Evidence map›Paper›PMID 26886608›Full record

ArticleMedicine2016

Targeted Disruption of miR-17-92 Impairs Mouse Spermatogenesis by Activating mTOR Signaling Pathway.

Raoying Xie, Xiaolin Lin, Tao Du, Kang Xu, Hongfen Shen, Fang Wei, Weichao Hao, Taoyan Lin, Xia Lin, Yujuan Qin and 9 more

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
4.2field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Small RNAs, spermatogenesis, and male infertility: a decade of retrospect.Reproductive biology and endocrinology : RB&E · 2023
    Review
  11. Frontiers in cell and developmental biology · 2023
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Regulation of mammalian spermatogenesis by miRNAs.Seminars in cell & developmental biology · 2022
    Review
  17. MiR-181a Promotes Spermatogenesis by Targeting the S6K1 Pathway.International journal of stem cells · 2021
    Article
  18. Article
  19. Article
  20. Article
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

19 authors at 1 institution in 5 countries.

Raoying XieFrom the Cancer Research Institute, Southern Medical University (RX, XL, HS, FW, WH, TL, XL, YQ, HW, LC, SY, JY, KY, DX, JJ); Institute of Comparative Medicine and Laboratory Animal Center, Southern Medical University (RX, DX); Zhongshan School of Medicine, Sun Yat-sen University (YS); Department of Endocrinology, The Second Affiliated Hospital, Guangzhou Medical University (TD); Department of General Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou (KX); Department of Chemoradiotherapy, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou (RX); Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University (KX); Department of Oncology, Nanfang Hospital, Southern Medical University (XR); and Guangzhou Digestive Disease Center, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China (FW).
Xiaolin Lin
Tao Du
Kang Xu
Hongfen Shen
Fang Wei
Weichao Hao
Taoyan Lin
Xia Lin
Yujuan Qin
Huiyan Wang
Lin Chen
Sheng Yang
Jie Yang
Xiaoxiang Rong
Kaitai Yao
Dong Xiao
Junshuang Jia
Yan Sun
National Natural Science Foundation of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The miR-17-92 cluster and its 6 different mature microRNAs, including miR-17, miR-18a, miR-19a, miR-20a, miR-19b-1, and miR-92a, play important roles in embryo development, immune system, kidney and heart development, adipose differentiation, aging, and tumorigenicity. Currently, increasing evidence indicates that some members of miR-17-92 cluster may be critical players in spermatogenesis, including miR-17, miR-18a, and miR-20a. However, the roles and underlying mechanisms of miR-17-92 in spermatogenesis remain largely unknown. Our results showed that the targeted disruption of miR-17-92 in the testes of adult mice resulted in severe testicular atrophy, empty seminiferous tubules, and depressed sperm production. This phenotype is partly because of the reduced number of spermatogonia and spermatogonial stem cells, and the significantly increased germ cell apoptosis in the testes of miR-17-92-deficient mice. In addition, overactivation of the mammalian target of rapamycin signaling pathway and upregulation of the pro-apoptotic protein Bim, Stat3, c-Kit, and Socs3 were also observed in miR-17-92-deficient mouse testes, which might be, at least partially if not all, responsible for the aforementioned phenotypic changes in mutant testes. Taken together, these findings suggest that miR-17-92 is essential for normal spermatogenesis in mice.

Indexed as

AnimalsApoptosisApoptosis Regulatory ProteinsBcl-2-Like Protein 11Cell LineMaleMembrane ProteinsMiceMicroRNAsProto-Oncogene ProteinsSignal TransductionSpermatogenesisSpermatogoniaTestisTOR Serine-Threonine KinasesApoptosis Regulatory ProteinsBcl2l11 protein, mouseBcl-2-Like Protein 11Membrane ProteinsMicroRNAsMIRN17-92 microRNA, mouseProto-Oncogene ProteinsTOR Serine-Threonine Kinases

Identifiers

PMID26886608
PMCPMC4998608
OpenAlexW2319235871

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.