Suppr超能文献

从蛋白质-蛋白质相互作用网络中鉴定与细胞凋亡相关的新型候选基因。

Identifying Novel Candidate Genes Related to Apoptosis from a Protein-Protein Interaction Network.

作者信息

Wang Baoman, Yuan Fei, Kong Xiangyin, Hu Lan-Dian, Cai Yu-Dong

机构信息

Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

College of Life Science, Shanghai University, Shanghai 200444, China.

出版信息

Comput Math Methods Med. 2015;2015:715639. doi: 10.1155/2015/715639. Epub 2015 Oct 4.

Abstract

Apoptosis is the process of programmed cell death (PCD) that occurs in multicellular organisms. This process of normal cell death is required to maintain the balance of homeostasis. In addition, some diseases, such as obesity, cancer, and neurodegenerative diseases, can be cured through apoptosis, which produces few side effects. An effective comprehension of the mechanisms underlying apoptosis will be helpful to prevent and treat some diseases. The identification of genes related to apoptosis is essential to uncover its underlying mechanisms. In this study, a computational method was proposed to identify novel candidate genes related to apoptosis. First, protein-protein interaction information was used to construct a weighted graph. Second, a shortest path algorithm was applied to the graph to search for new candidate genes. Finally, the obtained genes were filtered by a permutation test. As a result, 26 genes were obtained, and we discuss their likelihood of being novel apoptosis-related genes by collecting evidence from published literature.

摘要

细胞凋亡是多细胞生物中发生的程序性细胞死亡(PCD)过程。这种正常的细胞死亡过程对于维持体内平衡至关重要。此外,一些疾病,如肥胖症、癌症和神经退行性疾病,可以通过细胞凋亡来治愈,且副作用很小。有效理解细胞凋亡的潜在机制将有助于预防和治疗某些疾病。识别与细胞凋亡相关的基因对于揭示其潜在机制至关重要。在本研究中,提出了一种计算方法来识别与细胞凋亡相关的新候选基因。首先,利用蛋白质-蛋白质相互作用信息构建加权图。其次,将最短路径算法应用于该图以搜索新的候选基因。最后,通过置换检验对获得的基因进行筛选。结果,获得了26个基因,我们通过收集已发表文献中的证据来讨论它们作为新的细胞凋亡相关基因的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e5/4620916/2c3d5cea7770/CMMM2015-715639.001.jpg

相似文献

1
Identifying Novel Candidate Genes Related to Apoptosis from a Protein-Protein Interaction Network.
Comput Math Methods Med. 2015;2015:715639. doi: 10.1155/2015/715639. Epub 2015 Oct 4.
3
Mining for novel tumor suppressor genes using a shortest path approach.
J Biomol Struct Dyn. 2016;34(3):664-75. doi: 10.1080/07391102.2015.1042915. Epub 2015 Nov 30.
6
Mining for genes related to choroidal neovascularization based on the shortest path algorithm and protein interaction information.
Biochim Biophys Acta. 2016 Nov;1860(11 Pt B):2740-9. doi: 10.1016/j.bbagen.2016.03.015. Epub 2016 Mar 14.
7
Identifying novel protein phenotype annotations by hybridizing protein-protein interactions and protein sequence similarities.
Mol Genet Genomics. 2016 Apr;291(2):913-34. doi: 10.1007/s00438-015-1157-9. Epub 2016 Jan 4.
8
Discovery of new candidate genes related to brain development using protein interaction information.
PLoS One. 2015 Jan 30;10(1):e0118003. doi: 10.1371/journal.pone.0118003. eCollection 2015.
10
A network-based method for the identification of putative genes related to infertility.
Biochim Biophys Acta. 2016 Nov;1860(11 Pt B):2716-24. doi: 10.1016/j.bbagen.2016.04.010. Epub 2016 Apr 19.

引用本文的文献

1
Targeting cardiotoxicity: the potential of L. in doxorubicin therapy.
In Silico Pharmacol. 2025 Mar 17;13(1):47. doi: 10.1007/s40203-025-00333-5. eCollection 2025.
2
Integrated bioinformatics analysis of core regulatory elements involved in keloid formation.
BMC Med Genomics. 2021 Oct 2;14(1):239. doi: 10.1186/s12920-021-01087-7.
4
6
Identifying novel fruit-related genes in Arabidopsis thaliana based on the random walk with restart algorithm.
PLoS One. 2017 May 4;12(5):e0177017. doi: 10.1371/journal.pone.0177017. eCollection 2017.

本文引用的文献

2
Galangin suppresses HepG2 cell proliferation by activating the TGF-β receptor/Smad pathway.
Toxicology. 2014 Dec 4;326:9-17. doi: 10.1016/j.tox.2014.09.010. Epub 2014 Sep 28.
4
The TORC1 inhibitors Nprl2 and Nprl3 mediate an adaptive response to amino-acid starvation in Drosophila.
Cell Death Differ. 2014 Sep;21(9):1460-8. doi: 10.1038/cdd.2014.63. Epub 2014 May 2.
5
Cell deaths in normal vertebrate ontogeny.
Biol Rev Camb Philos Soc. 1951 Feb;26(1):59-86. doi: 10.1111/j.1469-185x.1951.tb00774.x.
7
TAK1 regulates hepatic cell survival and carcinogenesis.
J Gastroenterol. 2014 Feb;49(2):185-94. doi: 10.1007/s00535-013-0931-x. Epub 2014 Jan 21.
8
Protein tyrosine phosphatase 1B inhibition ameliorates palmitate-induced mitochondrial dysfunction and apoptosis in skeletal muscle cells.
Free Radic Biol Med. 2013 Dec;65:1435-1446. doi: 10.1016/j.freeradbiomed.2013.09.019. Epub 2013 Oct 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验