Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1

In recent years, Bisphenol S (BPS) has increasingly been used as an alternative to Bisphenol A (BPA) in food, paper, and personal care products. It is imperative to clarify the relationship between BPS and tumors in order to treat and prevent diseases. This study discovered a new method for predicti...

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Main Authors: Yi Wang, Jintian Song, Yangming Li, Chen Lin, Yan Chen, Xu Zhang, Hui Yu
Format: Article
Language:English
Published: Elsevier 2023-07-01
Series:Ecotoxicology and Environmental Safety
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0147651323005584
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author Yi Wang
Jintian Song
Yangming Li
Chen Lin
Yan Chen
Xu Zhang
Hui Yu
author_facet Yi Wang
Jintian Song
Yangming Li
Chen Lin
Yan Chen
Xu Zhang
Hui Yu
author_sort Yi Wang
collection DOAJ
description In recent years, Bisphenol S (BPS) has increasingly been used as an alternative to Bisphenol A (BPA) in food, paper, and personal care products. It is imperative to clarify the relationship between BPS and tumors in order to treat and prevent diseases. This study discovered a new method for predicting tumor correlations between BPS interactive genes. According to analyses conducted by Gene Ontology and Kyoto Encyclopedia of Genes and Genomes, interactive genes were primarily found in gastric cancer. Based on gene-targeted prediction and molecular docking, BPS appears to exert potential gastric cancer-causing effects through estrogen receptor 1 (ESR1). In addition, gastric cancer patients' prognosis could be accurately predicted by a bisphenol-based prognostic prediction model. Subsequently, the proliferation and migration abilities of gastric cancer cells were further demonstrated to be significantly enhanced by BPS. Similarly, molecular docking analysis revealed that melatonin is also highly correlated with gastric cancer and BPS. In cell proliferation and migration assays, melatonin and BPS exposure inhibited the invasion abilities of gastric cancer cells compared to BPS-exposure. Our research provided a new direction for the exploration the correlation between cancer and environmental toxicity.
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spelling doaj.art-620bbf410d25499bb7669a9aa562accb2023-06-03T04:21:36ZengElsevierEcotoxicology and Environmental Safety0147-65132023-07-01259115054Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1Yi Wang0Jintian Song1Yangming Li2Chen Lin3Yan Chen4Xu Zhang5Hui Yu6Department of Gastrointestinal Surgical Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou 350000, Fujian Province, ChinaDepartment of Abdominal Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou 350000, Fujian Province, ChinaDepartment of Gastrointestinal Surgical Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou 350000, Fujian Province, ChinaSchool of Pharmacy, Fujian Medical University, Fuzhou 350000, Fujian Province, ChinaSchool of Pharmacy, Fujian Medical University, Fuzhou 350000, Fujian Province, ChinaNanjing Medical University, Nanjing, 210029, ChinaDepartment of Pharmacy, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou 350000, Fujian Province, China; Corresponding author.In recent years, Bisphenol S (BPS) has increasingly been used as an alternative to Bisphenol A (BPA) in food, paper, and personal care products. It is imperative to clarify the relationship between BPS and tumors in order to treat and prevent diseases. This study discovered a new method for predicting tumor correlations between BPS interactive genes. According to analyses conducted by Gene Ontology and Kyoto Encyclopedia of Genes and Genomes, interactive genes were primarily found in gastric cancer. Based on gene-targeted prediction and molecular docking, BPS appears to exert potential gastric cancer-causing effects through estrogen receptor 1 (ESR1). In addition, gastric cancer patients' prognosis could be accurately predicted by a bisphenol-based prognostic prediction model. Subsequently, the proliferation and migration abilities of gastric cancer cells were further demonstrated to be significantly enhanced by BPS. Similarly, molecular docking analysis revealed that melatonin is also highly correlated with gastric cancer and BPS. In cell proliferation and migration assays, melatonin and BPS exposure inhibited the invasion abilities of gastric cancer cells compared to BPS-exposure. Our research provided a new direction for the exploration the correlation between cancer and environmental toxicity.http://www.sciencedirect.com/science/article/pii/S0147651323005584ESR1Gastric cancerBisphenol SMelatoninMolecular docking
spellingShingle Yi Wang
Jintian Song
Yangming Li
Chen Lin
Yan Chen
Xu Zhang
Hui Yu
Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1
Ecotoxicology and Environmental Safety
ESR1
Gastric cancer
Bisphenol S
Melatonin
Molecular docking
title Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1
title_full Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1
title_fullStr Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1
title_full_unstemmed Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1
title_short Melatonin inhibited the progression of gastric cancer induced by Bisphenol S via regulating the estrogen receptor 1
title_sort melatonin inhibited the progression of gastric cancer induced by bisphenol s via regulating the estrogen receptor 1
topic ESR1
Gastric cancer
Bisphenol S
Melatonin
Molecular docking
url http://www.sciencedirect.com/science/article/pii/S0147651323005584
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