Evidence map›Paper›PMID 27806345›Full record

ArticleOncotarget2016

ING4 suppresses tumor angiogenesis and functions as a prognostic marker in human colorectal cancer.

Yansu Chen, Yefei Huang, Pingfu Hou, Zhe Zhang, Yafei Zhang, Weimin Wang, Guixiang Sun, Lichun Xu, Jianwei Zhou, Jin Bai and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. New insights into the role of ubiquitination in angiogenesis (Review).International journal of molecular medicine · 2025
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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

11 authors at 3 institutions in 1 country.

Yansu ChenJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Yefei HuangJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Pingfu HouJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Zhe ZhangJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Yafei ZhangJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Weimin WangDepartment of Oncology, Yixing People's Hospital, Yixing 214200, Jiangsu Province, China.
Guixiang SunSchool of Public Health, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Lichun XuSchool of Public Health, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Jianwei ZhouDepartment of Molecular Cell Biology and Toxicology, Cancer Center, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.
Jin BaiJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Junnian ZhengJiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical University, Xuzhou 221002, Jiangsu Province, China.
Xuzhou Medical College · CNJiangsu University · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ING4, a potential tumor suppressor, is implicated in cell cycle arrest, apoptosis, cell migration and angiogenesis. Here, we investigated the clinical value of ING4 and its impact on angiogenesis in colorectal cancer (CRC). In this study, we found that ING4 expression was significantly reduced in CRC tissues versus paired normal colon tissues. Moreover, low ING4 expression was significantly associated with increased lymph node metastasis, advanced TNM stage and poor overall survival. Multivariate Cox regression analysis showed that ING4 expression was an independent favourable prognostic factor for CRC (hazard ratio = 0.45, P = 0.001). In addition, we found that ING4 strongly inhibited CRC angiogenesis by suppressing Sp1 expression and transcriptional activity through ubiquitin degradation and down-regulating the expressions of Sp1 downstream pro-angiogenic genes, MMP-2 and COX-2. Moreover, ING4 might inhibit phosphorylation activity of cyclin/CDK2 complexes to trigger Sp1 degradation by inducing p21 expression in despite of p53 status. Our findings imply that reduced ING4 expression in CRC resulted in increased angiogenesis and contributed to CRC metastasis and poor prognosis. Restoration of ING4 may be a novel strategy for the treatment of metastatic CRC.

Indexed as

AnimalsBiomarkers, TumorCell Cycle ProteinsCell Line, TumorColorectal NeoplasmsCyclin-Dependent Kinase Inhibitor p21Cyclooxygenase 2Down-RegulationFemaleGene Expression Regulation, NeoplasticHCT116 CellsHomeodomain ProteinsHumansMaleMatrix Metalloproteinase 2MiceBiomarkers, TumorCDKN1A protein, humanCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p21Cyclooxygenase 2Homeodomain ProteinsING4 protein, humanMatrix Metalloproteinase 2MMP2 protein, humanPTGS2 protein, humanSP1 protein, humanSp1 Transcription FactorTumor Suppressor Proteinsangiogenesiscolorectal cancerING4prognosisSp1

Identifiers

PMID27806345
PMCPMC5346695
OpenAlexW2542277100

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.