Evidence map›Paper›PMID 32708730›Full record

ArticleCells2020

CXCL14 Maintains hESC Self-Renewal through Binding to IGF-1R and Activation of the IGF-1R Pathway.

Chih-Lun Cheng, Shang-Chih Yang, Chien-Ying Lai, Cheng-Kai Wang, Ching-Fang Chang, Chun-Yu Lin, Wei-Ju Chen, Po-Yu Lin, Han-Chung Wu, Nianhan Ma and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. The role of IGF/IGF-1R signaling in the regulation of cancer stem cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Review
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

12 authors at 6 institutions in 1 country.

Chih-Lun ChengGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.
Shang-Chih YangGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Chien-Ying LaiGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Cheng-Kai WangGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Ching-Fang ChangGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Chun-Yu LinGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Wei-Ju ChenGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Po-Yu LinGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Han-Chung WuGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.
Nianhan MaDepartment of Biomedical Sciences and Engineering, National Central University, Taoyuan City 320, Taiwan.
Frank Leigh LuDepartment of Pediatrics, National Taiwan University Children's Hospital, National Taiwan University Hospital, and National Taiwan University Medical College, Taipei 100, Taiwan.ORCID 0000-0002-5225-7751
Jean LuGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan.
Genomics Research Center, Academia Sinica · TWNational Yang Ming Chiao Tung University · TWInstitute of Cellular and Organismic Biology, Academia Sinica · TWNational Central University · TWNational Taiwan University · TWNational Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human embryonic stem cells (hESCs) have important roles in regenerative medicine, but only a few studies have investigated the cytokines secreted by hESCs. We screened and identified chemokine (C-X-C motif) ligand 14 (CXCL14), which plays crucial roles in hESC renewal. CXCL14, a C-X-C motif chemokine, is also named as breast and kidney-expressed chemokine (BRAK), B cell and monocyte-activated chemokine (BMAC), and macrophage inflammatory protein-2γ (MIP-2γ). Knockdown of

Indexed as

Cell Self RenewalSignal TransductionCell CycleCell DifferentiationCell LineChemokines, CXCGene Knockdown TechniquesHuman Embryonic Stem CellsHumansModels, BiologicalProtein BindingReceptor, IGF Type 1RNA, Small InterferingChemokines, CXCCXCL14 protein, humanIGF1R protein, humanReceptor, IGF Type 1RNA, Small InterferingBMACBRAKcell cycleCXCL14human embryonic stem cellIGF-1RMip-2γself-renewal

Identifiers

PMID32708730
PMCPMC7407311
OpenAlexW3043593485

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.