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. 2019 Jul 12;10:462. doi: 10.3389/fendo.2019.00462

Table 1.

Proteins identified through proteomics as putative markers in TGTC tissue.

Protein Gene Molecular function (Gene Ontology) Expressed in TGTC Biological function in TGTC Reference
Glutathione S-transferase (GSTs) M3 protein GSTM3 Protein binding Downregulated in seminoma Polymorphism of GSTM3 predict higher risk of TGCT development Zimmermann (16)
Gamma-tubulin complex component 6 GCP6 Microtubule binding Identified in seminomas but not in the normal tubules Role for microtubule nuclation at the centrosome. Excessive number of centrioles have been associated with chromosomal instability. Leman (17)
Cyclin-dependent kinase 10 CDK10 Protein binding; kinase activity Identified in seminomas but not in the normal tubules Involved in cell cycle regulation Leman (17)
StAR-related lipid transfer protein 7 STARD7 Lipid binding Absent in seminomas Involved in metabolism and signaling. It might play a role in mantaining the differentiated form of the normal cells. Leman (17)
Mab-3 doublesex- and Related Transcription Factor 1 DMTR1 Molecular function Over-expressed in mixed germ cell-sex cord stromal tumore and spermatocytic tumor Controller of mitotic proliferation of germ cells Liu (18)
Piwi-Like RNA Mediated Gene silencing 1 PIWIL1 Protein and mRNA binding Specific protein of TGCT Involved in RNA silencing during translational activity. It improves DNA methylation. Liu (18)
Transmembrane (C-Terminal) Protease, Serine 12 TMPRSS12 Serine-type endopeptidase activity Specific protein of TGTC Previously reported in prostate and liver cancer. Unknown biological mechanism. Liu (18)
p21-activated kinase 4 PAK4 Protein binding Overexpressed in embryonal carcinoma Involved in cell protections from apoptosis Castillo (19)