Evidence map›Paper›PMID 25206290›Full record

ArticleWorld journal of gastroenterology2014

Identification of differential proteins in colorectal cancer cells treated with caffeic acid phenethyl ester.

Yu-Jun He, Wan-Ling Li, Bao-Hua Liu, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Yu-Jun HeYu-Jun He, Wan-Ling Li, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu, Institute of Immunology of PLA, the Third Military Medical University, Chongqing 400038, China.
Wan-Ling LiYu-Jun He, Wan-Ling Li, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu, Institute of Immunology of PLA, the Third Military Medical University, Chongqing 400038, China.
Bao-Hua LiuYu-Jun He, Wan-Ling Li, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu, Institute of Immunology of PLA, the Third Military Medical University, Chongqing 400038, China.
Hui DongYu-Jun He, Wan-Ling Li, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu, Institute of Immunology of PLA, the Third Military Medical University, Chongqing 400038, China.
Zhi-Rong MouYu-Jun He, Wan-Ling Li, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu, Institute of Immunology of PLA, the Third Military Medical University, Chongqing 400038, China.
Yu-Zhang WuYu-Jun He, Wan-Ling Li, Hui Dong, Zhi-Rong Mou, Yu-Zhang Wu, Institute of Immunology of PLA, the Third Military Medical University, Chongqing 400038, China.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the molecular mechanisms of the anti-cancer activity of caffeic acid phenethyl ester (CAPE).

methodsProtein profiles of human colorectal cancer SW480 cells treated with or without CAPE were analysed using a two-dimensional (2D) electrophoresis gel-based proteomics approach. After electrophoresis, the gels were stained with Coomassie brilliant blue R-250. Digital images were taken with a GS-800 Calibrated Densitometer, and image analysis was performed using PDQuest 2-D Analysis software. The altered proteins following CAPE treatment were further identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry following a database search. The identified proteins were validated by Western blot and immunofluorescence assay.

resultsCAPE induced human colorectal cancer cell apoptosis. Four up-regulated proteins and seven down-regulated proteins in colorectal cancer cells treated with CAPE were found. The identified down-regulated proteins in CAPE-treated colorectal cancer cells were Triosephosphate Isomerase (Tim), Proteasome subunit alpha 4 (PSMA4) protein, Guanine nucleotide binding protein beta, Phosphoserine aminotransferase 1 (PSAT1), PSMA1, Myosin XVIIIB and Tryptophanyl-tRNA synthetase. Notably, CAPE treatment led to the down-regulation of PSAT1 and PSMA1, two proteins that have been implicated in tumorigenesis. The identified up-regulated proteins were Annexin A4, glyceraldehyde-3-phosphate dehydrogenase, Glucosamine-6-phosphate deaminase 1 (GNPDA1), and Glutathione peroxidase (GPX-1). Based on high match scores and potential role in cell growth control, PSMA1, PSAT1, GNPDA1 and GPX-1 were further validated by Western blotting and immunofluorescence assay. PSMA1 and PSAT1 were down-regulated, while GNPDA1 and GPX-1 were up-regulated in CAPE-treated colorectal cancer cells.

conclusionThese differentiated proteins in colorectal cancer cells following CAPE treatment, may be potential molecular targets of CAPE and involved in the anti-cancer effect of CAPE.

Indexed as

ProteomicsAntineoplastic AgentsApoptosisBiomarkers, TumorBlotting, WesternCaffeic AcidsCell Line, TumorCell ProliferationColorectal NeoplasmsElectrophoresis, Gel, Two-DimensionalFluorescent Antibody TechniqueHumansMicroscopy, ConfocalNeoplasm ProteinsPhenylethyl AlcoholReproducibility of ResultsAntineoplastic AgentsBiomarkers, Tumorcaffeic acid phenethyl esterCaffeic AcidsNeoplasm ProteinsPhenylethyl AlcoholCaffeic acid phenethyl esterColorectal cancerMass spectrometryProteomicsTwo-dimensional electrophoresis

Identifiers

PMID25206290
PMCPMC4155376
OpenAlexW1988986339

What OpenQuestion holds

Textmetadata
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.