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Updated: Feb 1, 2026

Studying the Role of Alveolar Macrophages in Breast Cancer Metastasis
Published on: June 26, 2016
Inhibition of breast cancer metastasis to the lungs with UBS109
Mamoru Shoji1, Wei Ping Qian2, Ganji Purnachandra Nagaraju1
1Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
Abstract:
Synthetic monocarbonyl analogs of curcumin (MACs) are cytotoxic against several cancers including head and neck cancer, pancreatic cancer, colon cancer, and breast cancer. Mechanisms of action include depolarization of the mitochondrial membrane potential and inhibition of NF-κB, leading to apoptosis. We previously demonstrated that UBS109 (MAC), has preventive effects on bone loss induced by breast cancer cell lines. We determined whether UBS109 could inhibit and prevent lung metastasis, since lung metastasis of breast cancer is a major problem in addition to bone metastasis. A breast cancer lung metastasis (colonization) model was created by injection of breast cancer cells MDA-MB-231 into the tail vein of athymic nude mice, nu/nu. Animals were treated with vehicle or UBS109 at 5 or 15 mg/kg body weight by intraperitoneal injection once daily 5 days a week for 5 weeks. UBS109 at 15 mg/kg significantly inhibited lung metastasis/colonization as demonstrated by reduced lung weight consisting of tumor nodules. The body weight of animals treated with UBS109 15 mg/kg remained the same as in the other groups. UBS109 killed completely (100%) MDA-MB-231 breast cancer cells at 1.25 μM in a cytotoxicity assay in vitro. UBS109 15 mg/kg i.p. showed a maximal blood concentration (Cmax) of 432 ± 387 ng/mL at 15 min post injection. This is approximately 1.5 ng/ml in the blood of mice and equals 1.5 μM of UBS109. These in vitro and in vivo results are consistent with each other.
Insights
Synthetic monocarbonyl analogs of curcumin (MACs) show promise in cancer treatment. UBS109, a MAC, significantly inhibited breast cancer lung metastasis in mice, demonstrating its potential as an anti-cancer therapeutic.
Area of Science:
- Pharmacology and Toxicology
- Oncology
- Cancer Metastasis Research
Background:
- Synthetic monocarbonyl analogs of curcumin (MACs) exhibit cytotoxicity against various cancers.
- Previous studies showed UBS109 (a MAC) prevents bone loss induced by breast cancer.
- Lung metastasis is a significant challenge in breast cancer treatment.
Purpose of the Study:
- To investigate the efficacy of UBS109 in inhibiting and preventing lung metastasis of breast cancer.
- To evaluate the anti-cancer activity of UBS109 in a preclinical lung metastasis model.
Main Methods:
- A breast cancer lung metastasis model was established using MDA-MB-231 cells injected into athymic nude mice.
- Mice were treated with UBS109 (5 or 15 mg/kg) or vehicle via intraperitoneal injection for 5 weeks.
- Cytotoxicity assays were performed in vitro, and pharmacokinetic analysis (Cmax) was conducted in vivo.
Main Results:
- UBS109 at 15 mg/kg significantly reduced lung metastasis, indicated by decreased lung weight and tumor nodules.
- UBS109 demonstrated complete eradication (100%) of MDA-MB-231 cells at 1.25 μM in vitro.
- Pharmacokinetic studies showed a Cmax of 432 ± 387 ng/mL at 15 min post-injection for UBS109 (15 mg/kg i.p.).
Conclusions:
- UBS109 effectively inhibits and prevents breast cancer lung metastasis in a preclinical mouse model.
- The in vitro and in vivo findings support UBS109's anti-metastatic and cytotoxic potential against breast cancer.
- UBS109 represents a promising therapeutic agent for managing breast cancer metastasis.
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