Evidence map›Paper›PMID 39687450›Full record

ArticleIranian journal of pathology2024

Regulation of Tumor Vascular Microenvironment by Nestin and Fms-related Tyrosine Kinase 1 (FLT1) and Their Prognostic Significance in Renal Cell Carcinoma.

Noha Elkady, Reham Ahmed Abdelaziz, Rasha Adel Abdelmoneum, Ahmed S Ghonaimy, Dina Mohamed Allam

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Article in Iranian journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Noha ElkadyDepartment of Pathology, Faculty of Medicine, Menoufia University, Shibin Elkom, Egypt.
Reham Ahmed AbdelazizDepartment of Clinical Oncology and Nuclear MedicineFaculty of Medicine, Menoufia University, Egypt.
Rasha Adel AbdelmoneumDepartment of Clinical Oncology and Nuclear MedicineFaculty of Medicine, Menoufia University, Egypt.
Ahmed S GhonaimyDepartment of Urology, Faculty of Medicine, Menoufia University, Shibin Elkom, Egypt.
Dina Mohamed AllamDepartment of Pathology, Faculty of Medicine, Menoufia University, Shibin Elkom, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Objective: Hypervascularity is a characteristic feature of renal cell carcinoma (RCC) and microvessel density (MVD) predicts tumor metastasis. Nestin is a stem cell marker that is expressed in proliferating endothelial cells and newly formed vessels and Fms-related tyrosine kinase 1 (FLT1) is a proangiogenic factor. This study aimed to evaluate the expression of Nestin and FLT1 in RCC and their prognostic impact. Methods: This retrospective study included sixty cases of RCC after obtaining ethical approval. Sections were immunohistochemically stained by Nestin and FLT1 then their expressions were compared to different clinicopathological parameters. MVD was evaluated using Nestin and CD34 and compared to the different parameters. Results: Nestin was expressed mainly in endothelial cells of small vessels in 65% of cases while FLT1 was expressed in tumor and endothelial cells in 73.3% of cases. Their expressions were significantly associated with aggressive tumor parameters including larger tumors, high-grade tumors, wider tumor extension, and advanced stage. Moreover, Nestin expression was significantly associated with metastasis. MVD evaluated by Nestin showed more associations with larger tumors, high-grade tumors, wider tumor extension, advanced stage, and metastasis than MVD measured by CD34. Nestin and FLT1 positivity and high MVD measured by Nestin were significantly associated with short overall survival. Conclusion: Nestin and FLT1 expressions in RCC may be associated with aggressive tumor features and short patients' overall survival. MVD evaluated by Nestin may be correlated with tumor progression and metastasis. Nestin and FLT1 may be used as prognostic biomarkers in RCC.

Indexed as

FLT1MVDNestinPrognosisRCC

Identifiers

PMID39687450
PMCPMC11646198

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