Evidence map›Paper›PMID 24511119›Full record

ArticleJournal of the American Society of Nephrology : JASN2014

Galectin-1 upregulates CXCR4 to promote tumor progression and poor outcome in kidney cancer.

Chang-Shuo Huang, Shye-Jye Tang, Ling-Yen Chung, Cheng-Ping Yu, Jar-Yi Ho, Tai-Lung Cha, Chii-Cheng Hsieh, Hsiao-Hsien Wang, Guang-Huan Sun, Kuang-Hui Sun

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 5 pooled it
2.7field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 5 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Clinicopathological significance of galectin-1 expression and percentage of galectin-1-expressing T cells in clear-cell renal cell carcinoma.Canadian Urological Association journal = Journal de l'Association des urologues du Canada · 2018
    Article
  18. Article
  19. Galectins as Molecular Targets for Therapeutic Intervention.International journal of molecular sciences · 2018
    Review
  20. 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

10 authors at 4 institutions in 1 country.

Chang-Shuo HuangDepartment of Biotechnology and Laboratory Science in Medicine, Infection and Immunity Center, National Yang-Ming University, Department of Education and Research, Taipei City Hospital, Taipei, Taiwan;
Shye-Jye TangInstitute of Marine Biotechnology, National Taiwan Ocean University, Keelung, Taiwan;
Ling-Yen ChungDepartment of Biotechnology and Laboratory Science in Medicine, Infection and Immunity Center, National Yang-Ming University, Department of Education and Research, Taipei City Hospital, Taipei, Taiwan;
Cheng-Ping YuBiobank Management Center, Graduate Institute of Pathology and Parasitology, and.
Jar-Yi HoBiobank Management Center, Graduate Institute of Pathology and Parasitology, and.
Tai-Lung ChaDivision of Urology, Department of Surgery, Tri-Service General Hospital and National Defense Medical Center, Taipei, Taiwan; and.
Chii-Cheng HsiehDivision of Urology, Department of Surgery, Cheng-Hsin General Hospital, Taipei, Taiwan.
Hsiao-Hsien WangDivision of Urology, Department of Surgery, Cheng-Hsin General Hospital, Taipei, Taiwan.
Guang-Huan SunDivision of Urology, Department of Surgery, Tri-Service General Hospital and National Defense Medical Center, Taipei, Taiwan; and khsun@ym.edu.tw ghsun@mail.ndmctsgh.edu.tw.
Kuang-Hui SunDepartment of Biotechnology and Laboratory Science in Medicine, Infection and Immunity Center, National Yang-Ming University, Department of Education and Research, Taipei City Hospital, Taipei, Taiwan; khsun@ym.edu.tw ghsun@mail.ndmctsgh.edu.tw.
National Yang Ming Chiao Tung University · TWCheng Hsin General Hospital · TWNational Defense Medical Center · TWNational Taiwan Ocean University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Galectin-1, a β-galactoside-binding lectin, is involved in many physiologic and pathologic processes, including cell adhesion, differentiation, angiogenesis, and tumor progression. However, the role of galectin-1 in kidney cancer remains elusive. This study evaluated the role of galectin-1 in the progression and clinical prognosis of renal cell carcinoma. We found significant overexpression of galectin-1 in both kidney cancer cell lines and metastatic tissue specimens from patients with renal cell carcinoma. Knockdown of galectin-1 gene expression in renal cancer cell lines reduced cell invasion, clonogenic ability, and epithelial-mesenchymal transition in vitro; reduced tumor outgrowth in vivo; and inhibited the angiogenesis-inducing activity of these cells in vitro and in vivo. Galectin-1 knockdown decreased CXCR4 expression levels in kidney cancer cells, and restoration of CXCR4 expression in galectin-1-silenced cells rescued cell motility and clonogenic ability. Additional studies suggested that galectin-1 induced CXCR4 expression through activation of nuclear factor-κB (NF-κB). Analysis of patient specimens confirmed the clinical significance and positive correlation between galectin-1 and CXCR4 expression levels and revealed concomitant overexpression of galectin-1 and CXCR4 associated adversely with overall and disease-free survival. Our findings suggest that galectin-1 promotes tumor progression through upregulation of CXCR4 via NF-κB. The coordinated upregulation of galectin-1 and CXCR4 may be a novel prognostic factor for survival in patients with renal cell carcinoma and the galectin-1-CXCR4 axis may serve as a therapeutic target in this disease.

Indexed as

Up-RegulationCarcinoma, Renal CellDisease ProgressionGalectin 1HumansKidney NeoplasmsPrognosisReceptors, CXCR4Survival RateTumor Cells, CulturedCXCR4 protein, humanGalectin 1Receptors, CXCR4chemokine receptorrenal carcinomasurvival

Identifiers

PMID24511119
PMCPMC4073433
OpenAlexW2125481638

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.