Muhamad Fikri Shazlan Saad, Muhammad Nazrul Hakim Abdullah, Vuanghao Lim, Hasnah Bahari, Boon Yin Khoo, Jun Jie Tan, Yoke Keong Yong
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Thirty male rats were grouped (n = 6) as follows: N (normal diet), NC (normal diet + CRC), HC (high-fat diet + CRC), NCB (normal diet + CRC + BPA), and HCB (high-fat diet + CRC + BPA). CRC was induced with 1,2-dimethylhydrazine (40 mg/kg), and BPA (25 mg/kg) was administered for 19 weeks. Although BPA exposure did not affect body weight or biochemical parameters, the HCB group exhibited significant histopathological changes in the colon, including lymphoid hyperplasia, liver damage, and increased IL-1β levels. Furthermore, diet influenced adipocyte size, exacerbating BPA's effects on CRC progression. Findings suggest BPA may worsen CRC progression in obese rats through identified pathways, promoting multi-organ pathology and underscoring the need for stricter regulations, especially for vulnerable populations. 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引用次数: 0
摘要
双酚A (BPA)是一种内分泌干扰物,与雌激素应答组织的癌症进展有关,但其在肥胖背景下促进结直肠癌(CRC)进展的作用仍未得到充分研究。本研究采用网络毒理学和实验模型研究了BPA对肥胖大鼠结直肠癌的影响。使用Database for Annotation, Visualization, and Integrated Discovery进行计算分析,确定了“CRC”和“化学致癌-受体激活”等通路,暗示PI3K-AKT通路参与IL-1 β上调和BPA在肥胖期间CRC中的作用。30只雄性大鼠(n = 6)分为:n(正常饮食)、NC(正常饮食+结直肠癌)、HC(高脂饮食+结直肠癌)、NCB(正常饮食+结直肠癌 + BPA)和HCB(高脂饮食+结直肠癌 + BPA)。1,2-二甲基肼(40 mg/kg)和BPA(25 mg/kg)诱导结直肠癌19 周。尽管BPA暴露不影响体重或生化参数,但HCB组在结肠中表现出显著的组织病理学变化,包括淋巴样增生、肝损伤和IL-1β水平升高。此外,饮食影响脂肪细胞大小,加剧了BPA对结直肠癌进展的影响。研究结果表明,BPA可能通过确定的途径恶化肥胖大鼠的结直肠癌进展,促进多器官病理,并强调需要更严格的法规,特别是对弱势群体。环境影响:双酚A (BPA)是一种广泛存在的环境污染物,在易感人群中与包括癌症在内的严重健康问题联系越来越紧密。我们的研究强调了BPA在促进肥胖驱动的结直肠癌(CRC)进展中的作用,证明了其在高风险环境中的致癌潜力。这些发现强调了对BPA暴露进行监管审查的迫切需要,特别是在肥胖人群中,并支持开发更安全的替代品。解决双酚a的影响有助于制定预防保健战略,并为旨在减少与内分泌干扰化学品有关的环境和公众健康风险的政策提供信息。
Exploring the role of Bisphenol A in obesity-driven colorectal cancer progression: network toxicology and multi-organ pathology in animal models.
Bisphenol A (BPA), an endocrine disruptor, is linked to cancer progression in estrogen-responsive tissues, but its role in promoting colorectal cancer (CRC) progression in the context of obesity remains underexplored. This study examines BPA's influence on CRC in obese Sprague-Dawley rats using network toxicology and experimental models. Computational analysis using the Database for Annotation, Visualization, and Integrated Discovery identified pathways such as "CRC" and "chemical carcinogenesis-receptor activation", implicating the PI3K-AKT pathway in IL-1 beta upregulation and BPA's role in CRC during obesity. Thirty male rats were grouped (n = 6) as follows: N (normal diet), NC (normal diet + CRC), HC (high-fat diet + CRC), NCB (normal diet + CRC + BPA), and HCB (high-fat diet + CRC + BPA). CRC was induced with 1,2-dimethylhydrazine (40 mg/kg), and BPA (25 mg/kg) was administered for 19 weeks. Although BPA exposure did not affect body weight or biochemical parameters, the HCB group exhibited significant histopathological changes in the colon, including lymphoid hyperplasia, liver damage, and increased IL-1β levels. Furthermore, diet influenced adipocyte size, exacerbating BPA's effects on CRC progression. Findings suggest BPA may worsen CRC progression in obese rats through identified pathways, promoting multi-organ pathology and underscoring the need for stricter regulations, especially for vulnerable populations. ENVIRONMENTAL IMPLICATION: Bisphenol A (BPA), a widespread environmental contaminant, is increasingly linked to serious health issues, including cancer, in susceptible populations. Our study highlights BPA's role in promoting obesity-driven colorectal cancer (CRC) progression, demonstrating its carcinogenic potential in high-risk contexts. These findings emphasize the urgent need for regulatory scrutiny of BPA exposure, particularly in obese individuals, and support the development of safer alternatives. Addressing BPA's impact can contribute to preventive health strategies and inform policies aimed at reducing environmental and public health risks associated with endocrine-disrupting chemicals.
期刊介绍:
Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products.
Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged.
Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.