AI Article Synopsis

  • PIWI pathway proteins are crucial for germ cell development during spermatogenesis and their decreased expression is linked to testicular germ cell tumors (TGCTs).
  • The study focuses on examining not just normal testis and TGCT samples, but also preneoplastic testis tissues next to TGCTs, using matched samples to reduce patient variability.
  • Findings reveal that spermatogenesis remains in tissues near nonseminomas while PIWI gene expression and DNA methylation patterns differ, suggesting distinct developmental pathways for TGCT types and potential for new diagnostic markers.

Article Abstract

PIWI pathway proteins are expressed during spermatogenesis where they play a key role in germ cell development. Epigenetic loss of PIWI proteins expression was previously demonstrated in testicular germ cell tumors (TGCTs), implying their involvement in TGCT development. In this work, apart from studying only normal testis and TGCT samples, we also analyzed an intermediate stage, i.e. preneoplastic testis tissues adjacent to TGCTs. Importantly, in this study, we minimized the contribution of patient-to-patient heterogeneity by using matched preneoplastic/TGCT samples. Surprisingly, expression of germ cell marker DDX4 suggests that spermatogenesis is retained in premalignant testis tissues adjacent to nonseminoma, but not those adjacent to seminoma. Moreover, this pattern is followed by expression of PIWI pathway genes, which impacts one of their functions: DNA methylation level over LINE-1 promoters is higher in preneoplastic testis tissues adjacent to nonseminomas than those adjacent to seminomas. This finding might imply distinct routes for development of the two types of TGCTs and could be used as a novel diagnostic marker, possibly, noninvasively. Finally, we studied the role of CpG island methylation in expression of PIWI genes in patient samples and using in vitro experiments in cell line models: a more complex interrelation between DNA methylation and expression of the corresponding genes was revealed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008371PMC
http://dx.doi.org/10.18632/oncotarget.7074DOI Listing

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