2019
DOI: 10.1016/j.ejphar.2019.03.002
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LncRNA FAM83H-AS1 contributes to the radioresistance, proliferation, and metastasis in ovarian cancer through stabilizing HuR protein

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Cited by 48 publications
(43 citation statements)
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“…For example, FAM83H-AS1 could ameliorate SpA-mediated inhibition on the osteogenic differentiation of human bone mesenchymal stem cells during osteomyelitis and promote nucleus pulposus cell growth in intervertebral disc degeneration [28,29]. However, many studies recently showed that FAM83H-AS1 was overexpressed in some tumors and exhibited an oncogenic role in cell proliferation and metastasis [6,10,16]. Dou's study showed that elevated FAM83H-AS1 expression was correlated with radioresistance and poor OS and was used to effectively predict lymph node metastasis in ovarian cancer [16].…”
Section: Discussionmentioning
confidence: 99%
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“…For example, FAM83H-AS1 could ameliorate SpA-mediated inhibition on the osteogenic differentiation of human bone mesenchymal stem cells during osteomyelitis and promote nucleus pulposus cell growth in intervertebral disc degeneration [28,29]. However, many studies recently showed that FAM83H-AS1 was overexpressed in some tumors and exhibited an oncogenic role in cell proliferation and metastasis [6,10,16]. Dou's study showed that elevated FAM83H-AS1 expression was correlated with radioresistance and poor OS and was used to effectively predict lymph node metastasis in ovarian cancer [16].…”
Section: Discussionmentioning
confidence: 99%
“…However, many studies recently showed that FAM83H-AS1 was overexpressed in some tumors and exhibited an oncogenic role in cell proliferation and metastasis [6,10,16]. Dou's study showed that elevated FAM83H-AS1 expression was correlated with radioresistance and poor OS and was used to effectively predict lymph node metastasis in ovarian cancer [16]. Previous studies confirmed that the expression of HuR was positively correlated with the expression of FAM83H-AS1.…”
Section: Discussionmentioning
confidence: 99%
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“…Despite great efforts to use these advances in the clinic, only six of the lncRNAs listed in Table S1 have been identified in OC patients' blood serum samples; namely, E2F4AS [117], FEZF1-AS1 [20], FLVCR1-AS1 [41], LINK-A [26], MLK7-AS1 [40] and aHIF [13], the last-named being isolated specifically from exosomes in the serum. MEG3 and MALAT1 are probably on the way to being added to the list since they have been identified in exosomes derived from OC cell lines [26,107]. Interestingly, the serum and tumor tissue levels of aHIF, FEZF1-AS1, FLVCR1-AS1, LINK-A, and MLK7-AS1 correlate positively, providing a proof of concept for the usefulness of lncRNAs in liquid biopsy.…”
Section: Platinum Salts Taxanesmentioning
confidence: 99%
“…Surveying the function of lncRNAs globally (Figure 2b), 120 are considered as oncogenes, 114 confirmed and six putative; and 29 are considered as tumor suppressor genes, 25 confirmed and four putative. SPRY-IT1 [26], MEG3 [122,123], XIST [54,99] and TTN-AS1 [65,124] statuses remain unclear because the shreds of evidence collected are ambiguous. The experimental data about TC0101686, TC0100223, TC0901107, and TC1500845 show only that they are transcriptionally activated by estrogens.…”
Section: Lncrnas Implicated In Oc Development and Progressionmentioning
confidence: 99%