Evidence map›Paper›PMID 38522060›Full record

ArticleMedical molecular morphology2024

P4HA2 involved in SLUG-associated EMT predicts poor prognosis of patients with KRAS-positive colorectal cancer.

Heba El-Deek Mohammed El-Deek, Maha Salah El-Naggar, Aiat Morsy Mohamed Morsy, Mayada Fawzy Sedik, Heba Ahmed Osman, Asmaa M Ahmed

Open access · hybridAbstract read
In one paragraph

Article in Medical molecular morphology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Review
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 2 institutions in 1 country.

Heba El-Deek Mohammed El-DeekDepartment of Pathology, Faculty of Medicine, Assiut University, Assiut, Egypt. Hebaeldeek@gmail.com.ORCID http://orcid.org/0000-0001-8963-2044
Maha Salah El-NaggarDepartment of Clinical Oncology, Faculty of Medicine, Assiut University Hospital, Assiut, Egypt.
Aiat Morsy Mohamed MorsyDepartment of Clinical Oncology, Faculty of Medicine, Assiut University Hospital, Assiut, Egypt.
Mayada Fawzy SedikDepartment of Medical Oncology and Hematological Malignancies, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.
Heba Ahmed OsmanDepartment of Tropical Medicine and Gastroenterology, Faculty of Medicine, South Valley University, Qena, Egypt.
Asmaa M AhmedDepartment of Pathology, Faculty of Medicine, Assiut University, Assiut, Egypt.
Assiut University · EGSouth Valley University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to examine the immunohistochemical expression of epithelial-mesenchymal transition biomarkers: P4HA2 and SLUG in colorectal carcinoma (CRC) specimens, then to assess their relation to clinicopathological features including KRAS mutations and patients' survival, and finally to study the correlation between them in CRC. The result of this study showed that SLUG and P4HA2 were significantly higher in association with adverse prognostic factors: presence of lympho-vascular invasion, perineural invasion, higher tumor budding, tumor stage, presence of lymph node metastasis, and presence of distant metastasis. CRC specimens with KRAS mutation were associated with significant higher SLUG and P4HA2 expression. High expression of both SLUG and P4HA2 was significantly unfavorable prognostic indicator as regards overall survival (OS) and disease-free survival (DFS). In KRAS mutated cases, high P4HA2 expression was the only significant poor prognostic indicator as regarding DFS. In conclusions, our data highlight that both SLUG and P4HA2 expression may serve as potentially important poor prognostic biomarkers in CRC and targeting these molecules may be providing a novel therapeutic strategy. In KRAS mutation group, high P4HA2 expression is the only independent prognostic factor for tumor recurrence, so it can be suggested to be a novel target for therapy.

Indexed as

Biomarkers, TumorColorectal NeoplasmsEpithelial-Mesenchymal TransitionMutationProto-Oncogene Proteins p21(ras)Snail Family Transcription FactorsAdultAgedDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisProlyl HydroxylasesBiomarkers, TumorKRAS protein, humanP4HA2 protein, humanProlyl HydroxylasesProto-Oncogene Proteins p21(ras)SNAI1 protein, humanSNAI2 protein, humanSnail Family Transcription FactorsCRCP4HA2SLUG

Identifiers

PMID38522060
PMCPMC11343967
OpenAlexW4393122345

What OpenQuestion holds

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LicenceCC BY
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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.