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<p>Triple-negative breast cancer (TNBC) is characterized by extensive metabolic alterations that enable its sustained growth therapeutic resistance. Nicotinamide phosphoribyltransferase (NAMPT) catalyzes the first and rate-limiting step in the nicotinamide dinucleotide (NAD) salvage pathway. Elevated NAMPT is associated with increased aggressiveness and poor prognosis in multiple cancers. Previously, we showed the role of TRAF3IP2 in TNBC tumorigenesis. Here, we aim to show that the anti-tumorigenic effects resulting from TRAF3IP2 inhibition are driven in part by decreases in cellular energetics in TNBC cells. Results show that inhibition of TRAF3IP2 leads to significant decrease in NAMPT expression, reduced NAD and ATP production, and disruption of TNBC bioenergetics through cell line-specific alterations in glycolysis and mitochondrial function. Notably, the established MDA-MB-231 line and the patient-derived 4IC model exhibited distinct OCR responses, underscoring metabolic heterogeneity across TNBC models. Additionally, this study showed that targeting TRAF3IP2 disrupts cellular energetics by affecting AMPK/LKB1 and mTOR signaling pathways and increasing reactive oxygen species (ROS) levels, ultimately leading to reduced cell viability and increased apoptosis. These findings suggest that TRAF3IP2 plays a critical role in maintaining TNBC bioenergetics and represents a potential target for therapeutic intervention.</p>

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Targeting TRAF3IP2 disrupts cellular energetics through inhibition of NAMPT in triple negative breast cancer

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年12月23日

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  • Kurtis Willingham,
  • Amin Izadpanah,
  • Yasmine Rashad,
  • Antonia Reilich,
  • Fatemeh Daneshimehr,
  • Steven Braun,
  • Eckhard U. Alt,
  • Reza Izadpanah

摘要

Triple-negative breast cancer (TNBC) is characterized by extensive metabolic alterations that enable its sustained growth therapeutic resistance. Nicotinamide phosphoribyltransferase (NAMPT) catalyzes the first and rate-limiting step in the nicotinamide dinucleotide (NAD) salvage pathway. Elevated NAMPT is associated with increased aggressiveness and poor prognosis in multiple cancers. Previously, we showed the role of TRAF3IP2 in TNBC tumorigenesis. Here, we aim to show that the anti-tumorigenic effects resulting from TRAF3IP2 inhibition are driven in part by decreases in cellular energetics in TNBC cells. Results show that inhibition of TRAF3IP2 leads to significant decrease in NAMPT expression, reduced NAD and ATP production, and disruption of TNBC bioenergetics through cell line-specific alterations in glycolysis and mitochondrial function. Notably, the established MDA-MB-231 line and the patient-derived 4IC model exhibited distinct OCR responses, underscoring metabolic heterogeneity across TNBC models. Additionally, this study showed that targeting TRAF3IP2 disrupts cellular energetics by affecting AMPK/LKB1 and mTOR signaling pathways and increasing reactive oxygen species (ROS) levels, ultimately leading to reduced cell viability and increased apoptosis. These findings suggest that TRAF3IP2 plays a critical role in maintaining TNBC bioenergetics and represents a potential target for therapeutic intervention.