• ANT1 is overexpressed in colorectal cancer tissues and correlates with poor patient prognosis.
• Knockdown of ANT1 suppresses CRC cell proliferation, migration, and invasion by inhibiting PINK1/Parkin-mediated mitophagy.
• PINK1 overexpression partially rescues the cellular dysfunction caused by ANT1 knockdown, highlighting a potential therapeutic axis.
• In vivo xenograft studies confirm that ANT1 knockdown significantly inhibits tumor growth, suggesting ANT1 as a promising therapeutic target for CRC.
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