Evidence map›Paper›PMID 29681001›Full record

ArticleJournal of gastrointestinal cancer2019

Immunohistochemical Expression of Fatty Acid Synthase and Vascular Endothelial Growth Factor in Primary Colorectal Cancer: a Clinicopathological Study.

Asmaa Hussein Mohamed, Nelly Mohamed Said

Abstract read
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Article in Journal of gastrointestinal cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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  8. DysregulatedReports of biochemistry & molecular biology · 2019
    Article
  9. CD147 promotes cervical cancer migration and invasion by up-regulating fatty acid synthase expression.International journal of clinical and experimental pathology · 2019
    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

2 authors at 1 institution in 1 country.

Asmaa Hussein MohamedDepartment of Pathology, Faculty of Medicine, Zagazig University, Ash Sharqia Governorate, Zagazig, 44519, Egypt. drasmaahussein@yahoo.com.
Nelly Mohamed SaidDepartment of Pathology, Faculty of Medicine, Zagazig University, Ash Sharqia Governorate, Zagazig, 44519, Egypt.
Zagazig University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFatty acid synthase (FAS) is a valuable lipid enzyme involved in lipid biosynthesis and suggested to contribute in tumor carcinogenesis. Vascular endothelial growth factor (VEGF) is considered a serious angiogenic growth factor in the angiogenic pathway which is a very important in tumor growth and metastasis. Thus, inhibition of lipid biosynthesis and tumor angiogenesis can be new goals for colorectal cancer (CRC) treatment. AIM OF THE WORK: The assessment of the expression of FAS and VEGF protein and the relationship between them in CRC with the clinicopathological parameters.

methodsThe present retrospective study included 63 paraffin blocks previously diagnosed as primary cases of CRC. The slides were subjected to FAS and VEGF immunohistochemical staining using a streptavidin-biotin-peroxidase. The relationships among FAS and VEGF expression and clinicopathological parameters were statistically analyzed.

resultsThe expression rate of FAS was 81% and VEGF was 84.1% in the studied cases. FAS expression was significantly associated with histopathological type (p = 0.02) and grade (p = 0.04), and highly associated with lymph node metastasis and stage (p < 0.001).VEGF was significantly associated with histopathological type (p = 0.01) and tumor depth (p = 0.02); highly associated with grade, lymph node metastasis, and stage (p < 0.001). There was a positive association between FAS and VEGF expression in CRC (p < 0.001).

conclusionFAS and VEGF showed a highly significant expression in the studied primary CRC cases. A significant association was observed between their expressions, suggesting the involvement of FAS in tumor angiogenesis. So they constitute potential targets in cancer prevention and treatment and make FAS an attractive antiangiogenic target.

Indexed as

AdenocarcinomaAdenocarcinoma, MucinousAdultAgedBiomarkers, TumorCarcinoma, Signet Ring CellCase-Control StudiesColorectal NeoplasmsFatty Acid Synthase, Type IFemaleFollow-Up StudiesHumansLymphatic MetastasisMaleMiddle AgedNeovascularization, PathologicBiomarkers, TumorFASN protein, humanFatty Acid Synthase, Type IVascular Endothelial Growth Factor AVEGFA protein, humanColorectal cancerFatty acid synthaseImmunohistochemical studyVascular endothelial growth factor

Identifiers

PMID29681001
OpenAlexW2801535883

What OpenQuestion holds

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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.