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pmid:29320577

Genome-wide profiling of the PIWI-interacting RNA-mRNA regulatory networks in epithelial ovarian cancers.

Garima Singh · Jyoti Roy · Pratiti Rout · Bibekanand Mallick

PloS one · 2018 doi:10.1371/journal.pone.0190485

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Experiment

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Data

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Genome-wide profiling of the PIWI-interacting RNA-mRNA regulatory networks in epithelial ovarian cancers.
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10.1371/journal.pone.0190485
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Garima Singh
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Jyoti Roy
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Pratiti Rout
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Bibekanand Mallick
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PloS one
year
2018
abstract
PIWI-interacting (piRNAs), ~23-36 nucleotide-long small non-coding RNAs (sncRNAs), earlier believed to be germline-specific, have now been identified in somatic cells, including cancer cells. These sncRNAs impact critical biological processes by fine-tuning gene expression at post-transcriptional and epigenetic levels. The expression of piRNAs in ovarian cancer, the most lethal gynecologic cancer is largely uncharted. In this study, we investigated the expression of PIWILs by qRT-PCR and western blotting and then identified piRNA transcriptomes in tissues of normal ovary and two most prevalent epithelial ovarian cancer subtypes, serous and endometrioid by small RNA sequencing. We detected 219, 256 and 234 piRNAs in normal ovary, endometrioid and serous ovarian cancer samples respectively. We observed piRNAs are encoded from various genomic regions, among which introns harbor the majority of them. Surprisingly, piRNAs originated from different genomic contexts showed the varied level of conservations across vertebrates. The functional analysis of predicted targets of differentially expressed piRNAs revealed these could modulate key processes and pathways involved in ovarian oncogenesis. Our study provides the first comprehensive piRNA landscape in these samples and a useful resource for further functional studies to decipher new mechanistic views of piRNA-mediated gene regulatory networks affecting ovarian oncogenesis. The RNA-seq data is submitted to GEO database (GSE83794).
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ated the expression of PIWILs by qRT-PCR and western blotting and then identified piRNA transcriptomes in
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networks affecting ovarian oncogenesis. The RNA-seq data is submitted to GEO database (GSE83794)
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r subtypes, serous and endometrioid by small RNA sequencing. We detected 219, 256 and 234 piRNAs in norm
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Complete file
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These sncRNAs impact critical biological processes by fine-tuning gene expression at post-transcriptional and epigenetic levels. The expression of piRNAs in ovarian cancer, the most lethal gynecologic cancer is largely uncharted. In this study, we investigated the expression of PIWILs by qRT-PCR and western blotting and then identified piRNA transcriptomes in tissues of normal ovary and two most prevalent epithelial ovarian cancer subtypes, serous and endometrioid by small RNA sequencing. We detected 219, 256 and 234 piRNAs in normal ovary, endometrioid and serous ovarian cancer samples respectively. We observed piRNAs are encoded from various genomic regions, among which introns harbor the majority of them. Surprisingly, piRNAs originated from different genomic contexts showed the varied level of conservations across vertebrates. The functional analysis of predicted targets of differentially expressed piRNAs revealed these could modulate key processes and pathways involved in ovarian oncogenesis. Our study provides the first comprehensive piRNA landscape in these samples and a useful resource for further functional studies to decipher new mechanistic views of piRNA-mediated gene regulatory networks affecting ovarian oncogenesis. 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The RNA-seq data is submitted to GEO database (GSE83794)", "r subtypes, serous and endometrioid by small RNA sequencing. We detected 219, 256 and 234 piRNAs in norm", "d western blotting and then identified piRNA transcriptomes in tissues of normal ovary and two most prev"], "order_basis": "paper_text_order:597", "id": "assay:2"}, {"role": "data_generation", "definition_id": "amplicon_seq", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["opsy. The samples were stored at -80°C until next-generation sequencing, and other experiments were performed. 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All of these were related to cancer, apoptosis, cellular movement, cell cycle and cell-cell", "(LA), a well-known antioxidant that induces apoptosis by downregulating the anti-apoptotic genes ("], "order_basis": "paper_text_order:2578", "id": "assay:4"}, {"role": "data_generation", "definition_id": "microarray", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["egulation of PLEKHA5 in SOCa as evident from microarray analysis and confirmed by our qRT-PCR study"], "order_basis": "paper_text_order:9826", "id": "assay:5"}, {"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["The differential expression analysis of the small RNAs was performed using DESeq of Bioconductor [28] to obtain a set of piRNAs significantly up- or down-regulated in each of the two EOCa types with respect to normal ovary as a control."], "order_basis": "consumes_earlier_output", "id": "assay:6"}]}