2017
DOI: 10.1158/0008-5472.can-16-1615
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Long Noncoding RNA LINC00092 Acts in Cancer-Associated Fibroblasts to Drive Glycolysis and Progression of Ovarian Cancer

Abstract: The majority of patients with epithelial ovarian cancer are diagnosed at a late stage when the peritoneal metastases exist; however, there is little knowledge of the metastatic process in this disease setting. In this study, we report the identification of the long noncoding RNA LINC00092 as a nodal driver of metastatic progression mediated by cancer-associated fibroblasts (CAF). Prometastatic properties of CAFs and were found to associate with elevated expression of the chemokine CXCL14. In clinical specimens… Show more

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Cited by 199 publications
(160 citation statements)
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“…Another study indicated that colorectal neoplasia differentially expressed ( CRNDE ) nuclear transcripts upregulated in colorectal cancer were involved in the regulation of cell metabolism [45]. Zhao et al reported that LINC00092 promoted metastasis by altering glycolysis and sustaining the local supportive function of cancer-associated fibroblasts (CAFs) through binding to glycolytic enzyme-the fructose-2,6-biphosphatase PFKFB2 [46]. Knockdown lncRNA ceruloplasmin (NRCP) could significantly decrease glycolysis and increases mitochondrial respiration in ovarian cancer cells [47].…”
Section: Discussionmentioning
confidence: 99%
“…Another study indicated that colorectal neoplasia differentially expressed ( CRNDE ) nuclear transcripts upregulated in colorectal cancer were involved in the regulation of cell metabolism [45]. Zhao et al reported that LINC00092 promoted metastasis by altering glycolysis and sustaining the local supportive function of cancer-associated fibroblasts (CAFs) through binding to glycolytic enzyme-the fructose-2,6-biphosphatase PFKFB2 [46]. Knockdown lncRNA ceruloplasmin (NRCP) could significantly decrease glycolysis and increases mitochondrial respiration in ovarian cancer cells [47].…”
Section: Discussionmentioning
confidence: 99%
“…It inhibits one of the glycolytic enzymes, fructose-2,6-bisphosphatase (PFKFB2), thereby altering glycolysis, which in turn promotes metastasis and sustains the local supportive function of cancer-associated fibroblasts (CAFs) [4750] (Fig. 1).…”
Section: Lncrnas Regulate Enzymes Regulatory Molecules and Oncogenementioning
confidence: 99%
“…As indicated in Fig. 1B, the glycolysis-regulatory molecules, fructose-2 and 6-biphosphatase (PFKFB2), bind to the binding site of LINC00092, leading to a reciprocal regulatory loop with CAFs by controlling glycolytic products to maintain the tumor environment and subsequently cancer metastasis [40].…”
Section: Involvement Of Lncrnas In Ocmentioning
confidence: 99%