کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2580330 1561618 2014 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
An in silico toxicogenomics approach for inferring potential diseases associated with maleic acid
ترجمه فارسی عنوان
یک روش روان شناختی سمیوژنز برای تعیین بیماری های بالقوه مرتبط با اسید مورف است
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی


• The maleic acid-interacting proteins are identified from STITCH database.
• The proteins are utilized to infer diseases and pathways affected by maleic acid.
• QSAR models are utilized to predict the ADMET profile of maleic acid.
• The approach can identify potential risks of poorly characterized chemicals.

Maleic acid is a multi-functional chemical widely applied in the manufacturing of polymer products including food packaging. However, the contamination of maleic acid in modified starch has raised the concerns about the effects of chronic exposure to maleic acid on human health. This study proposed a novel toxicogenomics approach for inferring functions, pathways and diseases potentially affected by maleic acid on humans by using known interactions between maleic acid and proteins. Neuronal signal transmission and cell metabolism were identified to be most influenced by maleic acid in this study. The top disease categories inferred to be associated with maleic acid were mental disorder, nervous system diseases, cardiovascular diseases, and cancers. The results from the in silico analysis showed that maleic acid could penetrate the blood–brain barrier to affect the nervous system. Several functions and pathways were further analyzed and identified to give insights into the mechanisms of maleic acid-associated diseases. The toxicogenomics approach may offer both a better understanding of the potential risks of maleic-acid exposure to humans and a direction for future toxicological investigation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemico-Biological Interactions - Volume 223, 5 November 2014, Pages 38–44
نویسندگان
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