7‐amino carboxycoumarin 2 inhibits lactate induced epithelial‐to‐mesenchymal transition via MPC1 in oral and breast cancer cells

• Published in: Cell biology international 2024-08, Vol.48 (8), p.1185-1197
• Main Authors: Umar, Sheikh Mohammad, Dev, Arundhathi J. R., Kashyap, Akanksha, Rathee, Meetu, Chauhan, Shyam S., Sharma, Atul, Prasad, Chandra Prakash
• Format: Article
• Language: English
• Subjects: 7ACC2; AZD3965; Breast cancer; Breast Neoplasms - drug therapy; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cell Line, Tumor; Cell migration; Cell Movement - drug effects; Coumarins - pharmacology; epithelial to mesenchymal transition (EMT); Epithelial-Mesenchymal Transition - drug effects; Female; Glycolysis; Glycolysis - drug effects; Humans; lactate; Lactic acid; Lactic Acid - metabolism; Mitochondrial Membrane Transport Proteins - metabolism; Monocarboxylic Acid Transporters - genetics; Monocarboxylic Acid Transporters - metabolism; Mouth Neoplasms - drug therapy; Mouth Neoplasms - metabolism; Mouth Neoplasms - pathology; MPC1; Oxidative phosphorylation; Oxidative Phosphorylation - drug effects; OXPHOS; Phosphorylation; Pyrimidinones; Symporters - genetics; Symporters - metabolism; Thiophenes; Tumor microenvironment; Tumor Microenvironment - drug effects; Tumors
• ISSN: 1065-6995; 1095-8355; 1095-8355
• DOI: 10.1002/cbin.12172

Lactate is an oncometabolite that play important role in tumor aggressiveness. Lactate from the tumor microenvironment (TME) is taken up by cancer cells as an energy resource via mitochondrial oxidative phosphorylation (or OXPHOS). In the present study, by using an online meta‐analysis tool we demonstrated that in oral squamous cancer cells (OSCCs) glycolytic and OXPHOS governing genes are overexpressed, like in breast cancer. For experimental demonstration, we treated the OSCC cell line (SCC4) and breast cancer cells (MDA‐MB‐231) with sodium L‐lactate and analyzed its effects on changes in EMT and migration. For the therapeutic intervention of lactate metabolism, we used AZD3965 (an MCT1 inhibitor), and 7ACC2 (an MPC inhibitor). Like breast cancer, oral cancer tissues showed increased transcripts of 12 genes that were previously shown to be associated with glycolysis and OXPHOS. We experimentally demonstrated that L‐lactate treatment induced mesenchymal markers and migration of cancer cells, which was significantly neutralized by MPC inhibitor that is, 7ACC2. Such an effect on EMT status was not observed with AZD3965. Furthermore, we showed that lactate treatment increases the MPC1 expression in both cancer cells, and this might be the reason why cancer cells in the high lactate environment are more sensitive to 7ACC2. Overall, our present findings demonstrate that extracellular lactate positively regulates the MPC1 protein expression in cancer cells, thereby putting forward the notion of using 7ACC2 as a potential therapeutic alternative to inhibit malignant oxidative cancers. Future preclinical studies are warranted to validate the present findings.