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Taken together, these studies underscore the therapeutic potential of iPSC-derived neural progenitors in PD models, yet the variability in reprogramming methods reported in the aforementioned studies, limited scalability, and unresolved concerns around long-term safety and functional integration highlight the need for more standardized and clinically validated approaches

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This regulatory network is mainly manifested by abnormal hypermethylation of CpG islands in the promoter region, leading to transcriptional silencing of important tumor suppressor genes such as PTEN, RASSF1A, p16 (CDKN2A), and hMLH1