{"title":"Synthesis and study on treatment mechanism of galactosyl metalloporphyrin targeting hepatocarcinoma","authors":"Wei Hu , Jie Zhou , Jing Huang , Yanhua Yu","doi":"10.1016/j.colsurfb.2025.114794","DOIUrl":null,"url":null,"abstract":"<div><div>Tetra-antennary galactosyl metalloporphyrin ZnTPPGal targeting hepatocarcinoma was synthesized. ZnTPPGal exhibited excellent fluorescent properties and high mortality (IC<sub>50</sub> 0.91 × 10<sup>−5</sup> M ± 2.59) to HepG2 cells, showing good potential in drug tracing and targeted therapy. Relative quantitation proteomics analysis revealed that ZnTPPGal induced 475 differentially expressed proteins (DEPs) including 174 upregulated and 301 downregulated (Ratio > 1.5 or < 0.67). ZnTPPGal could inhibit cell survival and activate apoptosis mainly through endoplasmic reticulum stress pathway and mitochondrial dependent pathway, while did not activate autophagy. Functional proteins of EGFR, ASK1, Cat D, Rho, JNK, RagB and Rheb could be used as potential candidate proteins for hepatocarcinoma treatment and drug development.</div></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"254 ","pages":"Article 114794"},"PeriodicalIF":5.4000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloids and Surfaces B: Biointerfaces","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927776525003017","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Tetra-antennary galactosyl metalloporphyrin ZnTPPGal targeting hepatocarcinoma was synthesized. ZnTPPGal exhibited excellent fluorescent properties and high mortality (IC50 0.91 × 10−5 M ± 2.59) to HepG2 cells, showing good potential in drug tracing and targeted therapy. Relative quantitation proteomics analysis revealed that ZnTPPGal induced 475 differentially expressed proteins (DEPs) including 174 upregulated and 301 downregulated (Ratio > 1.5 or < 0.67). ZnTPPGal could inhibit cell survival and activate apoptosis mainly through endoplasmic reticulum stress pathway and mitochondrial dependent pathway, while did not activate autophagy. Functional proteins of EGFR, ASK1, Cat D, Rho, JNK, RagB and Rheb could be used as potential candidate proteins for hepatocarcinoma treatment and drug development.
期刊介绍:
Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields.
Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication.
The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.