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lncRNA - Long Non-coding RNAs02:39

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer
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Identification of lncRNA Signature Associated With Pan-Cancer Prognosis.

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    This study introduces a novel 5-long noncoding RNA (lncRNA) signature for predicting pan-cancer prognosis. This signature accurately stratifies patients into distinct risk groups, offering a potential tool for cancer patient management.

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    Area of Science:

    • Genomics
    • Cancer Biology
    • Bioinformatics

    Background:

    • Long noncoding RNAs (lncRNAs) are implicated in cancer development and progression.
    • A validated pan-cancer prognostic signature based on lncRNAs is currently lacking.

    Purpose of the Study:

    • To develop and validate a robust lncRNA-based prognostic signature for diverse human cancers.
    • To identify novel lncRNAs with prognostic value across multiple cancer types.

    Main Methods:

    • A framework integrating statistical power, biological rationale, and machine learning was employed.
    • A 5-lncRNA signature was identified using TCGA training data and validated in independent TARGET and CPTAC cohorts.
    • In silico functional analysis was performed to explore the biological relevance of the identified lncRNAs.

    Main Results:

    • A 5-lncRNA signature (ENSG00000206567, PCAT29, ENSG00000257989, LOC388282, LINC00339) was identified and significantly associated with overall survival (OS) in TCGA cohort.
    • The signature effectively stratified patients into low- and high-risk groups with distinct survival outcomes (log-rank P = 1.48E-38) and demonstrated good prognostic performance (AUC = 0.72 with clinical factors).
    • Validation in external cohorts confirmed the signature's prognostic value (AUCs of 0.60 and 0.75).

    Conclusions:

    • The developed 5-lncRNA signature serves as a reliable pan-cancer prognostic marker.
    • The identified lncRNAs, particularly ENSG00000257989, LOC388282, and ENSG00000206567, may represent novel therapeutic targets common across various cancers.