دورية أكاديمية
Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer.
العنوان: | Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer. |
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المؤلفون: | Elsayad KA; Pharmacy Department, Cairo University Hospitals, Cairo University, Cairo, 11662, Egypt; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, 11562, Cairo, Egypt. Electronic address: khaled.al.elsayad@std.pharma.cu.edu.eg., Elmasry GF; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, 11562, Cairo, Egypt. Electronic address: ghada.elmasry@pharma.cu.edu.eg., Mahmoud ST; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, 11562, Cairo, Egypt., Awadallah FM; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, 11562, Cairo, Egypt. |
المصدر: | Bioorganic chemistry [Bioorg Chem] 2024 Jun; Vol. 147, pp. 107409. Date of Electronic Publication: 2024 Apr 29. |
نوع المنشور: | Journal Article; Review |
اللغة: | English |
بيانات الدورية: | Publisher: Elsevier Country of Publication: United States NLM ID: 1303703 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1090-2120 (Electronic) Linking ISSN: 00452068 NLM ISO Abbreviation: Bioorg Chem Subsets: MEDLINE |
أسماء مطبوعة: | Publication: Amsterdam : Elsevier Original Publication: New York, London, Academic Press. |
مواضيع طبية MeSH: | Sulfonamides*/chemistry , Sulfonamides*/pharmacology , Sulfonamides*/chemical synthesis , Antineoplastic Agents*/pharmacology , Antineoplastic Agents*/chemistry , Antineoplastic Agents*/chemical synthesis , Neoplasms*/drug therapy , Neoplasms*/pathology , Neoplasms*/metabolism, Humans ; Molecular Structure ; Cell Proliferation/drug effects ; Animals ; Structure-Activity Relationship |
مستخلص: | Sulfonamides have gained prominence as versatile agents in cancer therapy, effectively targeting a spectrum of cancer-associated enzymes. This review provides an extensive exploration of their multifaceted roles in cancer biology. Sulfonamides exhibit adaptability by acting as tyrosine kinase inhibitors, disrupting pivotal signaling pathways in cancer progression. Moreover, they disrupt pH regulation mechanisms in cancer cells as carbonic anhydrase inhibitors, inhibiting growth, and survival. Sulfonamides also serve as aromatase inhibitors, interfering with estrogen synthesis in hormone-driven cancers. Inhibition of matrix metalloproteinases presents an opportunity to impede cancer cell invasion and metastasis. Additionally, their emerging role as histone deacetylase inhibitors offers promising prospects in epigenetic-based cancer therapies. These diverse roles underscore sulfonamides as invaluable tools for innovative anti-cancer treatments, warranting further exploration for enhanced clinical applications and patient outcomes. Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. (Copyright © 2024 Elsevier Inc. All rights reserved.) |
التعليقات: | Erratum in: Bioorg Chem. 2024 Jul 1:107583. doi: 10.1016/j.bioorg.2024.107583. (PMID: 38955547) |
فهرسة مساهمة: | Keywords: Aromatase; Cancer; Carbonic anhydrase; Histone deacetylase; Matrix metalloproteinases; Sulfonamides; Tyrosine kinases |
تواريخ الأحداث: | Date Created: 20240507 Date Completed: 20240516 Latest Revision: 20240702 |
رمز التحديث: | 20240703 |
DOI: | 10.1016/j.bioorg.2024.107409 |
PMID: | 38714116 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1090-2120 |
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DOI: | 10.1016/j.bioorg.2024.107409 |