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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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