Expression of p53 and human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen with inhibition of apoptosis in HHV‐8–associated malignancies
BACKGROUND Kaposi sarcoma (KS) and primary effusion lymphoma (PEL) cells express human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen (LANA) (open reading frame [ORF] 73 protein), suggesting that LANA plays an important role in the pathogenesis of HHV‐8–associated malignancies. Rec...
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description | BACKGROUND
Kaposi sarcoma (KS) and primary effusion lymphoma (PEL) cells express human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen (LANA) (open reading frame [ORF] 73 protein), suggesting that LANA plays an important role in the pathogenesis of HHV‐8–associated malignancies. Recently, the binding of LANA to p53 was demonstrated in vitro. In the current study, the authors investigated the association between p53 and LANA expression with apoptosis in HHV‐8–associated malignancies in vivo.
METHODS
Twenty‐six cases of KS, 1 case of HHV‐8–associated solid lymphoma, 2 PEL cell lines, and an HHV‐8–associated lymphoma engrafted in severe combined immunodeficiency (SCID) mice were examined. Immunohistochemistry using the catalyzed signal amplification system was employed to detect LANA and p53 on paraffin embedded tissues and the immunofluorescence technique was used on cell lines. To detect apoptosis, the TdT‐mediated dUTP nick end labeling (TUNEL) method was used. For mutation analysis of p53, exons 5–9 of the p53 gene were amplified by polymerase chain reaction and examined by direct sequencing.
RESULTS
Immunohistochemistry revealed that LANA and p53 were expressed in the tumor cells of all these specimens, and apoptotic cells were rarely detected in them using the TUNEL method. Immunofluorescence assay revealed that LANA colocalized with p53 in the nuclei of PEL cells. Sequencing analysis indicated that there was no mutation in the deduced amino acid sequences of p53 in KS tissues.
CONCLUSIONS
These data suggest colocalization of p53 and LANA and the inhibition of apoptosis in HHV‐8–associated malignancies in vivo, supporting the results found in vitro that p53 inhibition by LANA suppresses cell death, as reported previously. These results also suggest that the p53 pathway is crucial in the pathogenesis of HHV‐8–associated malignancies. Cancer 2001;92:3076–84. © 2001 American Cancer Society.
In Kaposi sarcoma and primary effusion lymphoma, herpesvirus‐8–encoded latency‐associated nuclear antigen (LANA) and p53 were expressed, but very rarely was apoptosis identified. In addition, no mutation was detected in the sequences of p53, suggesting that LANA inhibits p53‐dependent apoptosis. |
doi_str_mv | 10.1002/1097-0142(20011215)92:12<3076::AID-CNCR10117>3.0.CO;2-D |
format | Article |
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Kaposi sarcoma (KS) and primary effusion lymphoma (PEL) cells express human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen (LANA) (open reading frame [ORF] 73 protein), suggesting that LANA plays an important role in the pathogenesis of HHV‐8–associated malignancies. Recently, the binding of LANA to p53 was demonstrated in vitro. In the current study, the authors investigated the association between p53 and LANA expression with apoptosis in HHV‐8–associated malignancies in vivo.
METHODS
Twenty‐six cases of KS, 1 case of HHV‐8–associated solid lymphoma, 2 PEL cell lines, and an HHV‐8–associated lymphoma engrafted in severe combined immunodeficiency (SCID) mice were examined. Immunohistochemistry using the catalyzed signal amplification system was employed to detect LANA and p53 on paraffin embedded tissues and the immunofluorescence technique was used on cell lines. To detect apoptosis, the TdT‐mediated dUTP nick end labeling (TUNEL) method was used. For mutation analysis of p53, exons 5–9 of the p53 gene were amplified by polymerase chain reaction and examined by direct sequencing.
RESULTS
Immunohistochemistry revealed that LANA and p53 were expressed in the tumor cells of all these specimens, and apoptotic cells were rarely detected in them using the TUNEL method. Immunofluorescence assay revealed that LANA colocalized with p53 in the nuclei of PEL cells. Sequencing analysis indicated that there was no mutation in the deduced amino acid sequences of p53 in KS tissues.
CONCLUSIONS
These data suggest colocalization of p53 and LANA and the inhibition of apoptosis in HHV‐8–associated malignancies in vivo, supporting the results found in vitro that p53 inhibition by LANA suppresses cell death, as reported previously. These results also suggest that the p53 pathway is crucial in the pathogenesis of HHV‐8–associated malignancies. Cancer 2001;92:3076–84. © 2001 American Cancer Society.
In Kaposi sarcoma and primary effusion lymphoma, herpesvirus‐8–encoded latency‐associated nuclear antigen (LANA) and p53 were expressed, but very rarely was apoptosis identified. In addition, no mutation was detected in the sequences of p53, suggesting that LANA inhibits p53‐dependent apoptosis.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(20011215)92:12<3076::AID-CNCR10117>3.0.CO;2-D</identifier><identifier>PMID: 11753987</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Acquired Immunodeficiency Syndrome - complications ; Adult ; Aged ; Aged, 80 and over ; Animals ; Antigens, Viral ; Apoptosis ; Biological and medical sciences ; Cell Transformation, Neoplastic ; Female ; Gene Expression Regulation, Neoplastic ; Hematologic and hematopoietic diseases ; Herpesviridae Infections - genetics ; Herpesvirus 8, Human - genetics ; human herpesvirus 8 ; human herpesvirus‐8 (HHV‐8) ; Humans ; Immunohistochemistry ; Kaposi sarcoma (KS) ; LANA protein ; latency-associated nuclear antigen ; latency‐associated nuclear antigen (LANA) ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Lymphoma - genetics ; Male ; Malformations of the eye ; Medical sciences ; Mice ; Mice, SCID ; Middle Aged ; Nuclear Proteins - genetics ; Ophthalmology ; p53 ; Polymerase Chain Reaction ; Sarcoma, Kaposi - genetics ; TdT‐mediated dUTP nick end labeling (TUNEL) ; Tumor Suppressor Protein p53 - biosynthesis</subject><ispartof>Cancer, 2001-12, Vol.92 (12), p.3076-3084</ispartof><rights>Copyright © 2001 American Cancer Society</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2001 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5147-37c644696b6662de7d154f73f12bc5764805770689706a0acf8cdd7db3a167bb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F1097-0142%2820011215%2992%3A12%3C3076%3A%3AAID-CNCR10117%3E3.0.CO%3B2-D$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F1097-0142%2820011215%2992%3A12%3C3076%3A%3AAID-CNCR10117%3E3.0.CO%3B2-D$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27903,27904,45553,45554,46387,46811</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13383516$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11753987$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katano, Harutaka</creatorcontrib><creatorcontrib>Sato, Yuko</creatorcontrib><creatorcontrib>Sata, Tetsutaro</creatorcontrib><title>Expression of p53 and human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen with inhibition of apoptosis in HHV‐8–associated malignancies</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND
Kaposi sarcoma (KS) and primary effusion lymphoma (PEL) cells express human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen (LANA) (open reading frame [ORF] 73 protein), suggesting that LANA plays an important role in the pathogenesis of HHV‐8–associated malignancies. Recently, the binding of LANA to p53 was demonstrated in vitro. In the current study, the authors investigated the association between p53 and LANA expression with apoptosis in HHV‐8–associated malignancies in vivo.
METHODS
Twenty‐six cases of KS, 1 case of HHV‐8–associated solid lymphoma, 2 PEL cell lines, and an HHV‐8–associated lymphoma engrafted in severe combined immunodeficiency (SCID) mice were examined. Immunohistochemistry using the catalyzed signal amplification system was employed to detect LANA and p53 on paraffin embedded tissues and the immunofluorescence technique was used on cell lines. To detect apoptosis, the TdT‐mediated dUTP nick end labeling (TUNEL) method was used. For mutation analysis of p53, exons 5–9 of the p53 gene were amplified by polymerase chain reaction and examined by direct sequencing.
RESULTS
Immunohistochemistry revealed that LANA and p53 were expressed in the tumor cells of all these specimens, and apoptotic cells were rarely detected in them using the TUNEL method. Immunofluorescence assay revealed that LANA colocalized with p53 in the nuclei of PEL cells. Sequencing analysis indicated that there was no mutation in the deduced amino acid sequences of p53 in KS tissues.
CONCLUSIONS
These data suggest colocalization of p53 and LANA and the inhibition of apoptosis in HHV‐8–associated malignancies in vivo, supporting the results found in vitro that p53 inhibition by LANA suppresses cell death, as reported previously. These results also suggest that the p53 pathway is crucial in the pathogenesis of HHV‐8–associated malignancies. Cancer 2001;92:3076–84. © 2001 American Cancer Society.
In Kaposi sarcoma and primary effusion lymphoma, herpesvirus‐8–encoded latency‐associated nuclear antigen (LANA) and p53 were expressed, but very rarely was apoptosis identified. In addition, no mutation was detected in the sequences of p53, suggesting that LANA inhibits p53‐dependent apoptosis.</description><subject>Acquired Immunodeficiency Syndrome - complications</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Animals</subject><subject>Antigens, Viral</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Cell Transformation, Neoplastic</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Herpesviridae Infections - genetics</subject><subject>Herpesvirus 8, Human - genetics</subject><subject>human herpesvirus 8</subject><subject>human herpesvirus‐8 (HHV‐8)</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kaposi sarcoma (KS)</subject><subject>LANA protein</subject><subject>latency-associated nuclear antigen</subject><subject>latency‐associated nuclear antigen (LANA)</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Lymphoma - genetics</subject><subject>Male</subject><subject>Malformations of the eye</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Middle Aged</subject><subject>Nuclear Proteins - genetics</subject><subject>Ophthalmology</subject><subject>p53</subject><subject>Polymerase Chain Reaction</subject><subject>Sarcoma, Kaposi - genetics</subject><subject>TdT‐mediated dUTP nick end labeling (TUNEL)</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkctu1DAUhi0EokPhFZA3oHaRwZfYTgYEqjKFqVQxEuK2QZZjOx2j3IgTyuz6CEi8Aw_WJ8HRhA4bhNjYPr__8_vIHwAvMJpjhMgTjFIRIRyTI4IQxgSz45QsMHlGkeCLxcnZMspeZ29wuBPP6RzNs_VTEi1vgdlN520wQwglEYvpxwNwz_vPoRSE0bvgIHQxmiZiBn6efms7671ratgUsGUUqtrAzVCpGm5s11r_1XWDv776nsCj1er9eDi-vvpha90Ya2Cp-nDcBll532gXSgPrQZdWdSGqdxe2hpeu30BXb1zu-ukl1TZt33jngw6n3BD7R0ilSndRq1o76--DO4UqvX0w7Yfg3cvTt9kqOl-_OstOziPNcCwiKjSPY57ynHNOjBUGs7gQtMAk10zwOEFMCMSTNCwKKV0k2hhhcqowF3lOD8HjXW7bNV8G63tZOa9tWaraNoOXglDBSIz_acQJSZDASTB-2Bl113jf2UK2natUt5UYyZG1HInJkZj8zVqmQSVyZC1lYC1vWEsqkczWkshlSH44jTDklTX73AluMDyaDMprVRbd-Jd-76M0oQzz4Pu081260m7_c76_jbcX6S9hrNhP</recordid><startdate>20011215</startdate><enddate>20011215</enddate><creator>Katano, Harutaka</creator><creator>Sato, Yuko</creator><creator>Sata, Tetsutaro</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><scope>IQODW</scope><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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20011215</creationdate><title>Expression of p53 and human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen with inhibition of apoptosis in HHV‐8–associated malignancies</title><author>Katano, Harutaka ; Sato, Yuko ; Sata, Tetsutaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5147-37c644696b6662de7d154f73f12bc5764805770689706a0acf8cdd7db3a167bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Acquired Immunodeficiency Syndrome - complications</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Animals</topic><topic>Antigens, Viral</topic><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Cell Transformation, Neoplastic</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Herpesviridae Infections - genetics</topic><topic>Herpesvirus 8, Human - genetics</topic><topic>human herpesvirus 8</topic><topic>human herpesvirus‐8 (HHV‐8)</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kaposi sarcoma (KS)</topic><topic>LANA protein</topic><topic>latency-associated nuclear antigen</topic><topic>latency‐associated nuclear antigen (LANA)</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Lymphoma - genetics</topic><topic>Male</topic><topic>Malformations of the eye</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, SCID</topic><topic>Middle Aged</topic><topic>Nuclear Proteins - genetics</topic><topic>Ophthalmology</topic><topic>p53</topic><topic>Polymerase Chain Reaction</topic><topic>Sarcoma, Kaposi - genetics</topic><topic>TdT‐mediated dUTP nick end labeling (TUNEL)</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katano, Harutaka</creatorcontrib><creatorcontrib>Sato, Yuko</creatorcontrib><creatorcontrib>Sata, Tetsutaro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katano, Harutaka</au><au>Sato, Yuko</au><au>Sata, Tetsutaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of p53 and human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen with inhibition of apoptosis in HHV‐8–associated malignancies</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2001-12-15</date><risdate>2001</risdate><volume>92</volume><issue>12</issue><spage>3076</spage><epage>3084</epage><pages>3076-3084</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND
Kaposi sarcoma (KS) and primary effusion lymphoma (PEL) cells express human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen (LANA) (open reading frame [ORF] 73 protein), suggesting that LANA plays an important role in the pathogenesis of HHV‐8–associated malignancies. Recently, the binding of LANA to p53 was demonstrated in vitro. In the current study, the authors investigated the association between p53 and LANA expression with apoptosis in HHV‐8–associated malignancies in vivo.
METHODS
Twenty‐six cases of KS, 1 case of HHV‐8–associated solid lymphoma, 2 PEL cell lines, and an HHV‐8–associated lymphoma engrafted in severe combined immunodeficiency (SCID) mice were examined. Immunohistochemistry using the catalyzed signal amplification system was employed to detect LANA and p53 on paraffin embedded tissues and the immunofluorescence technique was used on cell lines. To detect apoptosis, the TdT‐mediated dUTP nick end labeling (TUNEL) method was used. For mutation analysis of p53, exons 5–9 of the p53 gene were amplified by polymerase chain reaction and examined by direct sequencing.
RESULTS
Immunohistochemistry revealed that LANA and p53 were expressed in the tumor cells of all these specimens, and apoptotic cells were rarely detected in them using the TUNEL method. Immunofluorescence assay revealed that LANA colocalized with p53 in the nuclei of PEL cells. Sequencing analysis indicated that there was no mutation in the deduced amino acid sequences of p53 in KS tissues.
CONCLUSIONS
These data suggest colocalization of p53 and LANA and the inhibition of apoptosis in HHV‐8–associated malignancies in vivo, supporting the results found in vitro that p53 inhibition by LANA suppresses cell death, as reported previously. These results also suggest that the p53 pathway is crucial in the pathogenesis of HHV‐8–associated malignancies. Cancer 2001;92:3076–84. © 2001 American Cancer Society.
In Kaposi sarcoma and primary effusion lymphoma, herpesvirus‐8–encoded latency‐associated nuclear antigen (LANA) and p53 were expressed, but very rarely was apoptosis identified. In addition, no mutation was detected in the sequences of p53, suggesting that LANA inhibits p53‐dependent apoptosis.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>11753987</pmid><doi>10.1002/1097-0142(20011215)92:12<3076::AID-CNCR10117>3.0.CO;2-D</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acquired Immunodeficiency Syndrome - complications Adult Aged Aged, 80 and over Animals Antigens, Viral Apoptosis Biological and medical sciences Cell Transformation, Neoplastic Female Gene Expression Regulation, Neoplastic Hematologic and hematopoietic diseases Herpesviridae Infections - genetics Herpesvirus 8, Human - genetics human herpesvirus 8 human herpesvirus‐8 (HHV‐8) Humans Immunohistochemistry Kaposi sarcoma (KS) LANA protein latency-associated nuclear antigen latency‐associated nuclear antigen (LANA) Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Lymphoma - genetics Male Malformations of the eye Medical sciences Mice Mice, SCID Middle Aged Nuclear Proteins - genetics Ophthalmology p53 Polymerase Chain Reaction Sarcoma, Kaposi - genetics TdT‐mediated dUTP nick end labeling (TUNEL) Tumor Suppressor Protein p53 - biosynthesis |
title | Expression of p53 and human herpesvirus‐8 (HHV‐8)–encoded latency‐associated nuclear antigen with inhibition of apoptosis in HHV‐8–associated malignancies |
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