Role of hydroxymethylglutharyl-coenzyme A reductase in the induction of stem-like states in breast cancer

• Published in: Journal of cancer research and clinical oncology 2024-02, Vol.150 (2), p.106-106, Article 106
• Main Authors: Marks, María Paula, Giménez, Carla Alejandra, Isaja, Luciana, Vera, Mariana Belén, Borzone, Francisco Raúl, Pereyra-Bonnet, Federico, Romorini, Leonardo, Videla-Richardson, Guillermo Agustín, Chasseing, Norma Alejandra, Calvo, Juan Carlos, Vellón, Luciano
• Format: Article
• Language: English
• Subjects: Breast cancer; Breast Neoplasms - pathology; Cancer Research; CD44 antigen; Cell survival; Cholesterol; Coenzyme A; Female; Hematology; Humans; Hydroxymethylglutaryl CoA Reductases - genetics; Hydroxymethylglutaryl CoA Reductases - metabolism; Hydroxymethylglutaryl-CoA reductase; Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology; Internal Medicine; Medicine; Medicine & Public Health; Oncology; Oxidoreductases; Phenotypes; Pluripotency; Statins; Tumor cell lines; Tumors
• ISSN: 1432-1335; 0171-5216; 1432-1335
• DOI: 10.1007/s00432-024-05607-7

Purpose De novo synthesis of cholesterol and its rate-limiting enzyme, 3-hydroxy-3-methylglutharyl-coenzyme A reductase (HMGCR), is deregulated in tumors and critical for tumor cell survival and proliferation. However, the role of HMGCR in the induction and maintenance of stem-like states in tumors remains unclear. Methods A compiled public database from breast cancer (BC) patients was analyzed with the web application SurvExpress. Cell Miner was used for the analysis of HMGCR expression and statin sensitivity of the NCI-60 cell lines panel. A CRISPRon system was used to induce HMGCR overexpression in the luminal BC cell line MCF-7 and a lentiviral pLM-OSKM system for the reprogramming of MCF-7 cells. Comparisons were performed by two-tailed unpaired t-test for two groups and one- or two-way ANOVA. Results Data from BC patients showed that high expression of several members of the cholesterol synthesis pathway were associated with lower recurrence-free survival, particularly in hormone-receptor-positive BC. In silico and in vitro analysis showed that HMGCR is expressed in several BC cancer cell lines, which exhibit a subtype-dependent response to statins in silico and in vitro. A stem-like phenotype was demonstrated upon HMGCR expression in MCF-7 cells, characterized by expression of the pluripotency markers NANOG, SOX2, increased CD44 +/CD24low/ −, CD133 + populations, and increased mammosphere formation ability. Pluripotent and cancer stem cell lines showed high expression of HMGCR, whereas cell reprogramming of MCF-7 cells did not increase HMGCR expression. Conclusion HMGCR induces a stem-like phenotype in BC cells of epithelial nature, thus affecting tumor initiation, progression and statin sensitivity.