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Updated: Feb 7, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Disrupting cholesterol esterification by bitter melon suppresses triple-negative breast cancer cell growth
So Hee Shim1, Subhayan Sur1, Robert Steele1
1Departments of Pathology, Saint Louis University, St. Louis, Missouri.
Abstract:
Triple negative breast cancer (TNBC) is aggressive with a worse prognosis. We have recently shown that bitter melon extract (BME) treatment was more effective in inhibition of TNBC tumor growth in mouse models as compared to ER positive breast tumor growth. Aberrant dysregulation of lipid metabolism is associated with breast cancer progression, however, anti-cancer mechanism of BME linking lipid metabolism in breast cancer growth remains unexplored. Here, we observed that accumulation of esterified cholesterol was reduced in BME treated TNBC cell lines as compared to control cells. We next evaluated expression levels of acyl-CoA: cholesterol acyltransferase 1 (ACAT-1) in TNBC cells treated with BME. Our results demonstrated that BME treatment inhibited ACAT-1 expression in TNBC cells. Subsequently, we found that sterol regulatory element-binding proteins-1 and -2, and FASN was significantly reduced in BME treated TNBC cell lines. Low-density lipoprotein receptor was also downregulated in BME treated TNBC cells as compared to control cells. We further demonstrated that BME feeding reduced tumor growth in TNBC mammospheres implanted into NSG mice, and inhibits ACAT-1 expression. To our knowledge, this is the first report demonstrating BME suppresses TNBC cell growth through ACAT-1 inhibition, and have potential for additional therapeutic regimen against human breast cancer.
Insights
Bitter melon extract (BME) effectively inhibits aggressive triple-negative breast cancer (TNBC) growth by targeting lipid metabolism. BME suppresses acyl-CoA: cholesterol acyltransferase 1 (ACAT-1) expression, offering a potential new therapy for TNBC.
Area of Science:
- Oncology
- Metabolic Research
- Natural Product Therapeutics
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype with limited therapeutic options.
- Dysregulated lipid metabolism is increasingly recognized as a driver of breast cancer progression.
- The anti-cancer mechanisms of bitter melon extract (BME) concerning lipid metabolism in TNBC remain largely unexplored.
Purpose of the Study:
- To investigate the anti-cancer effects of BME on TNBC.
- To elucidate the role of lipid metabolism, specifically acyl-CoA: cholesterol acyltransferase 1 (ACAT-1), in BME's mechanism of action against TNBC.
Main Methods:
- Treatment of TNBC cell lines and mouse models with BME.
- Analysis of esterified cholesterol accumulation, ACAT-1 expression, and key lipid metabolism regulators (SREBPs, FASN, LDLR).
- In vivo studies using TNBC mammospheres implanted into NSG mice.
Main Results:
- BME treatment reduced esterified cholesterol accumulation in TNBC cells.
- BME significantly inhibited ACAT-1 expression in TNBC cells.
- BME downregulated SREBP-1, SREBP-2, FASN, and LDLR expression, and suppressed tumor growth in vivo.
Conclusions:
- This study demonstrates that BME suppresses TNBC cell growth.
- BME's anti-cancer effect is mediated through the inhibition of ACAT-1 and associated lipid metabolic pathways.
- BME shows potential as an adjunct therapeutic agent for human breast cancer.
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