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MicroRNA 105-2 (MIR105-2, hsa-mir-105-2) is a short non-coding RNA molecule classified as a microRNA, located on human chromosome Xq28[2][4]. It is one of a small family (miR-105-1, miR-105-2, and miR-767)[2]. It regulates gene expression post-transcriptionally by binding to partially complementary sequences in target mRNAs, leading to translational repression or mRNA degradation[4][6]. MIR105-2 has context-dependent roles in cancer, functioning as either a tumor suppressor or an oncogene depending on tissue type and cellular context[2]. It is implicated in several cancer types, influencing processes such as tumor growth, metastasis, epithelial-mesenchymal transition, apoptosis, and chemoresistance. Upregulation or downregulation of miR-105 levels can serve as a prognostic or diagnostic biomarker in diseases such as multiple myeloma, triple-negative breast cancer, hepatocellular carcinoma, and gliomas[1][2][3]. Therapeutic targeting is still experimental, focusing on modulation of miR-105 activity rather than direct drug antagonism, and raises specific safety concerns typical of interventions affecting broad gene regulatory networks.
Not applicable (microRNAs themselves are gene regulators and not protein targets for binding by conventional drugs; therapeutic approaches are primarily based on modulation of miRNA levels using mimics, inhibitors, or antisense oligonucleotides)
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