Global mRNA 3'UTR lengthening in small-cell neuroendocrine carcinoma

Journal: bioRxiv
Published Date:

Abstract

Small-cell neuroendocrine carcinoma (SCNC) is a rare but highly malignant tumor subtype that primarily arises in the lung, also rarely in other organs, and as a consequence of treatment induced lineage transdifferentiation of prostate adenocarcinomas. The molecular convergence of SCNC across diverse tissues enables its identification through conserved SCNC-specific molecular markers, facilitating tumor subtype classification. As a critical post-transcriptional regulatory mechanism, alternative polyadenylation (APA) modulates 3'UTR length and significantly impacts tumor progression. However, its role in SCNC remains largely unclear. Here, we report a global 3'UTR lengthening pattern driven by APA in SCNC. We identified a set of conserved 3'UTR lengthening events across SCNCs of different tissue origins, which are strongly associated with neural development and related signaling pathways. Furthermore, we developed a neural network-based prediction model to classify SCNC by leveraging these specific APA signatures. Our study provides new insights into the post-transcriptional landscape of SCNCs and highlights APA signatures as promising biomarkers for SCNC identification.

Authors

  • Zhang
  • Y.; Zhao
  • X.; Wang
  • H.; Hu
  • Y.-M.; Sun
  • X.-X.; Zhao
  • F.; Du
  • S.; Dai
  • R. S.; Andeen
  • N. K.; Sears
  • R. C.; Corey
  • E.; Brody
  • J. R.; Alumkal
  • J. J.; Mills
  • G. B.; Nelson
  • P. S.; DAI
  • M.; Xia
  • Z.

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