دورية أكاديمية

Tamoxifen induces eryptosis through calcium accumulation and oxidative stress.

التفاصيل البيبلوغرافية
العنوان: Tamoxifen induces eryptosis through calcium accumulation and oxidative stress.
المؤلفون: Alfhili MA; Chair of Medical and Molecular Genetics Research, Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, 12372, Riyadh, Saudi Arabia. malfeehily@ksu.edu.sa., Alyousef AM; Chair of Medical and Molecular Genetics Research, Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, 12372, Riyadh, Saudi Arabia., Alsughayyir J; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, 12372, Riyadh, Saudi Arabia.
المصدر: Medical oncology (Northwood, London, England) [Med Oncol] 2023 Oct 17; Vol. 40 (11), pp. 333. Date of Electronic Publication: 2023 Oct 17.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Springer Country of Publication: United States NLM ID: 9435512 Publication Model: Electronic Cited Medium: Internet ISSN: 1559-131X (Electronic) Linking ISSN: 13570560 NLM ISO Abbreviation: Med Oncol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2011- : New York : Springer
Original Publication: Northwood, Middlesex, England : Science and Technology Letters, c1994-
مواضيع طبية MeSH: Tamoxifen*/adverse effects , Eryptosis*, Humans ; Calcium/metabolism ; Fluorescein-5-isothiocyanate/metabolism ; Fluorescein-5-isothiocyanate/pharmacology ; Oxidative Stress ; Erythrocytes ; Hemolysis ; Ascorbic Acid/pharmacology ; Ascorbic Acid/metabolism ; Urea/metabolism ; Urea/pharmacology ; Reactive Oxygen Species/metabolism
مستخلص: Chemotherapy-related anemia is a major obstacle in anticancer therapy. Tamoxifen (TAM) is an antiestrogen prescribed for breast cancer patients with hemolytic potential and apoptotic properties in nucleated cells. However, the eryptotic activity of TAM has hitherto escaped the efforts of investigators. RBCs from apparently healthy volunteers were treated with 1-50 μM of TAM for 24 h at 37 °C. Hemoglobin leakage and LDH, AST, and AChE activities were photometrically determined while K + , Na + , and Mg 2+ were detected by ion-selective electrode. Flow cytometry was used to identify eryptotic cells by annexin-V-FITC, intracellular Ca 2+ by Fluo4/AM, sell size and morphology by FSC and SSC signals, respectively, and oxidative stress by H 2 DCFDA. Whole blood was also exposed to 30 μM of TAM for 24 h at 37 °C to examine the toxicity of TAM to WBCs and platelets. TAM caused Ca 2+ -independent, dose-responsive hemolysis accompanied by K + , LDH, and AST leakage without improving the mechanical stability of RBCs in hypotonic environments. TAM treatment also increased the proportion of cells positive for annexin-V-FITC, Fluo4, and DCF, along with diminished FSC and SSC signals and AChE activity. Notably, TAM toxicity was aggravated by sucrose but abrogated by vitamin C, PEG 8000, and urea. Moreover, TAM exhibited distinct cytotoxic profiles against leukocytes and platelets. TAM-induced eryptosis is characterized by breakdown of membrane asymmetry, inhibition of AChE activity, Ca 2+ accumulation, cell shrinkage, and oxidative stress. Vitamin C, PEG 8000, and urea may hold promise to subvert the undesirable toxic effects of TAM on RBCs.
(© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
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معلومات مُعتمدة: IFKSURC-1-4407 Deputyship for Research and Innovation, Ministry of Education, Saudi Arabia
فهرسة مساهمة: Keywords: Breast cancer; Eryptosis; Hemolysis; Tamoxifen
المشرفين على المادة: 094ZI81Y45 (Tamoxifen)
Q662QK8M3B (polyethylene glycol 8000)
SY7Q814VUP (Calcium)
I223NX31W9 (Fluorescein-5-isothiocyanate)
PQ6CK8PD0R (Ascorbic Acid)
8W8T17847W (Urea)
0 (Reactive Oxygen Species)
تواريخ الأحداث: Date Created: 20231017 Date Completed: 20231023 Latest Revision: 20231027
رمز التحديث: 20231027
DOI: 10.1007/s12032-023-02205-4
PMID: 37848569
قاعدة البيانات: MEDLINE
الوصف
تدمد:1559-131X
DOI:10.1007/s12032-023-02205-4