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Soman and Vijayavenkataraman
           mimic the tumor microenvironment (TME). The         of establishing a cancer iPSC depends on the type
           commonly used cancer bioprinting methods are:       cancer. So far, the  successful  reprogramming of
           Inkject  printing, extrusion-based printing,  lase-  myeloid tumors is established [137-139] . Establishing
           assisted printing, and SLA. The tissues can be 3D   protocols for generating  cancer iPSCs can help
           bioprinted in the format of spheroids, organoids,   to model cancer progression, to understand the
           coculture with other tumor TME cells, and organ-    complex  cancer  genetics,  and contribution  of
           on chip. Improvements in the 3D bioprinting         TME in cancer progression, anti-cancer  drug
           technology  enable  to distribute  the  cancer      development, and precision oncology (Figure 4).
           derived iPSCs in a 3D space with high precision
           and reproducibility.  The 3D bioprinted  tissues    4.4 Bioprinted iPSCs for drug and cosmetic
           can be used as cancer  tissue-on-chip  models  or   testing
           transplanted into animal models to study different   4.4.1 Bioprinted iPSCs for drug testing
           stages of cancer pathogenesis.
             The  most important  hurdle  in  establishing     More than 90% of drug molecules under different
           iPSC-derived cancer models are the variation of     phase of clinical trials fail to reach market because
           intrinsic transcription factors in the cancer cells.   of unanticipated toxicity to vital organs or lack of
           This  variation  can  affect  the  reprogramming    efficacy.  This  failure  rate  is  partly  attributed  to
           efficiency of tumor cells. Many published studies   the use of overly simplistic 2D cell culture-based
           showed that cancer cells are generally difficult to   assays [140] .  The spectrum  of activity  of most of
           reprogram than normal cells [136] . The differentiation   the drug molecules varied across the species, so
           of cancer iPSCs to its initial tumor cell of origin also   animal testing has limited predictive value [107] . 3D
           appears tedious and inconsistent. The success rate   bioprinting and iPSC technology enable printing of





































           Figure 4. Bioprinted cancer tissue with induced pluripotent stem cell (iPSC)-derived cells: Establishing
           protocols for generating cancer iPSCs can help to model cancer progression, to understand the complex
           cancer genetics, and contribution of tumor microenvironment in cancer progression, anti-cancer drug
           development, and precision oncology.

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