2023
DOI: 10.1038/s41401-023-01143-1
|View full text |Cite
|
Sign up to set email alerts
|

Natural compound fraxinellone ameliorates intestinal fibrosis in mice via direct intervention of HSP47-collagen interaction in the epithelium

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(3 citation statements)
references
References 43 publications
0
3
0
Order By: Relevance
“…A direct binding of (4) to the purified protein has been evidenced by surface plasmon resonance (Kd = 3.542 × 10 −5 M), and a modeling analysis helped to define the location of the binding site with the implication of some key amino acids in the binding process, notably residues Tyr383 and Asp385. This drug interaction inhibits and destroys the complex between the chaperone Hsp47 and collagen, thereby perturbating procollagen folding and collagen processing [102]. The interaction with Hsp47 directly implicates the furan unit of fraxinellone.…”
Section: Potential Molecular Targets Of Prieurianin and Analogsmentioning
confidence: 99%
See 1 more Smart Citation
“…A direct binding of (4) to the purified protein has been evidenced by surface plasmon resonance (Kd = 3.542 × 10 −5 M), and a modeling analysis helped to define the location of the binding site with the implication of some key amino acids in the binding process, notably residues Tyr383 and Asp385. This drug interaction inhibits and destroys the complex between the chaperone Hsp47 and collagen, thereby perturbating procollagen folding and collagen processing [102]. The interaction with Hsp47 directly implicates the furan unit of fraxinellone.…”
Section: Potential Molecular Targets Of Prieurianin and Analogsmentioning
confidence: 99%
“…The regulation of Hsp47-collagen's interaction with fraxinellone accounts for the antifibrotic action of the limonoid [102], and it may also contribute to its antimetastatic activity because Hsp47 is a known stimulator of metastasis in solid tumors, notably in breast cancer [103]. These observations prompted us to consider that, by analogy, prieurianin could bind to Hsp47 via its fraxinellone-like moiety.…”
Section: Potential Molecular Targets Of Prieurianin and Analogsmentioning
confidence: 99%
“…In 2023, multiple studies were conducted to assess the effectiveness of existing management strategies and investigate potential new anti‐fibrotic treatments (Table 4 ). 23 , 73 , 74 , 75 , 76 , 77 , 78 , 80 , 81 , 82 , 83 …”
Section: Managementmentioning
confidence: 99%