Evidence map›Paper›PMID 26452029›Full record

ArticleOncotarget2015

Hes1 promotes cell proliferation and migration by activating Bmi-1 and PTEN/Akt/GSK3β pathway in human colon cancer.

Fei Gao, Wei Huang, YuQin Zhang, ShaoHui Tang, Lin Zheng, Feng Ma, YiMing Wang, Hui Tang, Xin Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-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

31 citing papers in PubMed, 50 citations in OpenAlex.

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  14. Components ofJournal of oncology · 2022
    Article
  15. Long noncoding RNA MGC27382 inhibits proliferation and metastasis of non-small cell lung cancer cells via down-regulating AKT/GSK3β pathway.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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

9 authors at 2 institutions in 1 country.

Fei GaoDepartment of Gastroenterology, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Wei HuangDepartment of Gastroenterology, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
YuQin ZhangDepartment of Oncology, The First Affiliated Hospital of Jinan University, Guangzhou 510515, China.
ShaoHui TangDepartment of Gastroenterology, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Lin ZhengDepartment of Pathology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Feng MaDepartment of Gastroenterology, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
YiMing WangDepartment of Oncology, The First Affiliated Hospital of Jinan University, Guangzhou 510515, China.
Hui TangClinical Experimental Center, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Xin LiCancer Research Institute, Southern Medical University, Guangzhou 510515, China.
First Affiliated Hospital of Jinan University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hes1 is a transcription factor that influences cell proliferation and differentiation. However, the effect of Hes1 on invasiveness and the underlying mechanism remain unknown. In the current study, we found that Hes1 suppressed cell apoptosis, promoted cell growth, induced EMT phenotype and cytoskeleton reconstruction, and enhanced the metastatic potential of colon cancer cells in vitro and in vivo. Furthermore, we indicated that Bmi-1 mediated Hes1-induced cell proliferation and migration, downregulated PTEN and activated the Akt/GSK3β pathway, consequently induced EMT and cytoskeleton reconstruction, ultimately leading to enhanced invasiveness of cancer cells. In addition, we also found that both Hes1 and Bmi-1 could directly regulate PTEN by associating at the PTEN locus, and played important roles in regulating PTEN/Akt/GSK3β pathway. Our results provide functional and mechanistic links between Hes1 and Bmi-1/PTEN/Akt/GSK3β signaling in the development and progression of colon cancer.

Indexed as

Basic Helix-Loop-Helix ProteinsCell MovementCell ProliferationColonic NeoplasmsEpithelial-Mesenchymal TransitionGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHomeodomain ProteinsHumansNeoplasm InvasivenessNeoplasm MetastasisPolycomb Repressive Complex 1Proto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionTranscription Factor HES-1Basic Helix-Loop-Helix ProteinsBMI1 protein, humanGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGSK3B protein, humanHES1 protein, humanHomeodomain ProteinsPolycomb Repressive Complex 1Proto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanTranscription Factor HES-1Bmi-1colon cancerHes1metastasisPTEN

Identifiers

PMID26452029
PMCPMC4770728
OpenAlexW2176365353

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.