Sphingomyelin synthase 2 promotes an aggressive breast cancer phenotype by disrupting the homoeostasis of ceramide and sphingomyelin

• DOI: 10.1038/s41419-019-1303-0
• Publication Date: 2019-02-15T11:03:55Z
• Authors: Kehong Zheng; Zetao Chen; Haizhan Feng; Ying Chen; Cheng Zhang; Jinlong Yu; Yunfeng Luo; Liang Zhao; Xiancheng Jiang; Fujun Shi
• Keywords: Male; Mice, Inbred BALB C; 0303 health sciences; Epithelial-Mesenchymal Transition; Carcinoma, Ductal, Breast; Membrane Proteins; Mice, Nude; Breast Neoplasms; Nerve Tissue Proteins; Ceramides; Article; 3. Good health; Mice; 03 medical and health sciences; Phenotype; Cell Movement; MCF-7 Cells; Animals; Heterografts; Homeostasis; Humans; Female; RNA, Small Interfering; Cell Proliferation

AbstractBreast cancer is the most common type of carcinoma in women worldwide, but the mechanisms underlying tumour development and progression remain unclear. Sphingomyelin synthase 2 (SGMS2) is a crucial regulator involved in ceramide (Cer) and sphingomyelin (SM) homoeostasis that is mostly studied for its role in lipid metabolism. Our primary study indicated that high SGMS2 expression is associated with breast cancer metastasis. Gain- and loss-of-function assays in vitro and in vivo revealed that SGMS2 promotes cancer cell proliferation by suppressing apoptosis through a Cer-associated pathway and promotes cancer cell invasiveness by enhancing epithelial-to-mesenchymal transition (EMT) initiation through the TGF-β/Smad signalling pathway. Further study determined that SGMS2 activated the TGF-β/Smad signalling pathway primarily by increasing TGF-β1 secretion, which was likely associated with aberrant expression of SM. Thus, our findings indicate that SGMS2-mediated activation of the TGF-β/Smad signalling pathway is important in breast cancer progression, which provides new insight into the mechanisms underlying breast cancer metastasis and suggests a possible anticancer therapy for breast cancer.