Self-Crosslinked Admicelle of Sodium Conjugated Linoleate@Nano-CaCO3 and Its Stimuli–Response to Ca2+/pH/CO2 Triple Triggers

Author(s):  
Khin Nyein Ei San ◽  
Tian Niu ◽  
Yun Fang ◽  
Hong Wang ◽  
Ye Fan ◽  
...  
Keyword(s):  
Author(s):  
Yanning Han ◽  
Tong Zhang ◽  
Xinyu Chen ◽  
Qiao Chen ◽  
Jingjun Hao ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Daniel Trejo Banos ◽  
Daniel L. McCartney ◽  
Marion Patxot ◽  
Lucas Anchieri ◽  
Thomas Battram ◽  
...  

Abstract Linking epigenetic marks to clinical outcomes improves insight into molecular processes, disease prediction, and therapeutic target identification. Here, a statistical approach is presented to infer the epigenetic architecture of complex disease, determine the variation captured by epigenetic effects, and estimate phenotype-epigenetic probe associations jointly. Implicitly adjusting for probe correlations, data structure (cell-count or relatedness), and single-nucleotide polymorphism (SNP) marker effects, improves association estimates and in 9,448 individuals, 75.7% (95% CI 71.70–79.3) of body mass index (BMI) variation and 45.6% (95% CI 37.3–51.9) of cigarette consumption variation was captured by whole blood methylation array data. Pathway-linked probes of blood cholesterol, lipid transport and sterol metabolism for BMI, and xenobiotic stimuli response for smoking, showed >1.5 times larger associations with >95% posterior inclusion probability. Prediction accuracy improved by 28.7% for BMI and 10.2% for smoking over a LASSO model, with age-, and tissue-specificity, implying associations are a phenotypic consequence rather than causal.


2021 ◽  
pp. 119005
Author(s):  
Liu Liu ◽  
Nicolas R. Tanguy ◽  
Ning Yan ◽  
Yiqiang Wu ◽  
Xiubo Liu ◽  
...  

2008 ◽  
Author(s):  
Xiang Zheng ◽  
Fujun Yang ◽  
Ming Zhang ◽  
Lianlian Jiao

Author(s):  
Zhen Luo ◽  
Yujuan Gao ◽  
Zhongyu Duan ◽  
Yu Yi ◽  
Hao Wang

Mitochondria are well known to serve as the powerhouse for cells and also the initiator for some vital signaling pathways. A variety of diseases are discovered to be associated with the abnormalities of mitochondria, including cancers. Thus, targeting mitochondria and their metabolisms are recognized to be promising for cancer therapy. In recent years, great efforts have been devoted to developing mitochondria-targeted pharmaceuticals, including small molecular drugs, peptides, proteins, and genes, with several molecular drugs and peptides enrolled in clinical trials. Along with the advances of nanotechnology, self-assembled peptide-nanomaterials that integrate the biomarker-targeting, stimuli-response, self-assembly, and therapeutic effect, have been attracted increasing interest in the fields of biotechnology and nanomedicine. Particularly, in situ mitochondria-targeted self-assembling peptides that can assemble on the surface or inside mitochondria have opened another dimension for the mitochondria-targeted cancer therapy. Here, we highlight the recent progress of mitochondria-targeted peptide-nanomaterials, especially those in situ self-assembly systems in mitochondria, and their applications in cancer treatments.


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