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Next generation sequencing technologies to address aberrant mRNA translation in cancer.

Ángel-Carlos RománDixan A BenítezAlba Díaz-PizarroNuria Del Valle-Del PinoMarcos Olivera-GómezGuadalupe Cumplido-LasoJose M Carvajal-GonzálezSonia Mulero-Navarro
Published in: NAR cancer (2024)
In this review, we explore the transformative impact of next generation sequencing technologies in the realm of translatomics (the study of how translational machinery acts on a genome-wide scale). Despite the expectation of a direct correlation between mRNA and protein content, the complex regulatory mechanisms that affect this relationship remark the limitations of standard RNA-seq approaches. Then, the review characterizes crucial techniques such as polysome profiling, ribo-seq, trap-seq, proximity-specific ribosome profiling, rnc-seq, tcp-seq, qti-seq and scRibo-seq. All these methods are summarized within the context of cancer research, shedding light on their applications in deciphering aberrant translation in cancer cells. In addition, we encompass databases and bioinformatic tools essential for researchers that want to address translatome analysis in the context of cancer biology.
Keyphrases
  • rna seq
  • single cell
  • genome wide
  • papillary thyroid
  • copy number
  • dna methylation
  • squamous cell
  • childhood cancer
  • transcription factor
  • small molecule
  • circulating tumor
  • artificial intelligence