AI Article Synopsis

  • The study investigates the significance of autophagy-related long non-coding RNAs (lncRNAs) in predicting patient outcomes for papillary thyroid carcinoma (PTC).
  • The research analyzed data from the TCGA database, identifying 199 differentially expressed lncRNAs and creating a six-lncRNA signature to predict progression-free intervals (PFI) in patients, which outperformed traditional clinical risk assessments.
  • Results showed that patients with high-risk scores benefitted from I-131 therapy, linking these lncRNAs to better patient prognosis while revealing that they were predominantly expressed in thyroid cells.

Article Abstract

This study aimed to explore the prognostic and predictive value of autophagy-related lncRNAs in papillary thyroid carcinoma (PTC). The expression data of autophagy-related genes and lncRNAs of the PTC patients were obtained from TCGA database. Autophagy-related-differentially expressed lncRNAs (DElncs) were identified and used to establish the lncRNAs signature predicting patients' progression-free interval (PFI) in the training cohort. Its performance was assessed in the training cohort, validation cohort, and entire cohort. Effects of the signature on I-131 therapy were also explored. We identified 199 autophagy-related-DElncs and constructed a novel six-lncRNAs signature was constructed based on these lncRNAs. This signature had a good predictive performance and was superior to TNM stages and previous clinical risk scores. I-131 therapy was found to be associated with favorable prognosis in patients with high-risk scores but not those with low-risk scores. Gene set enrichment analysis suggested that a series of hallmark gene sets were enriched in the high-risk subgroup. Single-cell RNA sequencing analysis suggested that the lncRNAs were mainly expressed in thyroid cells but not stromal cells. In conclusion, our study constructed a well-performed six-lncRNAs signature to predict PFI and I-131 therapy benefits in PTC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985460PMC
http://dx.doi.org/10.1515/med-2023-0660DOI Listing

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