ArticleTranslational cancer research2026
A ferroptosis-related competing endogenous RNA network: HOX transcript antisense intergenic RNA/miR-129-5p/brain and acute leukemia, cytoplasmic axis contributes to the malignant progression of esophageal squamous cell carcinoma.
Article in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Esophageal squamous cell carcinoma (ESCC) is a leading cause of cancer-related mortality globally, characterized by high incidence, poor prognosis, and limited therapeutic options. While long non-coding RNAs (lncRNAs) and microRNAs have been implicated in ESCC pathogenesis through competing endogenous RNA (ceRNA) networks, the regulatory mechanisms underlying ferroptosis-related ceRNA interactions remain poorly defined. This study aimed to elucidate the functional role and molecular mechanism of the HOX transcript antisense intergenic RNA (HOTAIR)/miR-129-5p/brain and acute leukemia, cytoplasmic (BAALC) axis in ESCC progression. Methods: The regulatory relationship within the HOTAIR/miR-129-5p/ Results: Inhibition of Conclusions: This study unveils a novel ferroptosis-associated ceRNA regulatory axis in ESCC, demonstrating that HOTAIR promotes malignant progression by modulating the miR-129-5p/
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