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This  system  demonstrated  remarkable  tumor-suppressive  efficacy,  anti-metastatic

                   activity, and pro-regenerative properties in post-surgical applications. Building on this

                   concept,  Li  et  al.   110   developed  a  fish  gelatin  (F-Gel)/berberine  (BBR)  composite
                   scaffold for post-operative gastric cancer therapy, which exhibited potent tumor growth

                   inhibition and excellent biocompatibility, further validating the potential of hybrid 3D-

                   printed microfluidic scaffolds in precision oncology and regenerative medicine. These

                   advances highlight the transformative role of convergent biofabrication technologies in

                   creating multifunctional implants for cancer therapy and tissue repair.

                       While  integrated  3D-microfluidic  bioprinting  platforms  have  revolutionized

                   preclinical drug development and therapeutic delivery, their clinical impact extends

                   beyond  treatment  to  transformative  diagnostic  capabilities.  The  same  engineering

                   principles  enabling  physiologically  relevant  tumor  models  and  targeted

                   nanotherapeutics—precision  fluidic  control,  biomimetic  spatial  design,  and  patient-

                   specific  customization—now  empower  the  development  of  next-generation  liquid

                   biopsy  platforms.  By  transitioning  focus  from  therapeutic  intervention  to  early

                   detection and real-time monitoring, these technologies address a critical unmet need in
                   oncology:  minimally  invasive,  longitudinal  tracking  of  tumor  dynamics  to  guide

                   precision therapy adjustments.



                   5.  3D-Printed  Microfluidic  Platforms  for  Cancer  Diagnostics  and  Biomarker

                   Detection

                        While tissue biopsy remains the clinical gold standard for tumor characterization,

                   its invasiveness limits serial disease monitoring, especially when sample volumes are

                   insufficient  for  diverse  molecular  testing   111 .  Liquid  biopsy  approaches  analyzing

                   circulating  tumor-derived  components—including  circulating  tumor  cells  (CTCs),

                   circulating  tumor  DNA  (ctDNA),  exosomes,  and  proteomic  signatures—provide

                   minimally  invasive  access  to  real-time  tumor  dynamics   112,113 .  State-of-the-art  3D-

                   printed  microfluidic  systems  have  achieved  unprecedented  precision  in  tumor

                   biomarker isolation through bioinspired architectures that recapitulate key features of


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