Evidence map›Paper›PMID 28424251›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Nuclear Shp2 directs normal embryo implantation via facilitating the ERα tyrosine phosphorylation by the Src kinase.

Hao Ran, Shuangbo Kong, Shuang Zhang, Jianghong Cheng, Chan Zhou, Bo He, Qiliang Xin, John P Lydon, Francesco J DeMayo, Gen-Sheng Feng and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

  1. Trial
  2. Article
  3. WT1 directs normal progesterone receptor-chromatin binding essential for uterine receptivity at peri-implantation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
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  8. Basic Research Advances in China on Embryo Implantation, Placentation, and Parturition.Maternal-fetal medicine (Wolters Kluwer Health, Inc.) · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. A comprehensive review of SHP2 and its role in cancer.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review
  13. Article
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  15. Review
  16. Article
  17. Article
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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

14 authors at 8 institutions in 2 countries.

Hao RanState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing 100193, People's Republic of China.
Shuangbo KongReproductive Medical Center, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian 361003, People's Republic of China.
Shuang ZhangState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing 100101, People's Republic of China.
Jianghong ChengSchool of Pharmaceutical Sciences, State Key Laboratory of Cellular Stress Biology, Xiamen University, Xiamen, Fujian 361005, People's Republic of China.
Chan ZhouState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing 100193, People's Republic of China.
Bo HeFujian Provincial Key Laboratory of Reproductive Health Research, Medical College of Xiamen University, Xiamen, Fujian 361102, People's Republic of China.
Qiliang XinState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing 100193, People's Republic of China.
John P LydonDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030.
Francesco J DeMayoPregnancy and Female Reproduction Group, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
Gen-Sheng FengDepartment of Pathology, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093-0864.
Guoliang XiaState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing 100193, People's Republic of China.
Zhongxian LuSchool of Pharmaceutical Sciences, State Key Laboratory of Cellular Stress Biology, Xiamen University, Xiamen, Fujian 361005, People's Republic of China; haibin.wang@vip.163.com zhongxian@xmu.edu.cn wangcam@cau.edu.cn.
Chao WangState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing 100193, People's Republic of China; haibin.wang@vip.163.com zhongxian@xmu.edu.cn wangcam@cau.edu.cn.
Haibin WangReproductive Medical Center, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian 361003, People's Republic of China; haibin.wang@vip.163.com zhongxian@xmu.edu.cn wangcam@cau.edu.cn.
China Agricultural University · CNXiamen University · CNFujian Medical University · CNBaylor College of Medicine · USInstitute of Zoology · CNNational Institute of Environmental Health Sciences · USUniversity of California, San Diego · USUniversity of Chinese Academy of Sciences · CN

Funding

Environmental Signaling in Reproduction and PregnancyZIAES103311 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI DEMAYO, FRANCESCO · 2016 to 2025
$30.5M
6 · The paper itself

Abstract

Estrogen and progesterone coupled with locally produced signaling molecules are essential for embryo implantation. However, the hierarchical landscape of the molecular pathways that governs this process remains largely unexplored. Here we show that the protein tyrosine phosphatase Shp2, a positive transducer of RTK signaling, is predominately localized in the nuclei in the periimplantation mouse uterus. Uterine-specific deletion of Shp2 exhibits reduced progesterone receptor (PR) expression and progesterone resistance, which derails normal uterine receptivity, leading to complete implantation failure in mice. Notably, the PR expression defects are attributed to the limited estrogen receptor α (ERα) activation in uterine stroma. Further analysis reveals that nuclear Shp2, rather than cytosolic Shp2, promotes the ERα transcription activity. This function is achieved by enhancing the Src kinase-mediated ERα tyrosine phosphorylation, which facilitates ERα binding to

Indexed as

AnimalsCell LineCell NucleusEmbryo ImplantationEstrogen Receptor alphaFemaleHumansMiceMice, TransgenicPhosphorylationPregnancyProtein Tyrosine Phosphatase, Non-Receptor Type 11src-Family KinasesUterusEstrogen Receptor alphaProtein Tyrosine Phosphatase, Non-Receptor Type 11Ptpn11 protein, mousesrc-Family KinasesERK signalingestrogen receptorShp2Src kinaseuterine receptivity

Identifiers

PMID28424251
PMCPMC5422785
OpenAlexW2606004982

What OpenQuestion holds

Textmetadata
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.