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Bladder cancer associated transcript 1 (BLACAT1) is a long non-coding RNA (lncRNA) of more than 200 nucleotides, lacking protein-coding capacity, and primarily nuclear in localization[1][2]. It regulates gene expression at the transcriptional and epigenetic levels, often through interaction with the polycomb repressive complex 2 (PRC2), leading to the trimethylation of histone H3 lysine 27 (H3K27me3) and silencing of tumor suppressor genes such as p15[1][2]. BLACAT1 is aberrantly overexpressed in multiple cancers and consistently associated with tumor progression, metastasis, and poor prognosis[1][2]. Its depletion results in decreased proliferation, increased apoptosis, and reduced metastatic ability in cancer models. Currently, BLACAT1 is considered a promising prognostic biomarker and a potential, though still preclinical, therapeutic target in oncology[1][2].
Not applicable (no direct-acting drugs known). Antisense RNA/lncRNA-targeting approaches could downregulate BLACAT1, resulting in reduced proliferation and increased apoptosis in cancer cells[1][2].
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