4.7 Article

The Role of Cell Proliferation and Extracellular Matrix Accumulation Induced by Food Additive Butylated Hydroxytoluene in Uterine Leiomyoma

期刊

NUTRIENTS
卷 13, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/nu13093074

关键词

butylated hydroxytoluene; leiomyoma; uterine fibroids; extracellular matrix; matrix metalloproteinase; environmental exposure

资金

  1. Ministry of Science and Technology, Taiwan [MOST 110-2628-B-038-018, MOST 109-2314-B038-059, MOST 109-2628-B-038-015, MOST 109-2320-B-254-001, MOST 109-2811-B-038-523]
  2. Ministry of Education, Taiwan [MOE-RSC-108RSN0005]

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BHT, a synthetic phenolic antioxidant commonly used in food and cosmetics, has been found to potentially promote the progression of leiomyoma by increasing extracellular matrix production and matrix metalloproteinase expression. This effect may be mediated through the activation of the PI3K/Akt and MAPK signaling pathways.
Leiomyoma is the most common benign uterine tumor in reproductive-age women. Increasing numbers of studies are focusing on the effects of environmental exposure on the incidence and progression of tumors. One major step taken in the food industry is the addition of food preservatives to maintain freshness. Butylated hydroxytoluene (BHT) is a synthetic phenolic antioxidant, which is widely used as an additive to develop fat-soluble characteristics, as well as in cosmetics and rubber. Previous studies also highlighted that BHT may be related to increased fibrosis capacity and carcinogenic effects. In this study, we explored the effects of the commonly used food additive BHT on leiomyoma progression, and the related mechanism. The exposure of the ELT-3 leiomyoma cell line to BHT for 48 h increased the proliferative effect. Since leiomyoma progression is related to increases in extracellular matrix (ECM) accumulation and matrix metalloproteinase (MMP), BHT could effectively increase ECM-related protein expression, as well as MMP-2 and MMP-9 protein expression. This increase in ECM, in response to BHT, may be linked to the activation of the phosphoinositide 3-kinase (PI3K)/Akt and mitogen-activated protein kinase (MAPK) signaling pathway. Through PI3K inhibition, BHT's effect on leiomyoma progression could be partially modulated. These results suggest the harmful effect of BHT exposure on leiomyoma progression may relate to PI3K modulation. However, an in vivo study is necessary to confirm these findings.

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