| Literature DB >> 29967256 |
Zhen Xing1, Yanyan Zhang1, Ke Liang1, Liang Yan1, Yu Xiang2, Chunlai Li1, Qingsong Hu1, Feng Jin3, Vasanta Putluri3, Nagireddy Putluri3, Cristian Coarfa3, Arun Sreekumar3, Peter K Park1, Tina K Nguyen1, Shouyu Wang1,4, Jianwei Zhou4, Yan Zhou5, Jeffrey R Marks2, David H Hawke6, Mien-Chie Hung1,7,8, Liuqing Yang1,7,9, Leng Han10, Haoqiang Ying1,7, Chunru Lin11,7,9.
Abstract
Long noncoding RNA (lncRNA) is yet to be linked to cancer metabolism. Here, we report that upregulation of the lncRNA LINC00538 (YIYA) promotes glycolysis, cell proliferation, and tumor growth in breast cancer. YIYA is associated with the cytosolic cyclin-dependent kinase CDK6 and regulated CDK6-dependent phosphorylation of the fructose bisphosphatase PFK2 (PFKFB3) in a cell-cycle-independent manner. In breast cancer cells, these events promoted catalysis of glucose 6-phosphate to fructose-2,6-bisphosphate/fructose-1,6-bisphosphate. CRISPR/Cas9-mediated deletion of YIYA or CDK6 silencing impaired glycolysis and tumor growth in vivo In clinical specimens of breast cancer, YIYA was expressed in approximately 40% of cases where it correlated with CDK6 expression and unfavorable survival outcomes. Our results define a functional role for lncRNA in metabolic reprogramming in cancer, with potential clinical implications for its therapeutic targeting.Significance: These findings offer a first glimpse into how a long-coding RNA influences cancer metabolism to drive tumor growth. Cancer Res; 78(16); 4524-32. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 29967256 PMCID: PMC6126676 DOI: 10.1158/0008-5472.CAN-17-0385
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701