Article Publish Status: FREE
Abstract Title:

Epigallocatechin-3-gallate inhibits doxorubicin-induced inflammation on human ovarian tissue.

Abstract Source:

Biosci Rep. 2019 Apr 17. Epub 2019 Apr 17. PMID: 30996116

Abstract Author(s):

Raffaella Fabbri, Maria Macciocca, Rossella Vicenti, Giacomo Caprara, Marie-Pierre Piccinni, Roberto Paradisi, Patrizia Terzano, Alessio Papi, Renato Seracchioli

Article Affiliation:

Raffaella Fabbri


Chemotherapy protocol can destroy the reproductive potential of young cancer patients. Doxorubicin (DOX) is a potent anthracycline commonly used in the treatment of numerous malignancies. The purpose of the study was to evaluate the ovarian toxicity of DOX via inflammation and the possible protective effect of the green tea polyphenol epigallocatechin-3-gallate (EGCG). Ovarian tissue of three patients was cultured with 1µg/ml DOX and/or 10µg/ml EGCG for 24 and 48 hours. Levels of inflammatory factors were determined by western blot, zimography, quantitative Real-Time PCR and multiplex bead-based immunoassay. Morphological evaluation, damaged follicle count and TUNEL assay were also performed. DOX influenced inflammatory responses by inducing a significant increase in the expression of pro-inflammatory cytokines, such as tumor necrosis factor-α (TNF-α) and cyclooxigenase-2 (COX-2), of inflammatory interleukins, such as interleukin-6 (IL-6) and interleukin-8 (IL-8), and the inflammatory proteins mediators metalloproteinase-2 and metalloproteinase-9 (MMP2 and MMP9). IL-8 secretion in the culture supernatants and MMP9 activity also significantly raised after DOX treatment. Moreover, a histological evaluation of the ovarian tissue showed morphological damage to follicles and stroma after DOX exposure. EGCG significantly reduced DOX-induced inflammatory responses and improved the preservation of follicles.: DOX-induced inflammation could be responsible for the ovarian function impairment of chemotherapy. EGCG could have a protective role in reducing DOX-mediated inflammatory responses in human ovarian tissue.

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