| Literature DB >> 36149588 |
Swastika Maitra1, Biswajit Chakraborty2, Sumira Malik3, Athanasios Alexiou4,5, Nobendu Mukerjee6,7, Subhradeep Roy8, Shaswata Modak8, Mohammad Mehedi Hasan9, Arabinda Ghosh10, Asmita Ghosh11, Mohammad Amjad Kamal12,13,14,15, Abhijit Dey16, Ghulam Md Ashraf17,18, Md Habibur Rahman19, Badrah S Alghamdi17,20, Adel Mohammad Abuzenadah13,21.
Abstract
Glioblastoma (GB) are aggressive tumors that obstruct normal brain function. While the skull cannot expand in response to cancer growth, the growing pressure in the brain is generally the first sign. It can produce more frequent headaches, unexplained nausea or vomiting, blurred peripheral vision, double vision, a loss of feeling or movement in an arm or leg, and difficulty speaking and concentrating; all depend on the tumor's location. GB can also cause vascular thrombi, damaging endothelial cells and leading to red blood cell leakage. Latest studies have revealed the role of single nucleotide polymorphisms (SNPs) in developing and spreading cancers such as GB and breast cancer. Many discovered SNPs are associated with GB, particularly in great abundance in the promoter region, creating polygenetic vulnerability to glioma. This study aims to compile a list of some of the most frequent and significant SNPs implicated with GB formation and proliferation.Entities:
Keywords: Epidermal growth factors receptor; Glioblastoma; Single nucleotide polymorphisms; Tumors
Year: 2022 PMID: 36149588 DOI: 10.1007/s11011-022-01082-6
Source DB: PubMed Journal: Metab Brain Dis ISSN: 0885-7490 Impact factor: 3.655