Evidence map›Paper›PMID 39046662›Full record

ArticleJournal of gastrointestinal cancer2024

The Prediction of DLL4 as a Prognostic Biomarker in Patients with Gastric Cancer Using Anti-DLL4 Nanobody.

Reza Afzalipour, Tannaz Abbasi-Dokht, Maryam Sheikh, Maryam Mohammadlou, Fatemeh Nili, Rasoul Baharlou

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Article in Journal of gastrointestinal cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Reza Afzalipour *Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Tannaz Abbasi-Dokht *Cancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Maryam SheikhCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Maryam MohammadlouCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Fatemeh NiliDepartment of Pathology, Cancer Institute, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Rasoul BaharlouCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran. baharlour@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiogenesis and cancer metastasis depend on the DLL4/Notch signaling pathway. A new approach to treating angiogenesis could inhibit or block this pathway. In the present study, we investigated DLL4 expression as a biomarker capable of predicting survival outcomes in gastric cancer patients using a novel anti-DLL4 Nanobody. PATIENTS AND

methodsBy using a recently developed anti-DLL4 Nanobody, the expression of DLL4 was evaluated in tissue samples from 135 gastric cancer patients. It was evaluated whether DLL4 expression is related to clinicopathological factors, overall survival (OS), and recurrence-free survival (RFS).

resultsSixty-five (48%) gastric cancer patients had a positive expression of DLL4 within the tumor tissue. Based on both the univariate and multivariate regression analyses, the expression of DLL4 was strongly associated with RFS (HR, 1.94; p = 0.008) and OS (HR, 2.06; p = 0.004). Moreover, the survival analysis demonstrated that DLL4 expression was a significant independent factor of unfavorable OS (HR, 2.7; p = 0.01) and RFS (HR, 2.3; p = 0.02) in gastric cancer patients.

conclusionDLL4 expression in gastric cancer patients may predict poor prognosis and survival. Furthermore, the current data demonstrate the potential of Nanobody for detecting DLL4, and it may lead to develop novel therapies and diagnostics for tumors.

Indexed as

Adaptor Proteins, Signal TransducingBiomarkers, TumorCalcium-Binding ProteinsStomach NeoplasmsAdultAgedAged, 80 and overFemaleHumansIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsMiddle AgedPrognosisSingle-Domain AntibodiesAdaptor Proteins, Signal TransducingBiomarkers, TumorCalcium-Binding ProteinsDLL4 protein, humanIntracellular Signaling Peptides and ProteinsMembrane ProteinsSingle-Domain AntibodiesAnti-DLL4 NanobodyDLL4Gastric cancerImmunohistochemistryPrognosis

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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.