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HOXB cluster antisense RNA 1 (HOXB-AS1) is a long non-coding RNA (lncRNA) transcribed antisense to the HOXB gene cluster, particularly located between HOXB2 and HOXB3[1][3]. It does not encode a protein but acts as a regulator in gene expression at both the transcriptional and post-transcriptional levels. HOXB-AS1 is overexpressed in several tumor types, most notably in glioblastoma, endometrial carcinoma, and multiple myeloma, where it is linked to cancer proliferation, invasion, stem cell maintenance, and poor prognosis[2][4][1]. Mechanistically, HOXB-AS1 interacts with proteins (such as ILF3) to increase HOXB2 and HOXB3 gene expression and acts as a sponge for various microRNAs, contributing to oncogenic pathways such as Wnt signaling[2][4]. It can serve as a prognostic biomarker in cancer but does not have any currently approved drug interactions or established therapies targeting it. Safety concerns mainly relate to its key role in oncogenesis; modulating its function may disrupt normal developmental or stem cell processes and could entail risks of unwanted gene regulatory changes.
lncRNA–protein scaffold (recruits ILF3 for gene transcription regulation), Competitive endogenous RNA (sponges miR-186-5p, miR-149-3p, miR-885-3p), Stabilizes mRNA (HOXB2, HOXB3, FUT4), Activates Wnt signaling pathway
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