Evidence map›Paper›PMID 28757546›Full record

ReviewInternational journal of molecular sciences2017

Roles of Wnt Target Genes in the Journey of Cancer Stem Cells.

Jee-Heun Kim, So-Yeon Park, Youngsoo Jun, Ji-Young Kim, Jeong-Seok Nam

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

59 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. (Journal of medicinal chemistry · 2026
    Article
  3. Article
  4. Review
  5. Evolutionary conservation and cancer implications of the WNT signaling pathway.Medical oncology (Northwood, London, England) · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
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  12. Review
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  14. Article
  15. International journal of molecular sciences · 2023
    Article
  16. A LGR5 reporter pig model closely resembles human intestine for improved study of stem cells in disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  17. Review
  18. Review
  19. 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

5 authors at 1 institution in 1 country.

Jee-Heun KimSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea. jeeheun.kim@gist.ac.kr.
So-Yeon ParkSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea. sypark0125@gist.ac.kr.
Youngsoo JunSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea. junys@gist.ac.kr.
Ji-Young KimLaboratory Animal Resource Center, Gwangju Institute of Science and Technology, Gwnagju 61005, Korea. jykim2533@gist.ac.kr.
Jeong-Seok NamSchool of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 61005, Korea. namje@gist.ac.kr.
Gwangju Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The importance of Wnt/β-catenin signaling in cancer stem cells (CSCs) has been acknowledged; however, the mechanism through which it regulates the biological function of CSCs and promotes cancer progression remains elusive. Hence, to understand the intricate mechanism by which Wnt controls stemness, the specific downstream target genes of Wnt were established by analyzing the genetic signatures of multiple types of metastatic cancers based on gene set enrichment. By focusing on the molecular function of Wnt target genes, the biological roles of Wnt were interpreted in terms of CSC dynamics from initiation to metastasis. Wnt signaling participates in cancer initiation by generating CSCs from normal stem cells or non-CSCs and augmenting persistent growth at the primary region, which is resistant to anti-cancer therapy. Moreover, it assists CSCs in invading nearby tissues and in entering the blood stream, during which the negative feedback of the Wnt signaling pathway maintains CSCs in a dormant state that is suitable for survival. When CSCs arrive at distant organs, another burst of Wnt signaling induces CSCs to succeed in re-initiation and colonization. This comprehensive understanding of Wnt target genes provides a plausible explanation for how Wnt allows CSCs variation during cancer progression.

Indexed as

Wnt Signaling PathwayCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansNeoplasmsNeoplastic Stem Cellscancer stem cellinitiationinvasionmetastasismigrationpersistenceWnt signaling

Identifiers

PMID28757546
PMCPMC5577996
OpenAlexW2738166999

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.