“…However, as mentioned previously, the canonical 2D culture and differentiation of these cells still has major limitations, most notably their immature phenotype, which lacks to fully represent developed tissue. The development of new biomaterials (Reis et al, 2016;Wissing et al, 2017;Kuraitis et al, 2019) and the emerging of new technologies such as tissue printing (Charbe et al, 2019;Tomov et al, 2019), organ on a chip (Marsano et al, 2016;Ugolini et al, 2018;Wan et al, 2018), and different types of bioreactors that allow mechanical, perfusion, or electrical stimulation (Freed et al, 2006;Lei and Ferdous, 2016;Paez-Mayorga et al, 2019) allow us to generate cardiac tissue that more closely recapitulate the (patho)physiological features of the developed myocardium. Moreover, these models represent an optimal tool not only to test and validate new drugs or to re-create tissue substitute for regenerative medicine application but also to allow a better understanding of the molecular mechanisms behind disease development and progression.…”