Molecular biology reports · 2026
ATP5F1B promotes breast cancer progression through ERK associated metabolic reprogramming.
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Lu Xuan, Li Ruiqing, Chen Jiejing, Zhou Qiwang
Аннотация
BACKGROUND: To systematically evaluate the prognostic significance of mitochondrial ATP synthase subunits in breast cancer and to investigate the clinical relevance, biological function, and metabolic role of ATP5F1B in breast cancer progression.
METHODS: Publicly available breast cancer transcriptomic profiles with matched clinical annotations were analyzed in a family-level screen of mitochondrial ATP synthase subunits. ATP5F1B was prioritized and was evaluated by loss- and gain-of-function assays in AU565 and HCC1428 cells. Differential expression and functional enrichment analyses were performed, and metabolic activity was assessed by extracellular acidification rate. Key genes and proteins were validated by qRT-PCR and Western blotting.
RESULTS: ATP5F1B was upregulated in tumor tissues and emerged as the only screened F1 subunit consistently associated with survival. High ATP5F1B expression was linked to poorer overall survival, disease-specific survival, and progression-free interval, and correlated with clinicopathologic features, including age, estrogen receptor status, and PAM50 subtypes, with enrichment in Luminal B and HER2-enriched tumors. ATP5F1B knockdown reduced proliferation and clonogenic growth, whereas ATP5F1B overexpression enhanced cell growth and was accompanied by decreased BAX and increased BCL-2. Transcriptomic analyses identified ATP5F1B-associated gene expression programs with significant GO/KEGG enrichment. Metabolically, ATP5F1B depletion reduced glycolytic activity and downregulated HK2, PKM2, LDHA, CHPT1, LPCAT1, and ERK-related transcriptional expression.
CONCLUSIONS: ATP5F1B is associated with poor prognosis and promotes breast cancer cell growth, potentially through metabolic regulation.
METHODS: Publicly available breast cancer transcriptomic profiles with matched clinical annotations were analyzed in a family-level screen of mitochondrial ATP synthase subunits. ATP5F1B was prioritized and was evaluated by loss- and gain-of-function assays in AU565 and HCC1428 cells. Differential expression and functional enrichment analyses were performed, and metabolic activity was assessed by extracellular acidification rate. Key genes and proteins were validated by qRT-PCR and Western blotting.
RESULTS: ATP5F1B was upregulated in tumor tissues and emerged as the only screened F1 subunit consistently associated with survival. High ATP5F1B expression was linked to poorer overall survival, disease-specific survival, and progression-free interval, and correlated with clinicopathologic features, including age, estrogen receptor status, and PAM50 subtypes, with enrichment in Luminal B and HER2-enriched tumors. ATP5F1B knockdown reduced proliferation and clonogenic growth, whereas ATP5F1B overexpression enhanced cell growth and was accompanied by decreased BAX and increased BCL-2. Transcriptomic analyses identified ATP5F1B-associated gene expression programs with significant GO/KEGG enrichment. Metabolically, ATP5F1B depletion reduced glycolytic activity and downregulated HK2, PKM2, LDHA, CHPT1, LPCAT1, and ERK-related transcriptional expression.
CONCLUSIONS: ATP5F1B is associated with poor prognosis and promotes breast cancer cell growth, potentially through metabolic regulation.