Epitranscriptomics has
gained ground in recent years, especially after the advent of techniques for
accurately studying these mechanisms. Among all modifications occurring in RNA
molecules, N6-methyladenosine (m⁶A) is
the most frequent, especially among mRNAs. m⁶A has
been demonstrated to play important roles in many physiological procedure and
several disease states, including various cancer models (from solid
to liquid tumors). Tumor cells' epitranscriptome is indeed disrupted in a way
to promote cancer-prone features, by means of up/downregulating m⁶A-related players: the so-called writers, readers
and erasers. These proteins modulate m⁶A
establishment, removal and determine mRNAs fate, acting in a context-dependent
manner, so that a single player may act as an oncogenic signal in one tumor
model (methyltransferase like 3 (METTL3) in lung cancer) and as a tumor
suppressor in another context (METTL3 in glioblastoma). Despite recent
advances, however, little attention has been directed towards urological cancer.
By means of a thorough analysis of the publicly available TCGA (The Cancer Genome
Atlas) database, we disclosed the most relevant players in four major
urogenital neoplasms-kidney, bladder, prostate and testicular cancer-for
prognostic, subtype discrimination and survival purposes. In all tumor models
assessed, the most promising player was shown to be Vir like m⁶A methyltransferase associated (VIRMA), which
could constitute a potential target for personalized therapies.
https://epigenetics.expertconferences.org/events-list/cancer-epigenetics-oncology
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