2017
DOI: 10.1007/s10529-016-2273-2
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MicroRNA-190b confers radio-sensitivity through negative regulation of Bcl-2 in gastric cancer cells

Abstract: miR-190b confers radio-sensitivity of GC cells, possibly via negative regulation of Bcl-2.

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Cited by 17 publications
(25 citation statements)
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“…25 Wang et al demonstrated that miR-190b enhanced the radio-sensitivity of GC cells through negatively regulated Bcl-2. 26 Ding et al revealed that miR-27a stimulated the tumorgenesis of GC by activating the AKT/GSK3b pathway. 27 Mi et al validated that miR-181a-5p facilitated the development of GC via RASSF6-modulated MAPK signaling pathway.…”
Section: Discussionmentioning
confidence: 99%
“…25 Wang et al demonstrated that miR-190b enhanced the radio-sensitivity of GC cells through negatively regulated Bcl-2. 26 Ding et al revealed that miR-27a stimulated the tumorgenesis of GC by activating the AKT/GSK3b pathway. 27 Mi et al validated that miR-181a-5p facilitated the development of GC via RASSF6-modulated MAPK signaling pathway.…”
Section: Discussionmentioning
confidence: 99%
“…40 Current therapeutic strategies were considered to optimize radiosensitivity of GC to F I G U R E 4 Elevated expression of lincRNA-p21 suppressed the GC cell cycle and migration. [42][43][44] The molecular mechanism of radiosensitivity in the GC is still unknown. B, Ectopic expression of lincRNA-p21 suppressed the SGC7901 cell cycle.…”
Section: Discussionmentioning
confidence: 99%
“…C5b9, LDH, TnI, and CK-MB are important burn injury-induced myocardial infarction markers, and their diagnostic utility in patients with myocardial infarctions has been established [26,27]. miR-190b, which can be detected in tissues and blood in human, is an oncogene that promotes tumorigenesis in several cancers through the regulation of genes, such as Bcl-2, PTEN, and IGF-1 [28][29][30]. miR-190b promotes cell proliferation, invasion, and migration but decreases cell apoptosis [30].…”
Section: Discussionmentioning
confidence: 99%