Epidermal growth factor receptor (EGFR) plays a pivotal role in collective cell migration by mediating cell-to-cell propagation of extracellular signal-regulated kinase (ERK) activation. Here, we aimed to determine which EGFR ligands mediate the ERK activation waves. We found that epidermal growth factor (<italic>EGF</italic>)–deficient cells exhibited lower basal ERK activity than the cells deficient in heparin-binding EGF (<italic>HBEGF</italic>), transforming growth factor alpha (<italic>TGFα</italic>) or epiregulin (<italic>EREG</italic>), but all cell lines deficient in a single EGFR ligand retained the ERK activation waves. Surprisingly, ERK activation waves were markedly suppressed, albeit incompletely, only when all four EGFR ligands were knocked out. Re-expression of the EGFR ligands revealed that all but HBEGF could restore the ERK activation waves. Aiming at complete elimination of the ERK activation waves, we further attempted to knockout <italic>NRG1</italic>, a ligand for ErbB3 and ErbB4, and found that <italic>NRG1</italic>-deficiency induced growth arrest in the absence of all four EGFR ligand genes. Collectively, these results showed that EGFR ligands exhibit remarkable redundancy in the propagation of ERK activation waves during collective cell migration.