Regulation of angiogenesis and inflammatory pathways by glycyrrhizic acid

Author:

Mohamed Doaa D.1,Mahrous Hoda1,Khalil Hany2,Ibrahim Ibrahim A.3,Mohamed Dalia D.1,Keshk Omar S.45,Nada Alaa H.1,Maksoud Ahmed I. Abd El67

Affiliation:

1. Department of Industrial Biotechnology, Genetic Engineering and Biotechnology Research Institute, University of Sadat City, Sadat City, Egypt

2. Department of Molecular Biology, Genetic Engineering and Biotechnology Research Institute, University of Sadat City, Sadat City, Egypt

3. Plant Biotechnology Department, Genetic Engineering and Biotechnology Research Institute, University of Sadat City, Sadat City, Egypt

4. College of Biotechnology, Misr University for Science and Technology, 6th of October City, Egypt

5. Laboratory of Computational Systems Biotechnology (LCSB), École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland

6. Department of Industrial Biotechnology, Genetic Engineering and Biotechnology Research Institute (GEBRI), University of Sadat City, Sadat City, 32897, Egypt

7. Department of Pharmaceutical Biotechnology, College of Biotechnology, Misr University of Science and Technology, Giza, 3236101, Egypt

Abstract

Skin cancer accounts for most malignancies across the globe. They are primarily divided into melanoma and nonmelanoma skin malignancies. Nonmelanoma skin cancer includes basal cell carcinoma and squamous cell carcinoma. Glycyrrhetinic acid (GA) is a bioactive compound extracted from licorice that exhibits an inhibition effect on various cancers. GA has been reported to have in vitro cytotoxic effects on several human cancer cells. However, reports on the mode of action and detailed mechanism of GA in vitro in skin cancer disease are limited. Hence, GA’s effect on the human skin cell line BJ and MCC13 was investigated. MTT assay showed that GA had cytotoxic effects on MCC13 cells but was non-toxic to the normal cells of BJ in a time-dose dependent manner. GA also inhibited the angiogenic sprouting of new blood vessels in tumor progression. In gene expression assay, GA induces mitochondrial apoptosis through the induction and inhibition of Cytochrome C and Bcl2 respectively. In conclusion, GA is a potent candidate to induce apoptosis and concurrently inhibit the invasion, migration, and angiogenesis of the MCC13 cell line through increasing TNF-alpha concentration resulting in the necroptotic pathway induction.

Publisher

Medknow

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