RNA-Seq Analysis Reveals Dendrobium officinale Polysaccharides Inhibit Precancerous Lesions of Gastric Cancer through PER3 and AQP4
Purpose. There has been mounting evidence that Dendrobium officinale polysaccharides (DOP), a traditional Chinese medicine, are a potential candidate treatment for N-methyl-N′-nitro-N-nitrosoguanidine- (MNNG-) induced precancerous lesions of gastric cancer (PLGC). However, the underlying mechanisms...
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description | Purpose. There has been mounting evidence that Dendrobium officinale polysaccharides (DOP), a traditional Chinese medicine, are a potential candidate treatment for N-methyl-N′-nitro-N-nitrosoguanidine- (MNNG-) induced precancerous lesions of gastric cancer (PLGC). However, the underlying mechanisms have not been adequately addressed. Method. We utilized RNA-Seq analysis to investigate possible molecular targets and then used Venn software to identify the differentially expressed genes (DEGs). Further, we analyzed these DEGs with core analysis, upstream analysis, and interaction network analysis by IPA software and validated the DEGs by real-time PCR and Western blot. Result. 78 DEGs were identified from the normal control group (CON), the PLGC model group (MOD), and the DOP-treated group (DOP) by the Venn software. Further analysis of these DEGs, including core analysis, upstream analysis, and interaction network analysis, was performed by Ingenuity Pathway Analysis (IPA). The main canonical pathways involved were SPINK1 Pancreatic Cancer Pathway (−log (P value) = 4.45, ratio = 0.0667) and Circadian Rhythm Signaling (−log (P value) = 2.33, ratio = 0.0606). Circadian Rhythm Signaling was strongly upregulated in the model group versus the DOP group. CLOCK was predicted to be strongly activated (z-score = 2.236) in upstream analysis and induced the downstream PER3. In addition, the relative mRNA expression levels of seven DEGs (CD2AP, ECM1, AQP4, PER3, CMTM4, ESRRG, and KCNJ15) from RT-PCR agreed with RNA-Seq data from MOD versus CON and MOD versus DOP groups. The gene and protein expression levels of PER3 and AQP4 were significantly downregulated in the PLGC model and significantly increased by DOP treatment (9.6 g/kg). Conclusions. These findings not only showed DOP inhibits PLGC development by upregulating the PER3 and AQP4 gene and protein expression but also suggested that its mechanism of action involved modulating the Circadian Rhythm Signaling pathway. |
doi_str_mv | 10.1155/2021/3036504 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8550840</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2591231019</sourcerecordid><originalsourceid>FETCH-LOGICAL-c448t-a6a2f30cfd10ecfb290c8aea8c38bfa687cbdc4a650018a85d5aedcbb004c3813</originalsourceid><addsrcrecordid>eNp90UFv0zAUB3ALMbExuHFGlrggsTDbcRLnglSVMSZVUApI3KwX52XxlNqbnQztzBefS7sKOHCypffzs5__hLzg7C3nRXEqmOCnOcvLgslH5IhXkmdSKPV4v69-HJKnMV4xJuqqqp6Qw1xWgpeiOiK_Vp9m2Ve8oTMHw120ka7wFmGI9D26NvjGTmvqu84amwDSpU8KjOkh2BYjvXC9bexIlwENOIPBT5EuMFrvYjpHzyGOwRo6_12kY5_AZU-XZ6ucgmvp7MtSPiMHXboRn-_WY_L9w9m3-cds8fn8Yj5bZEZKNWZQguhyZrqWMzRdI2pmFCAok6umg1JVpmmNhPQRjCtQRVsAtqZpGJOJ8PyYvNv2vZ6adaqgGwMM-jrYNYQ77cHqvyvO9vrS32pVFExJlhq83jUI_mbCOOq1jQaHARymubUoai5yznid6Kt_6JWfQvrCjVJ1yVlKIqmTrTLBxxiw2z-GM71JV2_S1bt0E3_55wB7_BBnAm-2oLeuhZ_2_-3uAYL8rng</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2589610777</pqid></control><display><type>article</type><title>RNA-Seq Analysis Reveals Dendrobium officinale Polysaccharides Inhibit Precancerous Lesions of Gastric Cancer through PER3 and AQP4</title><source>Wiley-Blackwell Open Access Titles</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>PubMed Central Open Access</source><creator>Zhao, Yi ; Huang, Hong-xia ; Tang, Su-yuan ; Sun, You-zhi</creator><contributor>Roman Junior, Walter Antonio ; Walter Antonio Roman Junior</contributor><creatorcontrib>Zhao, Yi ; Huang, Hong-xia ; Tang, Su-yuan ; Sun, You-zhi ; Roman Junior, Walter Antonio ; Walter Antonio Roman Junior</creatorcontrib><description>Purpose. There has been mounting evidence that Dendrobium officinale polysaccharides (DOP), a traditional Chinese medicine, are a potential candidate treatment for N-methyl-N′-nitro-N-nitrosoguanidine- (MNNG-) induced precancerous lesions of gastric cancer (PLGC). However, the underlying mechanisms have not been adequately addressed. Method. We utilized RNA-Seq analysis to investigate possible molecular targets and then used Venn software to identify the differentially expressed genes (DEGs). Further, we analyzed these DEGs with core analysis, upstream analysis, and interaction network analysis by IPA software and validated the DEGs by real-time PCR and Western blot. Result. 78 DEGs were identified from the normal control group (CON), the PLGC model group (MOD), and the DOP-treated group (DOP) by the Venn software. Further analysis of these DEGs, including core analysis, upstream analysis, and interaction network analysis, was performed by Ingenuity Pathway Analysis (IPA). The main canonical pathways involved were SPINK1 Pancreatic Cancer Pathway (−log (P value) = 4.45, ratio = 0.0667) and Circadian Rhythm Signaling (−log (P value) = 2.33, ratio = 0.0606). Circadian Rhythm Signaling was strongly upregulated in the model group versus the DOP group. CLOCK was predicted to be strongly activated (z-score = 2.236) in upstream analysis and induced the downstream PER3. In addition, the relative mRNA expression levels of seven DEGs (CD2AP, ECM1, AQP4, PER3, CMTM4, ESRRG, and KCNJ15) from RT-PCR agreed with RNA-Seq data from MOD versus CON and MOD versus DOP groups. The gene and protein expression levels of PER3 and AQP4 were significantly downregulated in the PLGC model and significantly increased by DOP treatment (9.6 g/kg). Conclusions. These findings not only showed DOP inhibits PLGC development by upregulating the PER3 and AQP4 gene and protein expression but also suggested that its mechanism of action involved modulating the Circadian Rhythm Signaling pathway.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2021/3036504</identifier><identifier>PMID: 34721627</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Antibodies ; Aquaporin 4 ; Binding sites ; Chinese medicine ; Circadian rhythms ; Computer programs ; Dendrobium officinale ; Drug dosages ; Evidence-based medicine ; Gastric cancer ; Gene expression ; Laboratory animals ; Nonsteroidal anti-inflammatory drugs ; Pancreatic cancer ; Period 3 protein ; Polymerase chain reaction ; Polysaccharides ; Protein expression ; Proteins ; Signal transduction ; Software ; Traditional Chinese medicine ; Variance analysis</subject><ispartof>Evidence-based complementary and alternative medicine, 2021, Vol.2021, p.3036504-10</ispartof><rights>Copyright © 2021 Yi Zhao et al.</rights><rights>Copyright © 2021 Yi Zhao et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2021 Yi Zhao et al. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-a6a2f30cfd10ecfb290c8aea8c38bfa687cbdc4a650018a85d5aedcbb004c3813</citedby><cites>FETCH-LOGICAL-c448t-a6a2f30cfd10ecfb290c8aea8c38bfa687cbdc4a650018a85d5aedcbb004c3813</cites><orcidid>0000-0001-9692-0562 ; 0000-0002-9633-646X ; 0000-0002-5449-8428 ; 0000-0003-1995-6144</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/PMC8550840/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550840/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,4010,27902,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34721627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Roman Junior, Walter Antonio</contributor><contributor>Walter Antonio Roman Junior</contributor><creatorcontrib>Zhao, Yi</creatorcontrib><creatorcontrib>Huang, Hong-xia</creatorcontrib><creatorcontrib>Tang, Su-yuan</creatorcontrib><creatorcontrib>Sun, You-zhi</creatorcontrib><title>RNA-Seq Analysis Reveals Dendrobium officinale Polysaccharides Inhibit Precancerous Lesions of Gastric Cancer through PER3 and AQP4</title><title>Evidence-based complementary and alternative medicine</title><addtitle>Evid Based Complement Alternat Med</addtitle><description>Purpose. There has been mounting evidence that Dendrobium officinale polysaccharides (DOP), a traditional Chinese medicine, are a potential candidate treatment for N-methyl-N′-nitro-N-nitrosoguanidine- (MNNG-) induced precancerous lesions of gastric cancer (PLGC). However, the underlying mechanisms have not been adequately addressed. Method. We utilized RNA-Seq analysis to investigate possible molecular targets and then used Venn software to identify the differentially expressed genes (DEGs). Further, we analyzed these DEGs with core analysis, upstream analysis, and interaction network analysis by IPA software and validated the DEGs by real-time PCR and Western blot. Result. 78 DEGs were identified from the normal control group (CON), the PLGC model group (MOD), and the DOP-treated group (DOP) by the Venn software. Further analysis of these DEGs, including core analysis, upstream analysis, and interaction network analysis, was performed by Ingenuity Pathway Analysis (IPA). The main canonical pathways involved were SPINK1 Pancreatic Cancer Pathway (−log (P value) = 4.45, ratio = 0.0667) and Circadian Rhythm Signaling (−log (P value) = 2.33, ratio = 0.0606). Circadian Rhythm Signaling was strongly upregulated in the model group versus the DOP group. CLOCK was predicted to be strongly activated (z-score = 2.236) in upstream analysis and induced the downstream PER3. In addition, the relative mRNA expression levels of seven DEGs (CD2AP, ECM1, AQP4, PER3, CMTM4, ESRRG, and KCNJ15) from RT-PCR agreed with RNA-Seq data from MOD versus CON and MOD versus DOP groups. The gene and protein expression levels of PER3 and AQP4 were significantly downregulated in the PLGC model and significantly increased by DOP treatment (9.6 g/kg). Conclusions. These findings not only showed DOP inhibits PLGC development by upregulating the PER3 and AQP4 gene and protein expression but also suggested that its mechanism of action involved modulating the Circadian Rhythm Signaling pathway.</description><subject>Antibodies</subject><subject>Aquaporin 4</subject><subject>Binding sites</subject><subject>Chinese medicine</subject><subject>Circadian rhythms</subject><subject>Computer programs</subject><subject>Dendrobium officinale</subject><subject>Drug dosages</subject><subject>Evidence-based medicine</subject><subject>Gastric cancer</subject><subject>Gene expression</subject><subject>Laboratory animals</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Pancreatic cancer</subject><subject>Period 3 protein</subject><subject>Polymerase chain reaction</subject><subject>Polysaccharides</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Software</subject><subject>Traditional Chinese medicine</subject><subject>Variance analysis</subject><issn>1741-427X</issn><issn>1741-4288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp90UFv0zAUB3ALMbExuHFGlrggsTDbcRLnglSVMSZVUApI3KwX52XxlNqbnQztzBefS7sKOHCypffzs5__hLzg7C3nRXEqmOCnOcvLgslH5IhXkmdSKPV4v69-HJKnMV4xJuqqqp6Qw1xWgpeiOiK_Vp9m2Ve8oTMHw120ka7wFmGI9D26NvjGTmvqu84amwDSpU8KjOkh2BYjvXC9bexIlwENOIPBT5EuMFrvYjpHzyGOwRo6_12kY5_AZU-XZ6ucgmvp7MtSPiMHXboRn-_WY_L9w9m3-cds8fn8Yj5bZEZKNWZQguhyZrqWMzRdI2pmFCAok6umg1JVpmmNhPQRjCtQRVsAtqZpGJOJ8PyYvNv2vZ6adaqgGwMM-jrYNYQ77cHqvyvO9vrS32pVFExJlhq83jUI_mbCOOq1jQaHARymubUoai5yznid6Kt_6JWfQvrCjVJ1yVlKIqmTrTLBxxiw2z-GM71JV2_S1bt0E3_55wB7_BBnAm-2oLeuhZ_2_-3uAYL8rng</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Zhao, Yi</creator><creator>Huang, Hong-xia</creator><creator>Tang, Su-yuan</creator><creator>Sun, You-zhi</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9692-0562</orcidid><orcidid>https://orcid.org/0000-0002-9633-646X</orcidid><orcidid>https://orcid.org/0000-0002-5449-8428</orcidid><orcidid>https://orcid.org/0000-0003-1995-6144</orcidid></search><sort><creationdate>2021</creationdate><title>RNA-Seq Analysis Reveals Dendrobium officinale Polysaccharides Inhibit Precancerous Lesions of Gastric Cancer through PER3 and AQP4</title><author>Zhao, Yi ; Huang, Hong-xia ; Tang, Su-yuan ; Sun, You-zhi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-a6a2f30cfd10ecfb290c8aea8c38bfa687cbdc4a650018a85d5aedcbb004c3813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antibodies</topic><topic>Aquaporin 4</topic><topic>Binding sites</topic><topic>Chinese medicine</topic><topic>Circadian rhythms</topic><topic>Computer programs</topic><topic>Dendrobium officinale</topic><topic>Drug dosages</topic><topic>Evidence-based medicine</topic><topic>Gastric cancer</topic><topic>Gene expression</topic><topic>Laboratory animals</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Pancreatic cancer</topic><topic>Period 3 protein</topic><topic>Polymerase chain reaction</topic><topic>Polysaccharides</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Signal transduction</topic><topic>Software</topic><topic>Traditional Chinese medicine</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Yi</creatorcontrib><creatorcontrib>Huang, Hong-xia</creatorcontrib><creatorcontrib>Tang, Su-yuan</creatorcontrib><creatorcontrib>Sun, You-zhi</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Yi</au><au>Huang, Hong-xia</au><au>Tang, Su-yuan</au><au>Sun, You-zhi</au><au>Roman Junior, Walter Antonio</au><au>Walter Antonio Roman Junior</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RNA-Seq Analysis Reveals Dendrobium officinale Polysaccharides Inhibit Precancerous Lesions of Gastric Cancer through PER3 and AQP4</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2021</date><risdate>2021</risdate><volume>2021</volume><spage>3036504</spage><epage>10</epage><pages>3036504-10</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Purpose. There has been mounting evidence that Dendrobium officinale polysaccharides (DOP), a traditional Chinese medicine, are a potential candidate treatment for N-methyl-N′-nitro-N-nitrosoguanidine- (MNNG-) induced precancerous lesions of gastric cancer (PLGC). However, the underlying mechanisms have not been adequately addressed. Method. We utilized RNA-Seq analysis to investigate possible molecular targets and then used Venn software to identify the differentially expressed genes (DEGs). Further, we analyzed these DEGs with core analysis, upstream analysis, and interaction network analysis by IPA software and validated the DEGs by real-time PCR and Western blot. Result. 78 DEGs were identified from the normal control group (CON), the PLGC model group (MOD), and the DOP-treated group (DOP) by the Venn software. Further analysis of these DEGs, including core analysis, upstream analysis, and interaction network analysis, was performed by Ingenuity Pathway Analysis (IPA). The main canonical pathways involved were SPINK1 Pancreatic Cancer Pathway (−log (P value) = 4.45, ratio = 0.0667) and Circadian Rhythm Signaling (−log (P value) = 2.33, ratio = 0.0606). Circadian Rhythm Signaling was strongly upregulated in the model group versus the DOP group. CLOCK was predicted to be strongly activated (z-score = 2.236) in upstream analysis and induced the downstream PER3. In addition, the relative mRNA expression levels of seven DEGs (CD2AP, ECM1, AQP4, PER3, CMTM4, ESRRG, and KCNJ15) from RT-PCR agreed with RNA-Seq data from MOD versus CON and MOD versus DOP groups. The gene and protein expression levels of PER3 and AQP4 were significantly downregulated in the PLGC model and significantly increased by DOP treatment (9.6 g/kg). Conclusions. These findings not only showed DOP inhibits PLGC development by upregulating the PER3 and AQP4 gene and protein expression but also suggested that its mechanism of action involved modulating the Circadian Rhythm Signaling pathway.</abstract><cop>United States</cop><pub>Hindawi</pub><pmid>34721627</pmid><doi>10.1155/2021/3036504</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9692-0562</orcidid><orcidid>https://orcid.org/0000-0002-9633-646X</orcidid><orcidid>https://orcid.org/0000-0002-5449-8428</orcidid><orcidid>https://orcid.org/0000-0003-1995-6144</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Aquaporin 4 Binding sites Chinese medicine Circadian rhythms Computer programs Dendrobium officinale Drug dosages Evidence-based medicine Gastric cancer Gene expression Laboratory animals Nonsteroidal anti-inflammatory drugs Pancreatic cancer Period 3 protein Polymerase chain reaction Polysaccharides Protein expression Proteins Signal transduction Software Traditional Chinese medicine Variance analysis |
title | RNA-Seq Analysis Reveals Dendrobium officinale Polysaccharides Inhibit Precancerous Lesions of Gastric Cancer through PER3 and AQP4 |
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