Evidence map›Paper›PMID 41141138›Full record

ArticleCureus2025

Intertwined Relationship of WWOX and RUNX2 Proteins as a Biomarker for Predicting Response and Survival in Patients With Childhood Bone Cancer in North India: A Pilot Study.

Priyanka Sharma, Shah Waliullah, Bhavesh Kumar, Ravindra Mohan, Devarshi Rastogi, Dharmendra Kumar, Wahid Ali

Abstract read
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Article in Cureus, 2025. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Priyanka SharmaPathology, King George's Medical University, Lucknow, IND.
Shah WaliullahOrthopaedic Surgery, King George's Medical University, Lucknow, IND.
Bhavesh KumarOrthopaedic Surgery, King George's Medical University, Lucknow, IND.
Ravindra MohanOrthopaedic Surgery, King George's Medical University, Lucknow, IND.
Devarshi RastogiOrthopaedic Surgery, King George's Medical University, Lucknow, IND.
Dharmendra KumarOrthopaedic Surgery, King George's Medical University, Lucknow, IND.
Wahid AliPathology, King George's Medical University, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEwing sarcoma (ES) is an aggressive bone cancer that predominantly affects children and adolescents. Despite advancements in treatment, the prognosis for patients with metastatic disease remains poor. This pilot study investigated the expression of WWOX and RUNX2 proteins in ES tissues from patients from North India and their potential as prognostic biomarkers.

methodsImmunohistochemical analysis was performed on tumor samples from seven ES patients and five age-matched controls.

resultsThe results revealed that RUNX2 expression was significantly elevated in ES tissues compared to controls (p = 0.005), while WWOX expression showed no significant difference (p = 0.876). Clinically, 71.4% of patients presented with stage IV disease, and 85.7% had metastasis at diagnosis. The Kaplan-Meier analysis demonstrated poor survival outcomes, with a high mortality rate (85.7%) and reduced median survival time.

conclusionThese findings suggest that RUNX2 overexpression is a defining characteristic of ES and may contribute to tumor progression and metastasis. In contrast, WWOX does not appear to play a critical role in ES pathogenesis. The advanced stage at presentation and poor survival outcomes underscore the need for earlier detection and biomarker-driven interventions. Further research is warranted to validate RUNX2 as a prognostic biomarker and potential therapeutic target in ES.

Indexed as

ewing sarcomanorth indian populationprognosisrunx2wwox

Identifiers

PMID41141138
PMCPMC12552799

What Socratic holds

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LicenceCC BY
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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 Socratic graph.