MMP-3 cleavage of Lamin A induces pro-migratory nuclear deformity, nucleophagy, and their autophagic secretion with extracellular vesicles in metastatic cancer

Matrix metalloproteinases (MMPs) are a family of zinc-dependent proteinases that cleave a plethora of substrates, including components of the extracellular matrix and cell-surface-associated proteins, as well as intracellular targets. MMPs have also been found in extracellular vesicles (EVs), such as exosomes. MMP-3 promotes tumor growth, epithelial-to-mesenchymal transition, genome instability, migration, invasion, and metastasis of cancer cells, and nuclear MMP-3 controls gene transcription. Intranuclear proteolysis by MMPs may significantly alter cancer progression. However, the nuclear substrates of MMP-3 have not been well investigated. In this study, we performed proteomic analyses to identify the nuclear substrates and EV proteins regulated by MMP-3. While rabidly metastatic colon cancer (LuM1) three-dimensionally cultured tumoroids secreted EVs containing 30 protein types, including Lamin A (LMNA), MMP-3, fibronectin (FN1), HSPA8 (Hsc70), β-actin (ACTB), and vimentin (VIM), CRISPR/Cas9-based knockout of MMP-3 reduced the secretion of these proteins in EVs. Notably, EV-bound cleaved Lamin secretion was confirmed by immunoelectron microscopy. Also, MMP-3 formed proteolytic dimers via its hemopexin-like repeat domains in nuclei. Many nuclear MMP-3-binding proteins, including Lamin A/C, histones, topoisomerases, and hnRNPs, were screened by co-immunoprecipitation followed by proteomics. Proteolytic MMP-3 overexpression generated a C-terminal 30-kDa fragment of Lamin A, whose cleavage site was defined via structural analysis. MMP-3 digestion of Lamin A induced nuclear deformity (atypia) required for cell migration in confined space. The cleaved Lamin A and MMP-3 were transported with autophagosomes (LC3B+), nucleophagosomes, and amphisomes (CD63 + LC3B+) and co-secreted with EVs. Proteolytic MMP-3 also induced nuclear speckles of Lamin A, suggesting their roles in transcription and splicing. Clinical analysis revealed that high expressions of MMP3 and LMNA were significantly seen in head and neck squamous cell carcinoma (HNSC) than in the other 16 cancer types, and predicted poor prognosis of patients suffering from HNSC, pancreatic, rectum and lung adenocarcinomas at specific stages. Immunohistochemistry revealed that nuclear MMP-3 and cleaved Lamin were significantly higher expressed in stage IV metastatic HNSC cases than in stage I non-metastatic cases. Taken together, MMP3-cleavage of Lamin A induces nuclear deformity, nucleophagy, and their autophagic co-secretion with EVs in metastatic cancer. Also, high expression of MMP-3 and secretion of Lamin A can predict poor prognosis in multiple cancer types at specific stages. Matrix metalloproteinases (MMPs) are a family of zinc-dependent proteinases that cleave a wide range of substrates, including components of the extracellular matrix and cell-surface-associated proteins, as well as intracellular targets. MMP-3 promotes tumor growth, migration, invasion, and metastasis of cancer cells, and nuclear MMP-3 controls gene transcription. Here, we performed proteomic analyses to identify the nuclear substrates and extracellular vesicle (EV)-bound proteins regulated by MMP-3. While three-dimensionally cultured, rabidly metastatic colon cancer tumoroids secreted EVs containing 30 protein types, including Lamin A (LMNA), MMP-3, and vimentin (VIM), knockout of MMP-3 reduced the secretion of these proteins in EVs. EV-bound cleaved Lamin secretion was confirmed by immunoelectron microscopy. Nuclear MMP-3 formed proteolytic dimers via its PEX domains. Many nuclear MMP-3-binding proteins, including LMNA, were screened by proteomics. MMP-3 overexpression generated a C-terminal 30-kDa fragment of LMNA, whose cleavage site was defined via structural analysis. MMP-3 digestion of Lamin A induced nuclear deformity required for cell migration in confined space. The cleaved LMNA and MMP-3 were co-transported via autophagosomes and amphisomes and co-secreted with EVs. MMP-3 also induced LMNA nuclear speckles. Clinically, high expressions of MMP3 and LMNA were seen in head and neck squamous cell carcinoma (HNSC) than in the other 16 cancer types, and predicted poor prognosis in HNSC, pancreatic, rectum and lung adenocarcinomas at specific stages. Nuclear MMP-3 and cleaved Lamin were significantly higher expressed in metastatic HNSC cases than in non-metastatic cases. Taken together, MMP3-cleavage of Lamin A induces nuclear deformity and their autophagic co-secretion with EVs in metastatic cancer. Also, high expression of MMP-3 and secretion of Lamin A can predict poor prognosis in multiple cancer types at specific stages.