Evidence map›Paper›PMID 28678825›Full record

ArticlePloS one2017

HMGB3 promotes growth and migration in colorectal cancer by regulating WNT/β-catenin pathway.

Zheying Zhang, Yaya Chang, Jianming Zhang, Yanxia Lu, Lin Zheng, Yuhan Hu, Fan Zhang, Xiaomin Li, Wenjuan Zhang, Xuenong Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Structure and Functions of HMGB3 Protein.International journal of molecular sciences · 2024
    Review
  13. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The expression of high mobility group protein 3 (American journal of cancer research · 2023
    Article
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 3 institutions in 1 country.

Zheying ZhangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yaya ChangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Jianming ZhangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yanxia LuDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Lin ZhengDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yuhan HuDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Fan ZhangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Xiaomin LiDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Wenjuan ZhangDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Xuenong LiDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.ORCID http://orcid.org/0000-0003-1535-0735
Southern Medical University · CNCapital Medical University · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the third leading cause of cancer-related deaths and a major health problem. High mobility group box 3 (HMGB3), a member of the high-mobility group box (HMGB) family, was reported to be over-expressed in gastric carcinoma and bladder cancer. However, the function of HMGB3 in CRC remains unclear. Here, we found that HMGB3 was up-regulated in CRC at both mRNA and protein levels. qRT-PCR results showed that high expression of HMGB3 had positive correlation with serosal invasion, lymph metastasis, and tumor-node-metastasis (TNM) stage in CRC patient. Functional experiments showed that HMGB3 can promote CRC cells proliferation and migration in vitro. Moreover, we found HMGB3 can active WNT/β-catenin pathway to increase the expression level of c-Myc and MMP7. These results may be the reason for HMGB3 oncogene role in CRC. In summary, our data indicated that HMGB3 may serve as an oncoprotein and could be used as a potential prognostic marker in CRC.

Indexed as

Cell MovementWnt Signaling PathwayCell Line, TumorCell ProliferationColonColorectal NeoplasmsDisease ProgressionFemaleGene ExpressionGene Expression Regulation, NeoplasticHMGB3 ProteinHumansLymphatic MetastasisMaleMiddle AgedHMGB3 Protein

Identifiers

PMID28678825
PMCPMC5497964
OpenAlexW2725646060

What OpenQuestion holds

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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.