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Updated: Dec 13, 2025

A Syngeneic Orthotopic Osteosarcoma Sprague Dawley Rat Model with Amputation to Control Metastasis Rate
Published on: May 3, 2021
Suppression of adriamycin resistance in osteosarcoma by blocking Wnt/β-catenin signal pathway
1Department of Orthopedics, First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Abstract:
Since this article has been suspected of research misconduct and the corresponding authors did not respond to our request to prove originality of data and figures, "Suppression of adriamycin resistance in osteosarcoma by blocking Wnt/β-catenin signal pathway, by B.-Q. Wu, Y. Cao, Z.-G. Bi, published in Eur Rev Med Pharmacol Sci 2017; 21 (14): 3185-3192-PMID: 28770967" has been withdrawn. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/13139.
Insights
This article on adriamycin resistance in osteosarcoma has been withdrawn due to suspected research misconduct. The publisher retracted the study after authors failed to verify data originality.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Adriamycin resistance is a significant challenge in osteosarcoma treatment.
- The Wnt/β-catenin signaling pathway is implicated in various cancers, including osteosarcoma.
Purpose of the Study:
- To investigate the potential of blocking the Wnt/β-catenin signal pathway to suppress adriamycin resistance in osteosarcoma.
Main Methods:
- The study aimed to explore the molecular mechanisms underlying adriamycin resistance.
- Investigated the role of the Wnt/β-catenin pathway in modulating drug resistance.
Main Results:
- The article reported that suppressing the Wnt/β-catenin pathway could inhibit adriamycin resistance in osteosarcoma.
- Specific molecular targets and pathways were discussed in relation to this effect.
Conclusions:
- The findings suggested a potential therapeutic strategy for overcoming adriamycin resistance in osteosarcoma.
- Blocking the Wnt/β-catenin pathway was proposed as a method to enhance chemotherapy efficacy.
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