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We began analyzing https://translational-medicine.biomedcentral.com/articles/10.1186/s12967-025-06650-9, but it redirected us to https://translational-medicine.biomedcentral.com/articles/10.1186/s12967-025-06650-9. The analysis below is for the second page.

Title[redir]:
LINC02888 promotes HGSOC progression and immune evasion via PPIB-mediated stabilization of LAPTM5 mRNA and inhibition of RIG-I-like receptor signaling | Journal of Translational Medicine | Full Text
Description:
Background High-grade serous ovarian cancer (HGSOC) remains highly lethal due to late diagnosis and chemoresistance. Long noncoding RNAs (lncRNAs) have emerged as critical regulators of tumor progression. This study investigates the role of the cytoplasmic lncRNA LINC02888 in HGSOC. Methods We identified overexpression of LINC02888 in HGSOC tissues and cell lines through whole-transcriptome sequencing, qPCR, in situ hybridization, and analyses of TCGA/GTEx datasets. Functional assays including CCK-8, EdU, colony formation, wound healing, Transwell migration/invasion, and flow cytometry were performed after modulating LINC02888 expression. RNA pull-down coupled with mass spectrometry identified the RNA-binding protein PPIB as an interactor of LINC02888. RNA-seq following both LINC02888 and PPIB knockdown, along with Western blot, qPCR analyses and functional assays, revealed that LAPTM5 is a downstream effector. Furthermore, RIP-qPCR, deletion mapping, and ActD assays confirmed that LINC02888 binds PPIB, which stabilizes LAPTM5 mRNA via its 3’UTR. The effect on the RIG-I–like receptor pathway was evaluated by measuring the expression levels of RIG-I, IRF7, and ISG15. Finally, in vivo, the critical role of the LINC02888/PPIB/ LAPTM5 axis in ovarian tumor progression were explored by axillary subcutaneous injection of specifically transfected OVCAR3 cells into nude mice. Results LINC02888 was significantly upregulated in HGSOC tissues and correlated with advanced disease and poor prognosis. Silencing LINC02888 inhibited proliferation, migration, and invasion, while inducing apoptosis; conversely, overexpression promoted these oncogenic behaviors. Mechanistically, LINC02888 interacts with PPIB to stabilize LAPTM5 mRNA via its 3’UTR, resulting in elevated LAPTM5 protein levels and suppression of RIG-I–like receptor signaling. Rescue experiments confirmed the critical role of the LINC02888–PPIB–LAPTM5 axis in HGSOC progression in vivo and vitro. Conclusions Our findings reveal that LINC02888 drives HGSOC progression through a mechanism involving PPIB-mediated stabilization of LAPTM5 mRNA, which suppresses RIG-I–like receptor signaling. It also appropriately suggests that inhibiting this innate immune pathway may contribute to an immunosuppressive tumor microenvironment, making the LINC02888–PPIB–LAPTM5 axis a promising therapeutic target for this aggressive malignancy. Graphical Abstract

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šŸ™ļø Massive Traffic: 50M - 100M visitors per month


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Keywords {šŸ”}

linc, cells, ppib, laptm, hgsoc, cell, fig, pubmed, skov, ovcar, rna, overexpression, article, knockdown, mrna, google, scholar, expression, ovarian, anglne, analysis, cancer, assays, assay, central, cas, receptor, rigilike, usa, protein, data, qpcr, pathway, proliferation, experiments, scale, significantly, bar, immune, lncrnas, size, tumor, china, lncrna, migration, performed, min, revealed, levels, binding,

Topics {āœ’ļø}

gov/ccg/research/genome-sequencing/tcga mir-489-3p/dnmt3a signaling axis lncrna-mediated post-transcriptional regulation 5–15% sds-page gels a20-mediated nlrp3 deubiquitination tlr4-induced ros signaling biology-driven therapy advances glucose-induced linc01419 reprograms additional information publisher' wwp2-pten-akt pathway hormone-responsive breast cancer regulate e-cadherin expression full size image biotin-labeled linc02888 probe sars-cov-2 infection human rna-binding proteins anti-flag antibody detected normal ovarian tissue paraffin-embedded tissue sections anti-dig-biotin antibody full-length laptm5 transcript epithelial ovarian cancer receptor pathway-related proteins linc02888-driven hgsoc progression tumor-inhibitory effects induced resulting double-stranded cdna streptavidin-coated magnetic beads privacy choices/manage cookies additional plasmid constructs regulate pre-mrna splicing biotin-labeled probes agarose gel electrophoresis patient-derived xenografts linc02888/ppib/ laptm5 axis linc02888–ppib–laptm5 axis linc02888/ppib/laptm5 axis linc02888-ppib-laptm5 axis si-ppib significantly reduced ovarian tissue samples dig‐labeled linc02888 probe high-glucose dmem host-matched control igg xenograft models support chemiluminescence imaging system laptm5 mediates immature bmc ovarian tumor progression standard culture conditions larger tumor size rna-binding protein ppib

Schema {šŸ—ŗļø}

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      headline:LINC02888 promotes HGSOC progression and immune evasion via PPIB-mediated stabilization of LAPTM5 mRNA and inhibition of RIG-I-like receptor signaling
      description:High-grade serous ovarian cancer (HGSOC) remains highly lethal due to late diagnosis and chemoresistance. Long noncoding RNAs (lncRNAs) have emerged as critical regulators of tumor progression. This study investigates the role of the cytoplasmic lncRNA LINC02888 in HGSOC. We identified overexpression of LINC02888 in HGSOC tissues and cell lines through whole-transcriptome sequencing, qPCR, in situ hybridization, and analyses of TCGA/GTEx datasets. Functional assays including CCK-8, EdU, colony formation, wound healing, Transwell migration/invasion, and flow cytometry were performed after modulating LINC02888 expression. RNA pull-down coupled with mass spectrometry identified the RNA-binding protein PPIB as an interactor of LINC02888. RNA-seq following both LINC02888 and PPIB knockdown, along with Western blot, qPCR analyses and functional assays, revealed that LAPTM5 is a downstream effector. Furthermore, RIP-qPCR, deletion mapping, and ActD assays confirmed that LINC02888 binds PPIB, which stabilizes LAPTM5 mRNA via its 3’UTR. The effect on the RIG-I–like receptor pathway was evaluated by measuring the expression levels of RIG-I, IRF7, and ISG15. Finally, in vivo, the critical role of the LINC02888/PPIB/ LAPTM5 axis in ovarian tumor progression were explored by axillary subcutaneous injection of specifically transfected OVCAR3 cells into nude mice. LINC02888 was significantly upregulated in HGSOC tissues and correlated with advanced disease and poor prognosis. Silencing LINC02888 inhibited proliferation, migration, and invasion, while inducing apoptosis; conversely, overexpression promoted these oncogenic behaviors. Mechanistically, LINC02888 interacts with PPIB to stabilize LAPTM5 mRNA via its 3’UTR, resulting in elevated LAPTM5 protein levels and suppression of RIG-I–like receptor signaling. Rescue experiments confirmed the critical role of the LINC02888–PPIB–LAPTM5 axis in HGSOC progression in vivo and vitro. Our findings reveal that LINC02888 drives HGSOC progression through a mechanism involving PPIB-mediated stabilization of LAPTM5 mRNA, which suppresses RIG-I–like receptor signaling. It also appropriately suggests that inhibiting this innate immune pathway may contribute to an immunosuppressive tumor microenvironment, making the LINC02888–PPIB–LAPTM5 axis a promising therapeutic target for this aggressive malignancy.
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         name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
         type:PostalAddress
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            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
               type:PostalAddress
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      name:YanFeng Yang
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            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
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      name:DanBo Geng
      affiliation:
            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
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      name:ZiTeng Kuang
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            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
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      name:TianLi Mu
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            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
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      name:YuXi Liu
      affiliation:
            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
               type:PostalAddress
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      name:Bo Ren
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            name:Shengjing Hospital of China Medical University
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               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
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      affiliation:
            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
               type:PostalAddress
            type:Organization
      name:XiaoWei Zhang
      affiliation:
            name:Shengjing Hospital of China Medical University
            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
               type:PostalAddress
            type:Organization
      name:YuCi Zhang
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            name:The University of British Columbia
            address:
               name:Department of Computer, The University of British Columbia, Vancouver, Canada
               type:PostalAddress
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      name:Min Wang
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            address:
               name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
               type:PostalAddress
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      email:[email protected]
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      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China
      name:Department of Computer, The University of British Columbia, Vancouver, Canada
      name:Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China

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