Key result
Targeting lipid metabolism may overcome acquired resistance to standard breast cancer therapies.
Why the study?
Despite treatment advances, some breast cancer patients develop metastases or recurrence, prompting the need to evaluate how targeting lipid metabolism might improve therapy efficacy.
Targeting lipid metabolism pathways may offer new strategies to overcome drug resistance and improve the efficacy of various breast cancer therapies.
Await prospective data before clinical adoption in resistant breast cancer; leaves open new avenues for reversing therapy resistance.
Breast cancer is the most common malignant tumor in women, and its incidence once surpassed lung cancer in 2020, threatening women’s health. Despite recent advances in the diagnosis and treatment of breast cancer, some patients still develop distant metastases or local recurrence after receiving initial treatment, which leads to a poor prognosis, reduced overall survival, and decreased quality of life. Therefore, finding effective ways to further improve breast cancer outcomes is of great clinical importance. Breast cancer can be categorized into four molecular subtypes based on the expression levels of hormone receptor (HR), human epidermal growth factor receptor 2 (HER2), and Ki-67, and the therapeutic choices vary by molecular type. Disorders of lipid metabolism are among the most prominent metabolic alterations in cancer. In this paper, we will synthesize the roles played by lipid metabolism in different therapeutic treatments for breast cancer, and provide new ideas for using lipid metabolism regulation to improve the efficacy of breast cancer treatment.
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Gong et al. (2026) conducted a review in Breast cancer. Lipid metabolism regulation was evaluated. Targeting lipid metabolism pathways represents a potential therapeutic strategy to overcome acquired resistance to chemotherapy, endocrine therapy, HER2-targeted therapy, and immunotherapy in breast cancer.
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