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Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation
BACKGROUND: The microRNA‐371a‐3p (miR‐371a‐3p) has been reported to be an informative liquid biopsy (serum and plasma) molecular biomarker for both diagnosis and follow‐up of patients with a malignant (testicular) germ cell tumor ((T)GCT). It is expressed in all histological cancer elements, with th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767197/ https://www.ncbi.nlm.nih.gov/pubmed/30786164 http://dx.doi.org/10.1111/andr.12595 |
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author | Boellaard, W. P. A. Gillis, A. J. M. van Leenders, G. J. L. H. Stoop, H. van Agthoven, T. Dorssers, L. C. J. Dinkelman‐Smit, M. Boormans, J. L. Looijenga, L. H. J. |
author_facet | Boellaard, W. P. A. Gillis, A. J. M. van Leenders, G. J. L. H. Stoop, H. van Agthoven, T. Dorssers, L. C. J. Dinkelman‐Smit, M. Boormans, J. L. Looijenga, L. H. J. |
author_sort | Boellaard, W. P. A. |
collection | PubMed |
description | BACKGROUND: The microRNA‐371a‐3p (miR‐371a‐3p) has been reported to be an informative liquid biopsy (serum and plasma) molecular biomarker for both diagnosis and follow‐up of patients with a malignant (testicular) germ cell tumor ((T)GCT). It is expressed in all histological cancer elements, with the exception of mature teratoma. However, normal testis, semen, and serum of males with a disrupted testicular integrity without a TGCT may contain miR‐371a‐3p levels above threshold, of which the cellular origin is unknown. OBJECTIVES: Therefore, a series of relevant tissues (frozen and formalin‐fixed paraffin‐embedded (FFPE), when available) from the complete male urogenital tract (i.e., kidney to urethra and testis to urethra) and semen was investigated for miR‐371a‐3p levels using targeted quantitative RT‐PCR (qRT‐PCR). MATERIALS AND METHODS: In total, semen of males with normospermia (n = 11) and oligospermia (n = 3) was investigated, as well as 88 samples derived from 32 different patients. The samples represented one set of tissues related to the entire male urogenital tract (11 anatomical locations), three sets for 10 locations, and four sets for six locations. RESULTS: All testis parenchyma (n = 17) cases showed low miR‐371a‐3p levels. Eight out of 14 (57%) semen samples showed detectable miR‐371a‐3p levels, irrespective of the amount of motile spermatozoa, but related to sperm concentration and matched Johnsen score (Spearman's rho correlation coefficient 0.849 and 0.871, p = 0.000, respectively). In all other tissues investigated, miR‐371a‐3p could not be detected. DISCUSSION: This study demonstrates that the miR‐371a‐3p in healthy adult males is solely derived from the germ cell compartment. CONCLUSIONS: The observation is important in the context of applying miR‐371a‐3p as molecular liquid biopsy biomarker for diagnosis and follow‐up of patients with malignant (T)GCT. Moreover, miR‐371a‐3p might be an informative seminal biomarker for testicular germ cell composition. |
format | Online Article Text |
id | pubmed-6767197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67671972019-10-03 Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation Boellaard, W. P. A. Gillis, A. J. M. van Leenders, G. J. L. H. Stoop, H. van Agthoven, T. Dorssers, L. C. J. Dinkelman‐Smit, M. Boormans, J. L. Looijenga, L. H. J. Andrology Original Articles BACKGROUND: The microRNA‐371a‐3p (miR‐371a‐3p) has been reported to be an informative liquid biopsy (serum and plasma) molecular biomarker for both diagnosis and follow‐up of patients with a malignant (testicular) germ cell tumor ((T)GCT). It is expressed in all histological cancer elements, with the exception of mature teratoma. However, normal testis, semen, and serum of males with a disrupted testicular integrity without a TGCT may contain miR‐371a‐3p levels above threshold, of which the cellular origin is unknown. OBJECTIVES: Therefore, a series of relevant tissues (frozen and formalin‐fixed paraffin‐embedded (FFPE), when available) from the complete male urogenital tract (i.e., kidney to urethra and testis to urethra) and semen was investigated for miR‐371a‐3p levels using targeted quantitative RT‐PCR (qRT‐PCR). MATERIALS AND METHODS: In total, semen of males with normospermia (n = 11) and oligospermia (n = 3) was investigated, as well as 88 samples derived from 32 different patients. The samples represented one set of tissues related to the entire male urogenital tract (11 anatomical locations), three sets for 10 locations, and four sets for six locations. RESULTS: All testis parenchyma (n = 17) cases showed low miR‐371a‐3p levels. Eight out of 14 (57%) semen samples showed detectable miR‐371a‐3p levels, irrespective of the amount of motile spermatozoa, but related to sperm concentration and matched Johnsen score (Spearman's rho correlation coefficient 0.849 and 0.871, p = 0.000, respectively). In all other tissues investigated, miR‐371a‐3p could not be detected. DISCUSSION: This study demonstrates that the miR‐371a‐3p in healthy adult males is solely derived from the germ cell compartment. CONCLUSIONS: The observation is important in the context of applying miR‐371a‐3p as molecular liquid biopsy biomarker for diagnosis and follow‐up of patients with malignant (T)GCT. Moreover, miR‐371a‐3p might be an informative seminal biomarker for testicular germ cell composition. John Wiley and Sons Inc. 2019-02-20 2019-07 /pmc/articles/PMC6767197/ /pubmed/30786164 http://dx.doi.org/10.1111/andr.12595 Text en © 2019 The Authors. Andrology published by John Wiley & Sons Ltd on behalf of American Society of Andrology and European Academy of Andrology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Boellaard, W. P. A. Gillis, A. J. M. van Leenders, G. J. L. H. Stoop, H. van Agthoven, T. Dorssers, L. C. J. Dinkelman‐Smit, M. Boormans, J. L. Looijenga, L. H. J. Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
title | Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
title_full | Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
title_fullStr | Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
title_full_unstemmed | Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
title_short | Cellular origin of microRNA‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
title_sort | cellular origin of microrna‐371a‐3p in healthy males based on systematic urogenital tract tissue evaluation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767197/ https://www.ncbi.nlm.nih.gov/pubmed/30786164 http://dx.doi.org/10.1111/andr.12595 |
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