Decreased Expression of ZNF554 in Gliomas is Associated with the Activation of Tumor Pathways and Shorter Patient Survival
Zinc finger protein 554 (ZNF554), a member of the Krüppel-associated box domain zinc finger protein subfamily, is predominantly expressed in the brain and placenta in humans. Recently, we unveiled that ZNF554 regulates trophoblast invasion during placentation and its decreased expression leads to th...
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creator | Balogh, Andrea Reiniger, Lilla Hetey, Szabolcs Kiraly, Peter Toth, Eszter Karaszi, Katalin Juhasz, Kata Gelencser, Zsolt Zvara, Agnes Szilagyi, Andras Puskas, Laszlo G Matko, Janos Papp, Zoltan Kovalszky, Ilona Juhasz, Csaba Than, Nandor Gabor |
description | Zinc finger protein 554 (ZNF554), a member of the Krüppel-associated box domain zinc finger protein subfamily, is predominantly expressed in the brain and placenta in humans. Recently, we unveiled that ZNF554 regulates trophoblast invasion during placentation and its decreased expression leads to the early pathogenesis of preeclampsia. Since ZNF proteins are immensely implicated in the development of several tumors including malignant tumors of the brain, here we explored the pathological role of ZNF554 in gliomas.
e examined the expression of ZNF554 at mRNA and protein levels in normal brain and gliomas, and then we searched for genome-wide transcriptomic changes in U87 glioblastoma cells transiently overexpressing
. Immunohistochemistry of brain tissues in our cohort (
= 62) and analysis of large TCGA RNA-Seq data (
= 687) of control, oligodendroglioma, and astrocytoma tissues both revealed decreased expression of
towards higher glioma grades. Furthermore, low
expression was associated with shorter survival of grade III and IV astrocytoma patients. Overexpression of
in U87 cells resulted in differential expression, mostly downregulation of 899 genes. The "PI3K-Akt signaling pathway", known to be activated during glioma development, was the most impacted among 116 dysregulated pathways. Most affected pathways were cancer-related and/or immune-related. Congruently, cell proliferation was decreased and cell cycle was arrested in
-transfected glioma cells. These data collectively suggest that ZNF554 is a potential tumor suppressor and its decreased expression may lead to the loss of oncogene suppression, activation of tumor pathways, and shorter survival of patients with malignant glioma. |
doi_str_mv | 10.3390/ijms21165762 |
format | Article |
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e examined the expression of ZNF554 at mRNA and protein levels in normal brain and gliomas, and then we searched for genome-wide transcriptomic changes in U87 glioblastoma cells transiently overexpressing
. Immunohistochemistry of brain tissues in our cohort (
= 62) and analysis of large TCGA RNA-Seq data (
= 687) of control, oligodendroglioma, and astrocytoma tissues both revealed decreased expression of
towards higher glioma grades. Furthermore, low
expression was associated with shorter survival of grade III and IV astrocytoma patients. Overexpression of
in U87 cells resulted in differential expression, mostly downregulation of 899 genes. The "PI3K-Akt signaling pathway", known to be activated during glioma development, was the most impacted among 116 dysregulated pathways. Most affected pathways were cancer-related and/or immune-related. Congruently, cell proliferation was decreased and cell cycle was arrested in
-transfected glioma cells. These data collectively suggest that ZNF554 is a potential tumor suppressor and its decreased expression may lead to the loss of oncogene suppression, activation of tumor pathways, and shorter survival of patients with malignant glioma.</description><identifier>ISSN: 1422-0067</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21165762</identifier><identifier>PMID: 32796700</identifier><language>eng</language><publisher>Switzerland: MDPI</publisher><subject>Adolescent ; Adult ; Aged ; Brain Neoplasms - genetics ; Brain Neoplasms - pathology ; Cell Cycle Checkpoints - genetics ; Cell Line, Tumor ; Cell Proliferation - genetics ; Female ; Gene Expression Regulation, Neoplastic ; Genome, Human ; Glioma - genetics ; Glioma - pathology ; Humans ; Kruppel-Like Transcription Factors - genetics ; Kruppel-Like Transcription Factors - metabolism ; Male ; Middle Aged ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Signal Transduction ; Survival Analysis ; Young Adult</subject><ispartof>International journal of molecular sciences, 2020-08, Vol.21 (16), p.5762</ispartof><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-f42de3c10df0f64024ada225e841623ed41d43928ddd28f4188cfa50c628dcb3</citedby><cites>FETCH-LOGICAL-c384t-f42de3c10df0f64024ada225e841623ed41d43928ddd28f4188cfa50c628dcb3</cites><orcidid>0000-0002-1773-6861 ; 0000-0002-9188-1987 ; 0000-0001-7149-1482</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461028/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461028/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32796700$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Balogh, Andrea</creatorcontrib><creatorcontrib>Reiniger, Lilla</creatorcontrib><creatorcontrib>Hetey, Szabolcs</creatorcontrib><creatorcontrib>Kiraly, Peter</creatorcontrib><creatorcontrib>Toth, Eszter</creatorcontrib><creatorcontrib>Karaszi, Katalin</creatorcontrib><creatorcontrib>Juhasz, Kata</creatorcontrib><creatorcontrib>Gelencser, Zsolt</creatorcontrib><creatorcontrib>Zvara, Agnes</creatorcontrib><creatorcontrib>Szilagyi, Andras</creatorcontrib><creatorcontrib>Puskas, Laszlo G</creatorcontrib><creatorcontrib>Matko, Janos</creatorcontrib><creatorcontrib>Papp, Zoltan</creatorcontrib><creatorcontrib>Kovalszky, Ilona</creatorcontrib><creatorcontrib>Juhasz, Csaba</creatorcontrib><creatorcontrib>Than, Nandor Gabor</creatorcontrib><title>Decreased Expression of ZNF554 in Gliomas is Associated with the Activation of Tumor Pathways and Shorter Patient Survival</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Zinc finger protein 554 (ZNF554), a member of the Krüppel-associated box domain zinc finger protein subfamily, is predominantly expressed in the brain and placenta in humans. Recently, we unveiled that ZNF554 regulates trophoblast invasion during placentation and its decreased expression leads to the early pathogenesis of preeclampsia. Since ZNF proteins are immensely implicated in the development of several tumors including malignant tumors of the brain, here we explored the pathological role of ZNF554 in gliomas.
e examined the expression of ZNF554 at mRNA and protein levels in normal brain and gliomas, and then we searched for genome-wide transcriptomic changes in U87 glioblastoma cells transiently overexpressing
. Immunohistochemistry of brain tissues in our cohort (
= 62) and analysis of large TCGA RNA-Seq data (
= 687) of control, oligodendroglioma, and astrocytoma tissues both revealed decreased expression of
towards higher glioma grades. Furthermore, low
expression was associated with shorter survival of grade III and IV astrocytoma patients. Overexpression of
in U87 cells resulted in differential expression, mostly downregulation of 899 genes. The "PI3K-Akt signaling pathway", known to be activated during glioma development, was the most impacted among 116 dysregulated pathways. Most affected pathways were cancer-related and/or immune-related. Congruently, cell proliferation was decreased and cell cycle was arrested in
-transfected glioma cells. These data collectively suggest that ZNF554 is a potential tumor suppressor and its decreased expression may lead to the loss of oncogene suppression, activation of tumor pathways, and shorter survival of patients with malignant glioma.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Brain Neoplasms - genetics</subject><subject>Brain Neoplasms - pathology</subject><subject>Cell Cycle Checkpoints - genetics</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - genetics</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genome, Human</subject><subject>Glioma - genetics</subject><subject>Glioma - pathology</subject><subject>Humans</subject><subject>Kruppel-Like Transcription Factors - genetics</subject><subject>Kruppel-Like Transcription Factors - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction</subject><subject>Survival Analysis</subject><subject>Young Adult</subject><issn>1422-0067</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctLxDAQxoMovm-eJUcPrubVtL0Iy_oEUcE9eQkxSW2kbdZMuj7-equusp5mmPnNNx98CO1RcsR5SY79cwuMUpnlkq2gTSoYGxEi89WlfgNtATwTwjjLynW0wVleypyQTfRx6kx0GpzFZ2-z6AB86HCo8MPNeZYJ7Dt80fjQasAe8BggGK_TQL_6VONUOzw2yc91WpxN-zZEfKdT_arfAevO4vs6xOS-h951Cd_3cT5cNDtordINuN1F3UbT87Pp5HJ0fXtxNRlfjwwvRBpVglnHDSW2IpUUhAltNWOZKwSVjDsrqBW8ZIW1lhWVoEVhKp0RI4eReeTb6ORHdtY_ts6awULUjZpF3-r4roL26v-m87V6CnOVC0kJKwaBg4VADC-9g6RaD8Y1je5c6EExwYXIpSi_0MMf1MQAEF3194YS9ZWWWk5rwPeXrf3Bv_HwT_xhkr8</recordid><startdate>20200811</startdate><enddate>20200811</enddate><creator>Balogh, Andrea</creator><creator>Reiniger, Lilla</creator><creator>Hetey, Szabolcs</creator><creator>Kiraly, Peter</creator><creator>Toth, Eszter</creator><creator>Karaszi, Katalin</creator><creator>Juhasz, Kata</creator><creator>Gelencser, Zsolt</creator><creator>Zvara, Agnes</creator><creator>Szilagyi, Andras</creator><creator>Puskas, Laszlo G</creator><creator>Matko, Janos</creator><creator>Papp, Zoltan</creator><creator>Kovalszky, Ilona</creator><creator>Juhasz, Csaba</creator><creator>Than, Nandor Gabor</creator><general>MDPI</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1773-6861</orcidid><orcidid>https://orcid.org/0000-0002-9188-1987</orcidid><orcidid>https://orcid.org/0000-0001-7149-1482</orcidid></search><sort><creationdate>20200811</creationdate><title>Decreased Expression of ZNF554 in Gliomas is Associated with the Activation of Tumor Pathways and Shorter Patient Survival</title><author>Balogh, Andrea ; Reiniger, Lilla ; Hetey, Szabolcs ; Kiraly, Peter ; Toth, Eszter ; Karaszi, Katalin ; Juhasz, Kata ; Gelencser, Zsolt ; Zvara, Agnes ; Szilagyi, Andras ; Puskas, Laszlo G ; Matko, Janos ; Papp, Zoltan ; Kovalszky, Ilona ; Juhasz, Csaba ; Than, Nandor Gabor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-f42de3c10df0f64024ada225e841623ed41d43928ddd28f4188cfa50c628dcb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Brain Neoplasms - genetics</topic><topic>Brain Neoplasms - pathology</topic><topic>Cell Cycle Checkpoints - genetics</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - genetics</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genome, Human</topic><topic>Glioma - genetics</topic><topic>Glioma - pathology</topic><topic>Humans</topic><topic>Kruppel-Like Transcription Factors - genetics</topic><topic>Kruppel-Like Transcription Factors - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction</topic><topic>Survival Analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balogh, Andrea</creatorcontrib><creatorcontrib>Reiniger, Lilla</creatorcontrib><creatorcontrib>Hetey, Szabolcs</creatorcontrib><creatorcontrib>Kiraly, Peter</creatorcontrib><creatorcontrib>Toth, Eszter</creatorcontrib><creatorcontrib>Karaszi, Katalin</creatorcontrib><creatorcontrib>Juhasz, Kata</creatorcontrib><creatorcontrib>Gelencser, Zsolt</creatorcontrib><creatorcontrib>Zvara, Agnes</creatorcontrib><creatorcontrib>Szilagyi, Andras</creatorcontrib><creatorcontrib>Puskas, Laszlo G</creatorcontrib><creatorcontrib>Matko, Janos</creatorcontrib><creatorcontrib>Papp, Zoltan</creatorcontrib><creatorcontrib>Kovalszky, Ilona</creatorcontrib><creatorcontrib>Juhasz, Csaba</creatorcontrib><creatorcontrib>Than, Nandor Gabor</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>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balogh, Andrea</au><au>Reiniger, Lilla</au><au>Hetey, Szabolcs</au><au>Kiraly, Peter</au><au>Toth, Eszter</au><au>Karaszi, Katalin</au><au>Juhasz, Kata</au><au>Gelencser, Zsolt</au><au>Zvara, Agnes</au><au>Szilagyi, Andras</au><au>Puskas, Laszlo G</au><au>Matko, Janos</au><au>Papp, Zoltan</au><au>Kovalszky, Ilona</au><au>Juhasz, Csaba</au><au>Than, Nandor Gabor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased Expression of ZNF554 in Gliomas is Associated with the Activation of Tumor Pathways and Shorter Patient Survival</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2020-08-11</date><risdate>2020</risdate><volume>21</volume><issue>16</issue><spage>5762</spage><pages>5762-</pages><issn>1422-0067</issn><eissn>1422-0067</eissn><abstract>Zinc finger protein 554 (ZNF554), a member of the Krüppel-associated box domain zinc finger protein subfamily, is predominantly expressed in the brain and placenta in humans. Recently, we unveiled that ZNF554 regulates trophoblast invasion during placentation and its decreased expression leads to the early pathogenesis of preeclampsia. Since ZNF proteins are immensely implicated in the development of several tumors including malignant tumors of the brain, here we explored the pathological role of ZNF554 in gliomas.
e examined the expression of ZNF554 at mRNA and protein levels in normal brain and gliomas, and then we searched for genome-wide transcriptomic changes in U87 glioblastoma cells transiently overexpressing
. Immunohistochemistry of brain tissues in our cohort (
= 62) and analysis of large TCGA RNA-Seq data (
= 687) of control, oligodendroglioma, and astrocytoma tissues both revealed decreased expression of
towards higher glioma grades. Furthermore, low
expression was associated with shorter survival of grade III and IV astrocytoma patients. Overexpression of
in U87 cells resulted in differential expression, mostly downregulation of 899 genes. The "PI3K-Akt signaling pathway", known to be activated during glioma development, was the most impacted among 116 dysregulated pathways. Most affected pathways were cancer-related and/or immune-related. Congruently, cell proliferation was decreased and cell cycle was arrested in
-transfected glioma cells. These data collectively suggest that ZNF554 is a potential tumor suppressor and its decreased expression may lead to the loss of oncogene suppression, activation of tumor pathways, and shorter survival of patients with malignant glioma.</abstract><cop>Switzerland</cop><pub>MDPI</pub><pmid>32796700</pmid><doi>10.3390/ijms21165762</doi><orcidid>https://orcid.org/0000-0002-1773-6861</orcidid><orcidid>https://orcid.org/0000-0002-9188-1987</orcidid><orcidid>https://orcid.org/0000-0001-7149-1482</orcidid><oa>free_for_read</oa></addata></record> |
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source | MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adolescent Adult Aged Brain Neoplasms - genetics Brain Neoplasms - pathology Cell Cycle Checkpoints - genetics Cell Line, Tumor Cell Proliferation - genetics Female Gene Expression Regulation, Neoplastic Genome, Human Glioma - genetics Glioma - pathology Humans Kruppel-Like Transcription Factors - genetics Kruppel-Like Transcription Factors - metabolism Male Middle Aged RNA, Messenger - genetics RNA, Messenger - metabolism Signal Transduction Survival Analysis Young Adult |
title | Decreased Expression of ZNF554 in Gliomas is Associated with the Activation of Tumor Pathways and Shorter Patient Survival |
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