sites that spanned the gene from codons 46 to 316. Surprisingly, approximately one-half of the osteosarcomas with allelic deletions on 17p did not have detectable alterations in the coding sequence of the p53 gene.</description><subject>Alleles</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Blotting, Southern</subject><subject>Bone Neoplasms - genetics</subject><subject>Diseases of the osteoarticular system</subject><subject>Exons - genetics</subject><subject>Gene Deletion</subject><subject>Gene Rearrangement - genetics</subject><subject>Genes, p53 - genetics</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Osteosarcoma - genetics</subject><subject>Phenotype</subject><subject>Sarcoma - genetics</subject><subject>Soft Tissue Neoplasms - genetics</subject><subject>Tumors of striated muscle and skeleton</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j0tLxDAUhYMoYx39CUIW4q6Qx00fSx18wYgbXZc0c-NU2qbmpgv_vQWLq8Ph-zhwTlgmja7yEsCcskwIUeUGSnXOLoi-lmqkMBu2kaC0KlTG7l_nZFMXRk4TuhTngQfP0xH5ZDT_xBF5N_I2LGnHA6fgE08d0YycbHRhsHTJzrztCa_W3LKPx4f33XO-f3t62d3t86Mq6pQ7b1UBhRGyNlqU0HrpTQFaoPC6rqU2WBiwlQTUxmlnhRRQtYtaldLLWm_Z7d_uFMP3jJSaoSOHfW9HDDM1pVbLsoJFvF7FuR3w0EyxG2z8adbTC79ZuSVnex_t6Dr61wCkMiXoX-esXdQ</recordid><startdate>19921115</startdate><enddate>19921115</enddate><creator>TOGUCHIDA, J</creator><creator>YAMAGUCHI, T</creator><creator>WEICHSELBAUM, R. 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R</au><au>ISHIZAKI, K</au><au>YANDELL, D. W</au><au>RITCHIE, B</au><au>BEAUCHAMP, R. L</au><au>DAYTON, S. H</au><au>HERRERA, G. E</au><au>YAMAMURO, T</au><au>KOTOURA, Y</au><au>SASAKI, M. S</au><au>LITTLE, J. B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mutation spectrum of the p53 gene in bone and soft tissue sarcomas</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1992-11-15</date><risdate>1992</risdate><volume>52</volume><issue>22</issue><spage>6194</spage><epage>6199</epage><pages>6194-6199</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>We present here an analysis of the spectrum of mutations of the p53 gene seen in 127 bone and soft tissue sarcomas of various histological classifications. Gross rearrangements were analyzed by Southern blotting using a complementary DNA probe from the p53 gene, and subtle alterations in the entire coding sequence (exons 2 through 11) were identified by a combination of single-strand conformation polymorphism analysis and direct genomic sequencing. A total of 42 somatic alterations of the p53 gene were found, of which 21 were gross rearrangements and 21 were subtle alterations. These included 17 cases of a single base substitution, 3 small deletions, and one single base insertion. In contrast to reported findings for other types of cancer, we found that mutations of the p53 gene in sarcomas are quite heterogeneous both in their distribution throughout the gene and in the type of genetic alterations that result. All 13 missense mutations we found occurred at highly conserved residues, whereas 8 nonsense mutations occurred at sites that spanned the gene from codons 46 to 316. Surprisingly, approximately one-half of the osteosarcomas with allelic deletions on 17p did not have detectable alterations in the coding sequence of the p53 gene.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>1423262</pmid><tpages>6</tpages></addata></record> |
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subjects | Alleles Base Sequence Biological and medical sciences Blotting, Southern Bone Neoplasms - genetics Diseases of the osteoarticular system Exons - genetics Gene Deletion Gene Rearrangement - genetics Genes, p53 - genetics Humans Medical sciences Molecular Sequence Data Mutation Osteosarcoma - genetics Phenotype Sarcoma - genetics Soft Tissue Neoplasms - genetics Tumors of striated muscle and skeleton |
title | Mutation spectrum of the p53 gene in bone and soft tissue sarcomas |
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