| Literature DB >> 28985503 |
Jin-Zhou Huang1, Min Chen2, Xing-Cheng Gao3, Song Zhu2, Hongyang Huang3, Min Hu2, Huifang Zhu2, Guang-Rong Yan4.
Abstract
A substantial fraction of eukaryotic transcripts are considered long non-coding RNAs (lncRNAs), which regulate various hallmarks of cancer. Here, we discovered that the lncRNA HOXB-AS3 encodes a conserved 53-aa peptide. The HOXB-AS3 peptide, not lncRNA, suppresses colon cancer (CRC) growth. Mechanistically, the HOXB-AS3 peptide competitively binds to the ariginine residues in RGG motif of hnRNP A1 and antagonizes the hnRNP A1-mediated regulation of pyruvate kinase M (PKM) splicing by blocking the binding of the ariginine residues in RGG motif of hnRNP A1 to the sequences flanking PKM exon 9, ensuring the formation of lower PKM2 and suppressing glucose metabolism reprogramming. CRC patients with low levels of HOXB-AS3 peptide have poorer prognoses. Our study indicates that the loss of HOXB-AS3 peptide is a critical oncogenic event in CRC metabolic reprogramming. Our findings uncover a complex regulatory mechanism of cancer metabolism reprogramming orchestrated by a peptide encoded by an lncRNA.Entities:
Keywords: PKM splicing; cancer metabolism; colon cancer; lncRNA; peptide
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Year: 2017 PMID: 28985503 DOI: 10.1016/j.molcel.2017.09.015
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970