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Graded expression of microRNA-371a-3p in tumor tissues, contralateral testes, and in serum of patients with testicular germ cell tumor.
Belge, Gazanfer; Hennig, Finja; Dumlupinar, Cansu; Grobelny, Francesca; Junker, Klaus; Radtke, Arlo; Dieckmann, Klaus-Peter.
  • Belge G; Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
  • Hennig F; Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
  • Dumlupinar C; Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
  • Grobelny F; Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
  • Junker K; Department of Pathology, Klinikum Bremen-Mitte, Bremen, Germany.
  • Radtke A; Faculty of Biology and Chemistry, University of Bremen, Bremen, Germany.
  • Dieckmann KP; Department of Urology, Asklepios Klinik Altona, Hamburg, Germany.
Oncotarget ; 11(16): 1462-1473, 2020 Apr 21.
Article en En | MEDLINE | ID: mdl-32363003
ABSTRACT

Background:

Serum levels of microRNA-371a-3p represent a specific tumor marker of testicular germ cell tumors (GCTs) but the origin of circulating miR-371a-3p is not finally resolved. The correlation between miR-levels in tissue and serum is unclear.

Results:

MiR-levels in GCT tissue are 399-fold higher than in contralateral testicular tissue and 5843-fold higher than in non-testicular tissue. MiR tissue levels correlate with corresponding serum levels (r 2 = 0.181). ISH detected miR-371a-3p intracellularly in GCT cells except teratoma. A low expression was also detected in normal testicular germ cells.

Conclusions:

Circulating miR-371a-3p is specifically derived from GCT tissue. The miR is present in GCT cells except teratoma. A low expression is also found in normal testicular tissue but not in non-testicular tissue. MiR-371a-3p levels in tissue and serum correlate significantly. This study underscores the usefulness of serum miR-371a-3p as tumor marker of GCT. Patients and

methods:

Expression levels of miR-371a-3p were concurrently measured in tissues of GCT, contralateral testes ( n = 38), and in serum ( n = 36) with real time PCR. For control, 5 healthy testicles and 4 non-testicular tissue samples were examined. MiR-levels were compared using descriptive statistical methods. We also performed in situ hybridization (ISH) of GCT tissue with a probe specific for miR-371a-3p.
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