| Literature DB >> 34935097 |
Ying Li1, Ming-Qian Sun1, Lei Li1, Ye-Hao Zhang1, Lan Miao1, Jian-Xun Liu2.
Abstract
The abnormality of platelet function plays an important role in the pathogenesis and evolution of blood stasis syndrome (BSS). The explanation of its mechanism is a key scientific issue in the study of cardiovascular and cerebrovascular diseases and treatment. System biology technology provides a good technical platform for further development of platelet multi-omics, which is conducive to the scientific interpretation of the biological mechanism of BSS. The article summarized the pathogenesis of platelets in BSS, the mechanism of action of blood activating and stasis resolving drugs, and the application of genomics, proteomics, and metabonomics in platelet research, and put forward the concept of "plateletomics in BSS". Through the combination and cross-validation of multi-omics technology, it mainly focuses on the clinical and basic research of cardiovascular and cerebrovascular diseases; through the interactive verification of multi-omics technology and system biology, it mainly focuses on the platelet function and secretion system. The article systematically explains the molecular biological mechanism of platelet activation, aggregation, release, and other stages in the formation and development of BSS, and provides a new research idea and method for clarifying the pathogenesis of BSS and the mechanism of action of blood activating and stasis resolving drugs.Entities:
Keywords: blood stasis syndrome; metabonomics; platelet; proteomics; transcriptomics
Mesh:
Year: 2021 PMID: 34935097 DOI: 10.1007/s11655-021-3349-y
Source DB: PubMed Journal: Chin J Integr Med ISSN: 1672-0415 Impact factor: 1.978