Evidence map›Paper›PMID 35292013›Full record

ArticleCancer cell international2022

NCAPG facilitates colorectal cancer cell proliferation, migration, invasion and epithelial-mesenchymal transition by activating the Wnt/β-catenin signaling pathway.

Yanlong Shi, Chang Ge, Debao Fang, Wei Wei, Li Li, Qian Wei, Hongzhu Yu

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
5.7field-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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  11. Wnt/β-catenin-driven EMT regulation in human cancers.Cellular and molecular life sciences : CMLS · 2024
    Review
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  16. Cancer spreading patterns based on epithelial-mesenchymal plasticity.Frontiers in cell and developmental biology · 2024
    Article
  17. Article
  18. Animals : an open access journal from MDPI · 2023
    Article
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Yanlong ShiDepartment of General Surgery, Fuyang Hospital Affiliated to Anhui Medical University, Fuyang, 236000, Anhui, China.
Chang GeDepartment of General Surgery, Fuyang Hospital Affiliated to Anhui Medical University, Fuyang, 236000, Anhui, China.
Debao FangSchool of Life Sciences and Medical Center, University of Science & Technology of China, Hefei, 230000, Anhui, China.
Wei WeiDepartment of General Surgery, Fuyang Hospital Affiliated to Anhui Medical University, Fuyang, 236000, Anhui, China.
Li LiDepartment of General Surgery, Fuyang Hospital Affiliated to Anhui Medical University, Fuyang, 236000, Anhui, China.
Qian WeiSchool of Nursing, Anhui Medical University, HeFei, 230000, Anhui, China.
Hongzhu YuDepartment of General Surgery, Fuyang Hospital Affiliated to Anhui Medical University, Fuyang, 236000, Anhui, China. hongzhuyu@ahmu.edu.cn.ORCID http://orcid.org/0000-0002-6533-7718
Anhui Medical University · CNUniversity of Science and Technology of China · CN

Funding

the Health Commission of Anhui Province AHWJ2021b138
6 · The paper itself

Abstract

backgroundThe condensation complex gene non-SMC condensin I complex subunit G(NCAPG), a cell cycle-associated condensin, is over-expressed in various cancers. However, its biological function in colorectal cancer (CRC) has yet to be deciphered. In this study, we investigated the role of NCAPG in CRC progression.

methodsTissues and cells were used to measure NCAPG expression levels and their association with clinicopathological characteristics. NCAPG silencing and overexpression in CRC cells were used to measure its effect on proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT) progression. In addition, mRNA, and protein expression levels of key EMT biomarkers were measured. The underlying mechanism of NCAPG modulating CRC progression was further explored using western blotting, co-immunoprecipitation (CO-IP), and immunofluorescence (IF) assays.

resultsNCAPG was over-expressed in CRC tissues and cell lines. High expression levels were associated with differentiation levels, lymph metastasis, and vascular invasion in patients. NCAPG silencing suppressed, while NCAPG overexpression promoted the proliferative, migration, and invasive capacity of HCT116 and SW480 cells. Mechanistically, we discovered that NCAPG participated in regulating the EMT process and the Wnt/β-catenin signaling pathway to facilitate CRC invasion and metastasis. Additional experiments demonstrated that NCAPG activated the Wnt/β-catenin signaling pathway by binding to β-catenin in CRC cells.

conclusionNCAPG acts as an oncogene involved in the development and progression of CRC by binding to β-catenin to activate the Wnt/β-catenin signaling pathway.

Indexed as

Colorectal cancerEpithelial–mesenchymal transitionNCAPGWnt/β-catenin signaling pathway

Identifiers

PMID35292013
PMCPMC8922890
OpenAlexW4220858799

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.