Jariani Abbas, Kakroodi Setareh Talebi, Arabfard Masoud, Jamialahmadi Tannaz, Rahimi Maryam, Sahebkar Amirhossein
Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Pars Pathobiology Laboratory, Chalus, Mazandaran, Iran.
Curr Med Chem. 2024;31(12):1595-1605. doi: 10.2174/0929867330666230331101458.
Angiogenesis involves the development of new blood vessels. Biochemical signals start this process in the body, which is followed by migration, growth, and differentiation of endothelial cells that line the inside wall of blood vessels. This process is vital for the growth of cancer cells and tumors.
We started our analysis by composing a list of genes that have a validated impact in humans with respect to angiogenesis-related phenotypes. Here, we have investigated the expression patterns of angiogenesis-related genes in the context of previously published single-cell RNA-Seq data from prostate and breast cancer samples.
Using a protein-protein interaction network, we showed how different modules of angiogenesis-related genes are overexpressed in different cell types. In our results, genes, such as ACKR1, AQP1, and EGR1, showed a strong cell type-dependent overexpression pattern in the two investigated cancer types, which can potentially be helpful in the diagnosis and follow-up of patients with prostate and breast cancer.
Our work demonstrates how different biological processes in distinct cell types contribute to the angiogenesis process, which can provide clues regarding the potential application of targeted inhibition of the angiogenesis process.
血管生成涉及新血管的发育。生化信号在体内启动这一过程,随后是血管内皮层细胞的迁移、生长和分化。这个过程对癌细胞和肿瘤的生长至关重要。
我们首先列出了在人类中与血管生成相关表型有验证影响的基因列表。在这里,我们研究了血管生成相关基因在前列腺癌和乳腺癌样本先前发表的单细胞 RNA-Seq 数据背景下的表达模式。
使用蛋白质-蛋白质相互作用网络,我们展示了血管生成相关基因的不同模块如何在不同的细胞类型中过度表达。在我们的结果中,ACKR1、AQP1 和 EGR1 等基因在两种研究的癌症类型中表现出强烈的细胞类型依赖性过表达模式,这可能有助于前列腺癌和乳腺癌患者的诊断和随访。
我们的工作表明,不同细胞类型中的不同生物学过程如何促进血管生成过程,这可能为靶向抑制血管生成过程的潜在应用提供线索。