2022
DOI: 10.1007/s00018-022-04350-x
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EIF4A3-induced circFIP1L1 represses miR-1253 and promotes radiosensitivity of nasopharyngeal carcinoma

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Cited by 11 publications
(3 citation statements)
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“…As reported in previous publications, miR-1253 knockdown can suppress NPC cell viability, accelerate NPC cell apoptosis and enhance the radiosensitivity of NPC. Mechanistically, upstream circFIP1L1 suppressed the inhibitory effect of miR-1253 on EIF4A3 ( 16 ). Moreover, miR-7-5p can reduce the radiosensitivity of NPC cells by promoting cell proliferation and accelerating cell death through the upregulation of ENO2 ( 18 ).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…As reported in previous publications, miR-1253 knockdown can suppress NPC cell viability, accelerate NPC cell apoptosis and enhance the radiosensitivity of NPC. Mechanistically, upstream circFIP1L1 suppressed the inhibitory effect of miR-1253 on EIF4A3 ( 16 ). Moreover, miR-7-5p can reduce the radiosensitivity of NPC cells by promoting cell proliferation and accelerating cell death through the upregulation of ENO2 ( 18 ).…”
Section: Resultsmentioning
confidence: 99%
“…Several scholars have identified and demonstrated the impact of miRNAs in adjusting the differential expression of functional genes on cell proliferation, invasion, apoptosis, migration, and even novel phenotypes in NPC against the background of radiation resistance and chemotherapy resistance (16)(17)(18)(19). Therefore, further exploration and validation of new miRNAs may lead to the identification of vital biomarkers or predictors for identifying radioresistant or chemo resistant patients in the clinic.…”
mentioning
confidence: 99%
“…METTL3 knockout decreased the stability of SOCS3, may owe to reduced m6A modi cations around their stop codons preferentially recognized and stabilized by IGF2BP1 [32][33][34] . Really, numerous studies suggest that IGF2BP1 selectively recognizes and promotes mRNA stability 35,36 . Our data demonstrated that m6A modi cation and SOCS3 are involved senescence of SkMSCs, suggesting that intervention of m6A modi cation and m6A might be a potential strategy for regulating cell senescence.…”
Section: Discussionmentioning
confidence: 99%