دورية أكاديمية

HOXA1 silencing inhibits cisplatin resistance of oral squamous cell carcinoma cells via IκB/NF-κB signaling pathway.

التفاصيل البيبلوغرافية
العنوان: HOXA1 silencing inhibits cisplatin resistance of oral squamous cell carcinoma cells via IκB/NF-κB signaling pathway.
المؤلفون: Zhu R; School of Stomatology, Xuzhou Medical University., Mao Y; School of Stomatology, Xuzhou Medical University., Xu X; School of Stomatology, Xuzhou Medical University., Li Y; School of Stomatology, Xuzhou Medical University., Zheng J; School of Stomatology, Xuzhou Medical University.; Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
المصدر: Anti-cancer drugs [Anticancer Drugs] 2024 Jul 01; Vol. 35 (6), pp. 492-500. Date of Electronic Publication: 2024 Mar 12.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9100823 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5741 (Electronic) Linking ISSN: 09594973 NLM ISO Abbreviation: Anticancer Drugs Subsets: MEDLINE
أسماء مطبوعة: Publication: London : Lippincott Williams & Wilkins
Original Publication: Oxford, UK : Rapid Communications of Oxford, [1990-
مواضيع طبية MeSH: Cisplatin*/pharmacology , Mouth Neoplasms*/drug therapy , Mouth Neoplasms*/pathology , Mouth Neoplasms*/genetics , Drug Resistance, Neoplasm* , Homeodomain Proteins*/genetics , Homeodomain Proteins*/metabolism , Signal Transduction*/drug effects , NF-kappa B*/metabolism, Humans ; Apoptosis/drug effects ; Carcinoma, Squamous Cell/drug therapy ; Carcinoma, Squamous Cell/genetics ; Carcinoma, Squamous Cell/pathology ; Carcinoma, Squamous Cell/metabolism ; Antineoplastic Agents/pharmacology ; Cell Line, Tumor ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Squamous Cell Carcinoma of Head and Neck/drug therapy ; Squamous Cell Carcinoma of Head and Neck/genetics ; Squamous Cell Carcinoma of Head and Neck/pathology ; Squamous Cell Carcinoma of Head and Neck/metabolism ; NF-KappaB Inhibitor alpha/metabolism ; Cell Survival/drug effects ; Cell Proliferation/drug effects ; I-kappa B Proteins/metabolism
مستخلص: The resistance of oral squamous cell carcinoma (OSCC) cells to cisplatin remains a tough nut to crack in OSCC therapy. Homeobox A1 (HOXA1) overexpression has been detected in head and neck squamous carcinoma (HNSC). Accordingly, this study aims to explore the potential role and mechanism of HOXA1 on cisplatin resistance in OSCC. The expression of HOXA1 in HNSC and its role in overall survival (OS) rate of OSCC patients were analyzed by bioinformatic analysis. Following transfection as needed, OSCC cells were induced by different concentrations of cisplatin, and the cell viability and apoptosis were evaluated by cell counting kit-8 and flow cytometry assays. The mRNA and protein expression levels of HOXA1 and the phosphorylation of IκBα and p65 were determined by real-time quantitative PCR and western blot. HOXA1 expression level was upregulated in HNSC tissues and OSCC cells. Overexpressed HOXA1 was correlated with a low OS rate of OSCC patients. Cisplatin exerted an anti-cancer effect on OSCC cells. HOXA1 silencing or cisplatin suppressed OSCC cell viability, boosted the apoptosis, and repressed the phosphorylation of IκBα and p65. Intriguingly, the combination of HOXA1 silencing and cisplatin generated a stronger anti-cancer effect on OSCC cells than their single use. HOXA1 silencing attenuates cisplatin resistance of OSCC cells via IκB/NF-κB signaling pathway, hinting that HOXA1 is a biomarker associated with OSCC and HOXA1 silencing can enhance the sensitivity of OSCC cells to cisplatin.
(Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.)
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المشرفين على المادة: Q20Q21Q62J (Cisplatin)
0 (Homeodomain Proteins)
0 (homeobox A1 protein)
0 (NF-kappa B)
0 (Antineoplastic Agents)
0 (Transcription Factors)
139874-52-5 (NF-KappaB Inhibitor alpha)
0 (I-kappa B Proteins)
تواريخ الأحداث: Date Created: 20240313 Date Completed: 20240508 Latest Revision: 20240512
رمز التحديث: 20240513
DOI: 10.1097/CAD.0000000000001592
PMID: 38477942
قاعدة البيانات: MEDLINE
الوصف
تدمد:1473-5741
DOI:10.1097/CAD.0000000000001592