Evidence map›Paper›PMID 31934083›Full record

ArticleInternational journal of clinical and experimental pathology2019

IGFBP2 promotes the EMT of colorectal cancer cells by regulating E-cadherin expression.

Huange Zhu, Yanping Zhang, Yan Geng, Wei Lu, Jian Yin, Zhenzhen Li, Lun Huang, Hailong Liu, Nan Xu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The role of adipogenic niche resident cells in colorectal cancer progression in relation to obesity.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

9 authors at 1 institution in 1 country.

Huange ZhuClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Yanping ZhangClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Yan GengClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Wei LuClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Jian YinClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Zhenzhen LiClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Lun HuangClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Hailong LiuClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Nan XuClinical Laboratory, The Second Affiliated Hospital of Xi'an Jiaotong University (Xibei Hospital) Xi'an, China.
Second Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate the expression of insulin like growth factor binding protein 2 (IGFBP2) in colorectal cancer cells and its effect on the biological characteristics of cancer cells. We first established IGFBP2 knockdown (HCT116-shIGFBP2) and overexpression (HT29-IGFBP2) cell lines. Western blotting was used to evaluate the overexpression and knockdown efficiency. Next, the effect of IGFBP2 on colorectal cancer cell proliferation and migration was evaluated through cell proliferation and wound healing assays, respectively. Cell proliferation experiments showed that the upregulation of IGFBP2 promoted the proliferation of HT29 cells, but the downregulation of IGFBP2 inhibited the proliferation of HCT116 cells. Moreover, a wound healing assay showed that the migration ability of HCT116 cells was significantly reduced after the downregulation of IGFBP2. Also, the level of E-cadherin in HCT116-shIGFBP2 cells was significantly upregulated following IGFBP2 knockdown. Further analyses showed that colorectal cancer cells secreted high levels of IGFBP2 into the extracellular matrix, which inhibited E-cadherin expression as well. Overall, the results of this study showed that IGFBP2 inhibits the expression of E-cadherin and promotes the proliferation and migration of colorectal cancer cells.

Indexed as

Colorectal cancerE-cadherinepithelial-mesenchymal transition (EMT)insulin like growth factor binding protein 2 (IGFBP2)

Identifiers

PMID31934083
PMCPMC6949539
OpenAlexW3026053802

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.