Frequent increased gene copy number and high protein expression of tRNA (cytosine-5-)-methyltransferase (NSUN2) in human cancers
NSUN2, also known as SAKI or MISU, is a methyltransferase which catalyses (cytosine-5-)-methylation of tRNA. The human NSUN2 gene is located on chromosome 5p15.31-33. We show that NSUN2 gene copy number is increased in oral and colorectal cancers. Protein expression levels of NSUN2 were determined b...
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Veröffentlicht in: | DNA and cell biology 2012-05, Vol.31 (5), p.660-671 |
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creator | Okamoto, Mayumi Hirata, Sumi Sato, Sunao Koga, Satomi Fujii, Mikiko Qi, Guangying Ogawa, Ikuko Takata, Takashi Shimamoto, Fumio Tatsuka, Masaaki |
description | NSUN2, also known as SAKI or MISU, is a methyltransferase which catalyses (cytosine-5-)-methylation of tRNA. The human NSUN2 gene is located on chromosome 5p15.31-33. We show that NSUN2 gene copy number is increased in oral and colorectal cancers. Protein expression levels of NSUN2 were determined by immunoblot using novel polyclonal antibodies raised against a synthetic peptide corresponding to the C-terminal region of the protein. In most normal tissues, NSUN2 expression levels were extremely low. On the other hand, oral and colorectal cancers typically expressed high levels of NSUN2. The level of NSUN2 was similar in interphase and mitotic cells, and immunohistochemical analysis demonstrated strong staining for NSUN2 in oral and colon cancer tissues when compared with normal tissues, providing a distinct diagnostic significance for NSUN2 in comparison with Ki-67, a widely used marker of actively proliferating cells. In addition, elevated protein expression of NSUN2 was confirmed by immunohistochemical analysis of various cancers including esophageal, stomach, liver, pancreas, uterine cervix, prostate, kidney, bladder, thyroid, and breast cancers. NSUN2 is regulated by Aurora-B, a newly developed molecular target for cancer therapy, leading us to propose that NSUN2 might become a valuable target for cancer therapy and a cancer diagnostic marker. |
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The human NSUN2 gene is located on chromosome 5p15.31-33. We show that NSUN2 gene copy number is increased in oral and colorectal cancers. Protein expression levels of NSUN2 were determined by immunoblot using novel polyclonal antibodies raised against a synthetic peptide corresponding to the C-terminal region of the protein. In most normal tissues, NSUN2 expression levels were extremely low. On the other hand, oral and colorectal cancers typically expressed high levels of NSUN2. The level of NSUN2 was similar in interphase and mitotic cells, and immunohistochemical analysis demonstrated strong staining for NSUN2 in oral and colon cancer tissues when compared with normal tissues, providing a distinct diagnostic significance for NSUN2 in comparison with Ki-67, a widely used marker of actively proliferating cells. In addition, elevated protein expression of NSUN2 was confirmed by immunohistochemical analysis of various cancers including esophageal, stomach, liver, pancreas, uterine cervix, prostate, kidney, bladder, thyroid, and breast cancers. NSUN2 is regulated by Aurora-B, a newly developed molecular target for cancer therapy, leading us to propose that NSUN2 might become a valuable target for cancer therapy and a cancer diagnostic marker.</description><identifier>ISSN: 1044-5498</identifier><identifier>EISSN: 1557-7430</identifier><identifier>DOI: 10.1089/dna.2011.1446</identifier><identifier>PMID: 22136356</identifier><language>eng</language><publisher>United States</publisher><subject>Antibodies ; Blotting, Southern ; Breast cancer ; Catalysis ; Cells, Cultured ; Cervix ; chromosome 5 ; Colon cancer ; Colorectal cancer ; copy number ; Esophagus ; Fibroblasts ; Gastric cancer ; Gene Dosage ; Humans ; Immunoblotting ; Immunoenzyme Techniques ; In Situ Hybridization, Fluorescence ; Interphase ; Keratinocytes - cytology ; Keratinocytes - metabolism ; Kidney ; Liver ; Methyltransferase ; Methyltransferases - genetics ; Methyltransferases - metabolism ; Neoplasms - genetics ; Neoplasms - metabolism ; Neoplasms - pathology ; Pancreas ; Prostate ; Stomach ; synthetic peptides ; Thyroid ; tRNA ; Urinary bladder ; Uterus</subject><ispartof>DNA and cell biology, 2012-05, Vol.31 (5), p.660-671</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-8d5eeb652f08ac574d832c62628d465cd191a59ed9162cdf611e30483d0278773</citedby><cites>FETCH-LOGICAL-c392t-8d5eeb652f08ac574d832c62628d465cd191a59ed9162cdf611e30483d0278773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22136356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okamoto, Mayumi</creatorcontrib><creatorcontrib>Hirata, Sumi</creatorcontrib><creatorcontrib>Sato, Sunao</creatorcontrib><creatorcontrib>Koga, Satomi</creatorcontrib><creatorcontrib>Fujii, Mikiko</creatorcontrib><creatorcontrib>Qi, Guangying</creatorcontrib><creatorcontrib>Ogawa, Ikuko</creatorcontrib><creatorcontrib>Takata, Takashi</creatorcontrib><creatorcontrib>Shimamoto, Fumio</creatorcontrib><creatorcontrib>Tatsuka, Masaaki</creatorcontrib><title>Frequent increased gene copy number and high protein expression of tRNA (cytosine-5-)-methyltransferase (NSUN2) in human cancers</title><title>DNA and cell biology</title><addtitle>DNA Cell Biol</addtitle><description>NSUN2, also known as SAKI or MISU, is a methyltransferase which catalyses (cytosine-5-)-methylation of tRNA. The human NSUN2 gene is located on chromosome 5p15.31-33. We show that NSUN2 gene copy number is increased in oral and colorectal cancers. Protein expression levels of NSUN2 were determined by immunoblot using novel polyclonal antibodies raised against a synthetic peptide corresponding to the C-terminal region of the protein. In most normal tissues, NSUN2 expression levels were extremely low. On the other hand, oral and colorectal cancers typically expressed high levels of NSUN2. The level of NSUN2 was similar in interphase and mitotic cells, and immunohistochemical analysis demonstrated strong staining for NSUN2 in oral and colon cancer tissues when compared with normal tissues, providing a distinct diagnostic significance for NSUN2 in comparison with Ki-67, a widely used marker of actively proliferating cells. In addition, elevated protein expression of NSUN2 was confirmed by immunohistochemical analysis of various cancers including esophageal, stomach, liver, pancreas, uterine cervix, prostate, kidney, bladder, thyroid, and breast cancers. NSUN2 is regulated by Aurora-B, a newly developed molecular target for cancer therapy, leading us to propose that NSUN2 might become a valuable target for cancer therapy and a cancer diagnostic marker.</description><subject>Antibodies</subject><subject>Blotting, Southern</subject><subject>Breast cancer</subject><subject>Catalysis</subject><subject>Cells, Cultured</subject><subject>Cervix</subject><subject>chromosome 5</subject><subject>Colon cancer</subject><subject>Colorectal cancer</subject><subject>copy number</subject><subject>Esophagus</subject><subject>Fibroblasts</subject><subject>Gastric cancer</subject><subject>Gene Dosage</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Immunoenzyme Techniques</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Interphase</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - metabolism</subject><subject>Kidney</subject><subject>Liver</subject><subject>Methyltransferase</subject><subject>Methyltransferases - genetics</subject><subject>Methyltransferases - metabolism</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Pancreas</subject><subject>Prostate</subject><subject>Stomach</subject><subject>synthetic peptides</subject><subject>Thyroid</subject><subject>tRNA</subject><subject>Urinary bladder</subject><subject>Uterus</subject><issn>1044-5498</issn><issn>1557-7430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkTtPwzAUhS0EorxGVuSxDC5-xxkrxEuqisRjjlz7pg1qnGInEt346bjiMTPdO3w6R0cfQueMThg15ZUPdsIpYxMmpd5DR0ypghRS0P38UymJkqUZoeOU3iilijN6iEacM6GF0kfo8zbC-wChx01wEWwCj5cQALtus8VhaBcQsQ0er5rlCm9i10MTMHxsIqTUdAF3Ne6f5lM8dtu-S00AosglaaFfbdd9tCHVEHMqHs-fX-f8Mtfg1dDagJ0NDmI6RQe1XSc4-7kn6PX25uX6nswe7x6upzPiRMl7YrwCWGjFa2qsU4X0RnCnuebGS62cZyWzqgRfMs2drzVjIKg0wlNemKIQJ2j8nZs35MGpr9omOVivbYBuSBWj3FBJy1L9A2VK6oJxkVHyjbrYpRShrjaxaW3cZqja-amyn2rnp9r5yfzFT_SwaMH_0b9CxBdOcoqP</recordid><startdate>201205</startdate><enddate>201205</enddate><creator>Okamoto, Mayumi</creator><creator>Hirata, Sumi</creator><creator>Sato, Sunao</creator><creator>Koga, Satomi</creator><creator>Fujii, Mikiko</creator><creator>Qi, Guangying</creator><creator>Ogawa, Ikuko</creator><creator>Takata, Takashi</creator><creator>Shimamoto, Fumio</creator><creator>Tatsuka, Masaaki</creator><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201205</creationdate><title>Frequent increased gene copy number and high protein expression of tRNA (cytosine-5-)-methyltransferase (NSUN2) in human cancers</title><author>Okamoto, Mayumi ; Hirata, Sumi ; Sato, Sunao ; Koga, Satomi ; Fujii, Mikiko ; Qi, Guangying ; Ogawa, Ikuko ; Takata, Takashi ; Shimamoto, Fumio ; Tatsuka, Masaaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-8d5eeb652f08ac574d832c62628d465cd191a59ed9162cdf611e30483d0278773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Antibodies</topic><topic>Blotting, Southern</topic><topic>Breast cancer</topic><topic>Catalysis</topic><topic>Cells, Cultured</topic><topic>Cervix</topic><topic>chromosome 5</topic><topic>Colon cancer</topic><topic>Colorectal cancer</topic><topic>copy number</topic><topic>Esophagus</topic><topic>Fibroblasts</topic><topic>Gastric cancer</topic><topic>Gene Dosage</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Immunoenzyme Techniques</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Interphase</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - metabolism</topic><topic>Kidney</topic><topic>Liver</topic><topic>Methyltransferase</topic><topic>Methyltransferases - genetics</topic><topic>Methyltransferases - metabolism</topic><topic>Neoplasms - genetics</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Pancreas</topic><topic>Prostate</topic><topic>Stomach</topic><topic>synthetic peptides</topic><topic>Thyroid</topic><topic>tRNA</topic><topic>Urinary bladder</topic><topic>Uterus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okamoto, Mayumi</creatorcontrib><creatorcontrib>Hirata, Sumi</creatorcontrib><creatorcontrib>Sato, Sunao</creatorcontrib><creatorcontrib>Koga, Satomi</creatorcontrib><creatorcontrib>Fujii, Mikiko</creatorcontrib><creatorcontrib>Qi, Guangying</creatorcontrib><creatorcontrib>Ogawa, Ikuko</creatorcontrib><creatorcontrib>Takata, Takashi</creatorcontrib><creatorcontrib>Shimamoto, Fumio</creatorcontrib><creatorcontrib>Tatsuka, Masaaki</creatorcontrib><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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>DNA and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okamoto, Mayumi</au><au>Hirata, Sumi</au><au>Sato, Sunao</au><au>Koga, Satomi</au><au>Fujii, Mikiko</au><au>Qi, Guangying</au><au>Ogawa, Ikuko</au><au>Takata, Takashi</au><au>Shimamoto, Fumio</au><au>Tatsuka, Masaaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frequent increased gene copy number and high protein expression of tRNA (cytosine-5-)-methyltransferase (NSUN2) in human cancers</atitle><jtitle>DNA and cell biology</jtitle><addtitle>DNA Cell Biol</addtitle><date>2012-05</date><risdate>2012</risdate><volume>31</volume><issue>5</issue><spage>660</spage><epage>671</epage><pages>660-671</pages><issn>1044-5498</issn><eissn>1557-7430</eissn><abstract>NSUN2, also known as SAKI or MISU, is a methyltransferase which catalyses (cytosine-5-)-methylation of tRNA. The human NSUN2 gene is located on chromosome 5p15.31-33. We show that NSUN2 gene copy number is increased in oral and colorectal cancers. Protein expression levels of NSUN2 were determined by immunoblot using novel polyclonal antibodies raised against a synthetic peptide corresponding to the C-terminal region of the protein. In most normal tissues, NSUN2 expression levels were extremely low. On the other hand, oral and colorectal cancers typically expressed high levels of NSUN2. The level of NSUN2 was similar in interphase and mitotic cells, and immunohistochemical analysis demonstrated strong staining for NSUN2 in oral and colon cancer tissues when compared with normal tissues, providing a distinct diagnostic significance for NSUN2 in comparison with Ki-67, a widely used marker of actively proliferating cells. In addition, elevated protein expression of NSUN2 was confirmed by immunohistochemical analysis of various cancers including esophageal, stomach, liver, pancreas, uterine cervix, prostate, kidney, bladder, thyroid, and breast cancers. NSUN2 is regulated by Aurora-B, a newly developed molecular target for cancer therapy, leading us to propose that NSUN2 might become a valuable target for cancer therapy and a cancer diagnostic marker.</abstract><cop>United States</cop><pmid>22136356</pmid><doi>10.1089/dna.2011.1446</doi><tpages>12</tpages></addata></record> |
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subjects | Antibodies Blotting, Southern Breast cancer Catalysis Cells, Cultured Cervix chromosome 5 Colon cancer Colorectal cancer copy number Esophagus Fibroblasts Gastric cancer Gene Dosage Humans Immunoblotting Immunoenzyme Techniques In Situ Hybridization, Fluorescence Interphase Keratinocytes - cytology Keratinocytes - metabolism Kidney Liver Methyltransferase Methyltransferases - genetics Methyltransferases - metabolism Neoplasms - genetics Neoplasms - metabolism Neoplasms - pathology Pancreas Prostate Stomach synthetic peptides Thyroid tRNA Urinary bladder Uterus |
title | Frequent increased gene copy number and high protein expression of tRNA (cytosine-5-)-methyltransferase (NSUN2) in human cancers |
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