2020
DOI: 10.3892/or.2020.7500
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Long non‑coding RNA CCAT1 enhances human non‑small cell lung cancer growth through downregulation of microRNA‑218

Abstract: Long non-coding RNAs (lncRNAs) have critical functions in non-small cell lung cancer (NSCLC) growth. In the present study, we showed that lncRNA-CCAT1 was upregulated in NSCLC tissues. High expression of lncRNA-CCAT1 was related to tumor growth and reduced survival rate. We used short hairpin RNAs (shRNAs) to inhibit the expression of lncRNA-CCAT1 in NSCLC cells. In vitro and in vivo results demonstrated that lncRNA-CCAT1 knockdown suppressed tumor proliferation and induced apoptosis. Furthermore, microRNA-218… Show more

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Cited by 6 publications
(8 citation statements)
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References 27 publications
(23 reference statements)
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“…25 In consistency with the previous finding, we also observed significantly higher CCAT1 expression in NSCLC cells than in human bronchial epithelial cell 16HBE. 8 Actually, CCAT1 was located around the proto-oncogene c-Myc, thus possibly contributing to upregulate its expression. 26 Similarly, the expression level of CCAT1 in radioresistant breast cancer tissues was remarkably higher than that in radiosensitive breast cancer tissues.…”
Section: Effects Of Ccat1 On the Radiosensitivity Of Nsclc Cells May Be Related To Mapk Signaling Pathwaymentioning
confidence: 99%
See 2 more Smart Citations
“…25 In consistency with the previous finding, we also observed significantly higher CCAT1 expression in NSCLC cells than in human bronchial epithelial cell 16HBE. 8 Actually, CCAT1 was located around the proto-oncogene c-Myc, thus possibly contributing to upregulate its expression. 26 Similarly, the expression level of CCAT1 in radioresistant breast cancer tissues was remarkably higher than that in radiosensitive breast cancer tissues.…”
Section: Effects Of Ccat1 On the Radiosensitivity Of Nsclc Cells May Be Related To Mapk Signaling Pathwaymentioning
confidence: 99%
“…For example, CCAT1 knockdown in prostate cancer can hinder the survival and reduce the half maximal inhibitory concentration (IC50) of paclitaxel (PTX), but enhance the apoptosis rate of PC3-TXR and DU145-TXR cells treated with PTX. 28 Of note, CCAT1 gene deletion can induce the apoptosis of human NSCLC cells, 8 and further increase the apoptosis of NSCLC cells induced by gefitinib. 20 On the other hand, it has also been shown a correlation of the radiosensitivity of tumor cells with cell cycle.…”
Section: Effects Of Ccat1 On the Radiosensitivity Of Nsclc Cells May Be Related To Mapk Signaling Pathwaymentioning
confidence: 99%
See 1 more Smart Citation
“…Chen et al identified the oncogene function of CCAT1 and induce chemoresistance in docetaxel resistant NSCLC cells 26 . Zhao et al shown that the upregulated CCAT1 in NSCLC cells was involved in the poor prognosis in NSCLC and knockdown of CCAT1 induces apoptosis and inhibits progression by targeting the miR‐218/BMI‐1 axis in NSCLC cells 27 …”
Section: Introductionmentioning
confidence: 99%
“…Zhao's study found that lncRNA-CCAT1 knockdown suppressed tumor proliferation and induced apoptosis. High expression of lncRNA-CCAT1 was related to tumor growth and reduced survival rate, which can be a novel marker for lung cancer[29]. Ju's study systematically found prognosis-related lncRNAs, miRNAs, and mRNAs and constructed a prognosis-related competing endogenous RNA network[30].…”
mentioning
confidence: 99%