Collective cell migration is fundamental to gaining insights into various important biological processes such as wound healing and cancer metastasis. In particular, recent in vitro studies and in silico simulations suggest that mechanics can explain the social behavior of multicellular clusters to a large extent with minimal knowledge of various cellular signaling pathways. These results suggest that a mechanistic perspective is necessary for a comprehensive and holistic understanding of collective cell migration, and this review aims to provide a broad overview of such a perspective. Cell migration plays a pivotal role in regulating numerous biological processes under both physiological as well as pathological conditions. Single cells need to interact with their environment to move. This is done by employing a number of different cellular structures such as lamellipodia, filopodia, and podosomes. Although the typical steps involved in the migration of an individual cell over a substrate have already been well studied and characterized (57, 58) (FIGURE 1A), recent advances in imaging and molecular biology techniques have enabled us to better probe and visualize these events. Experimental and theoretical analyses strongly suggest that the migratory behavior of single cells in the absence of any external physical or chemical stimuli can be well described by a persistent random walk model (25). Spontaneous lamellipodium formation can randomly polarize a cell and allow them to migrate in a specific direction. Since the persistence of migration under such conditions is very low, they are able to migrate only short distances. However, for cells to be functional in several processes, they need to be able to migrate persistently in a specific direction over long distances. Breaking this "symmetry" (i.e., equal probability to migrate in all directions) requires either external chemical gradients from soluble (chemotaxis) and substrate-bound [haptotaxis (19, 20, 37)] ligands or physical (30) cues within the extracellular environment that introduce a bias such that cells are forced to prefer a particular direction to migrate. For example, leukocytes are strongly attracted to inflammatory chemokines secreted by various cells. The role of chemical cues in guiding and regulating cell migration has been extensively studied and still remains a topic of intense research. However, the role of mechanical and physical cues within the cellular microenvironment in governing cell migration has only recently garnered much attention (35,70).The application of microfabrication and soft lithography techniques have further boosted our ability to better interrogate the role of micromechanical cues in regulating cell migration (36,63).However, it is well recognized that, in several biological processes [e.g., gastrulation (32, 75), wound healing (40) and cancer metastasis (22)], cells do not migrate individually but rather collectively either as clusters, chains, or sheets. Collective migration serves to keep the tissue intact during remodel...