Evidence map›Paper›PMID 34359947›Full record

ReviewCells2021

Cellular Therapy via Spermatogonial Stem Cells for Treating Impaired Spermatogenesis, Non-Obstructive Azoospermia.

Nesma E Abdelaal, Bereket Molla Tanga, Mai Abdelgawad, Sahar Allam, Mostafa Fathi, Islam M Saadeldin, Seonggyu Bang, Jongki Cho

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  16. Germline stem cells in human.Signal transduction and targeted therapy · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 7 institutions in 4 countries.

Nesma E AbdelaalInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Universite Paris-Saclay/Île-de-France, 91198 Gif-sur-Yvette, France.
Bereket Molla TangaCollege of Veterinary Medicine, Chungnam National University, Daejeon 34134, Korea.
Mai AbdelgawadBiotechnology and Life Sciences Department, Faculty of Postgraduate Studies for Advanced Sciences (PSAS), Beni-Suef University, Beni-Suef 62521, Egypt.ORCID 0000-0003-0884-4235
Sahar AllamFaculty of Medicine, Tanta University, Tanta 31527, Egypt.ORCID 0000-0002-1038-0444
Mostafa FathiBiotechnology Program, Faculty of Agriculture, Ain Shams University, Giza 11566, Egypt.
Islam M SaadeldinDepartment of Physiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.ORCID 0000-0002-7633-730X
Seonggyu BangCollege of Veterinary Medicine, Chungnam National University, Daejeon 34134, Korea.
Jongki ChoCollege of Veterinary Medicine, Chungnam National University, Daejeon 34134, Korea.ORCID 0000-0002-8431-0457
Chungnam National University · KRAin Shams University · EGBeni-Suef University · EGCentre National de la Recherche Scientifique · FRHawassa University · ETTanta University · EGZagazig University · EG

Funding

National Research Foundation of Korea 2021R1A2C2009294
6 · The paper itself

Abstract

Male infertility is a major health problem affecting about 8-12% of couples worldwide. Spermatogenesis starts in the early fetus and completes after puberty, passing through different stages. Male infertility can result from primary or congenital, acquired, or idiopathic causes. The absence of sperm in semen, or azoospermia, results from non-obstructive causes (pretesticular and testicular), and post-testicular obstructive causes. Several medications such as antihypertensive drugs, antidepressants, chemotherapy, and radiotherapy could lead to impaired spermatogenesis and lead to a non-obstructive azoospermia. Spermatogonial stem cells (SSCs) are the basis for spermatogenesis and fertility in men. SSCs are characterized by their capacity to maintain the self-renewal process and differentiation into spermatozoa throughout the male reproductive life and transmit genetic information to the next generation. SSCs originate from gonocytes in the postnatal testis, which originate from long-lived primordial germ cells during embryonic development. The treatment of infertility in males has a poor prognosis. However, SSCs are viewed as a promising alternative for the regeneration of the impaired or damaged spermatogenesis. SSC transplantation is a promising technique for male infertility treatment and restoration of spermatogenesis in the case of degenerative diseases such as cancer, radiotherapy, and chemotherapy. The process involves isolation of SSCs and cryopreservation from a testicular biopsy before starting cancer treatment, followed by intra-testicular stem cell transplantation. In general, treatment for male infertility, even with SSC transplantation, still has several obstacles. The efficiency of cryopreservation, exclusion of malignant cells contamination in cancer patients, and socio-cultural attitudes remain major challenges to the wider application of SSCs as alternatives. Furthermore, there are limitations in experience and knowledge regarding cryopreservation of SSCs. However, the level of infrastructure or availability of regulatory approval to process and preserve testicular tissue makes them tangible and accurate therapy options for male infertility caused by non-obstructive azoospermia, though in their infancy, at least to date.

Indexed as

Cell- and Tissue-Based TherapyAdult Germline Stem CellsAzoospermiaHumansInfertility, MaleMaleSpermatogenesisStem Cell Transplantationinfertilitymalespermatogenesisspermatogonial stem cells

Identifiers

PMID34359947
PMCPMC8304133
OpenAlexW3178932016

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.