Evidence map›Paper›PMID 39523086›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2024

[Colorectal fibroblasts promote malignant phenotype of colorectal cancer cells by activating the ERK signaling pathway].

X Xi, T Deng, B DU

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

X XiDepartment of Immunology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
T DengDepartment of Immunology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.
B DUDepartment of Immunology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of human colorectal fibroblast (CCD-18Co)-conditioned medium (CCD18-Co-CM) on biological behaviors of colorectal cancer (CRC) cells and explore the possible molecular mechanisms.

methodsReal-time cellular analysis (RTCA), clone formation assay and wound healing assay were used to analyze the changes in proliferation, clone formation, and migration abilities of CRC cell lines HCT116 and Caco-2 treated with CCD18-Co-CM. Western blotting was used to detect the changes in ATK, ERK and STAT3 signaling pathways in the CRC cells activated by CCD18-Co-CM. The effect of CCD18-Co-CM on spheroidization ability of the cells was assessed with sphere-formation assay, and the changes in expressions of CRC stemness markers were detected using RT-PCR.

resultsCCD-18Co-CM significantly promoted proliferation, colony formation, and migration of HCT116 and Caco-2 cells, enhanced sphere-forming ability and expressions of CRC stemness markers, and increased ERK phosphorylation in the cells. Treatment with SCH772984 effectively inhibited CCD-18Co-CM-induced ERK signaling pathway activation, suppressed the malignant phenotype, and lowered the sphere-forming ability and expression of stemness markers of the two CRC cells.

conclusionColorectal fibroblasts promote malignant phenotype of CRC cells by activating the ERK signaling pathway.

Indexed as

Cell MovementCell ProliferationColorectal NeoplasmsFibroblastsMAP Kinase Signaling SystemCaco-2 CellsCell Line, TumorCulture Media, ConditionedHCT116 CellsHumansIndazolesPhenotypePhosphorylationPiperazinesSTAT3 Transcription FactorCulture Media, ConditionedIndazolesPiperazinesSCH772984STAT3 protein, humanSTAT3 Transcription Factorcolorectal cancerERKfibroblastsstemness

Identifiers

PMID39523086
PMCPMC11526459

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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.