2022
DOI: 10.1007/s11262-021-01882-5
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Epstein–Barr virus miR-BART4-3p regulates cell proliferation, apoptosis, and migration by targeting AXL in gastric carcinoma

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Cited by 4 publications
(4 citation statements)
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“…In this experiment, 5 µL of the exosome/LMP1 complex from an NPC patient serum (SNPC) was used in a culture medium without FBS to test cell proliferation, as described previously [ 13 ]. The controls used were exosomes isolated from healthy individuals (EC-SNF), with or without FBS.…”
Section: Methodsmentioning
confidence: 99%
“…In this experiment, 5 µL of the exosome/LMP1 complex from an NPC patient serum (SNPC) was used in a culture medium without FBS to test cell proliferation, as described previously [ 13 ]. The controls used were exosomes isolated from healthy individuals (EC-SNF), with or without FBS.…”
Section: Methodsmentioning
confidence: 99%
“…Additional EBV-encoded miRNAs contribute to immune escape through diverse mechanisms. For instance, miR-BART4-3p exerts a multifaceted influence on gastric carcinoma cells by regulating proliferation, apoptosis, and migration ( 50 ). Similarly, miR-BART4-5p promotes immune evasion by downregulating proapoptotic proteins, thereby reducing apoptosis in gastric cancer cells ( 51 ).…”
Section: The Elusive Escape Artist: Unraveling Ebv’s Art Of Immune Ev...mentioning
confidence: 99%
“…In EBVaGC cells, EBV-encoded miRNAs modulate epithelialmesenchymal transition (EMT), affecting intercellular adhesion and cell motility and deformability, leading to alterations in the migration capability of the tumor cells (32). Meng-He Zhao and colleagues revealed that miR-BART4-3P targeted the AXL gene directly to promote the apoptosis and suppress the proliferation and migration of GC cells via downstream effectors of EMT, including E-cadherin, Vimentin, Zinc Finger E-box Binding Homeobox 1 (ZEB1), and phospho-AKT (P-AKT) (33). Besides, Juanjuan Liu et al reported that miR-BART1-5p restrained GC cells proliferation and migration by targeting GCNT3 (core 2b-1, 6-acetylglucosaminyltransferase) via modulating the expressions of E-cadherin, N-cadherin, and Vimentin (34).…”
Section: Migrationmentioning
confidence: 99%