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The Tumor Microenvironment02:17

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Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
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Bioprinting the Cancer Microenvironment.

Yu Shrike Zhang1, Margaux Duchamp2, Rahmi Oklu3

  • 1Biomaterials Innovation Research Center, Division of Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 65 Landsdowne Street, Cambridge, Massachusetts 02139, United States; Harvard-MIT Division of Health Sciences and Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States; Wyss Institute for Biologically Inspired Engineering, Harvard University, 3 Blackfan Circle, Boston, Massachusetts 02115, United States.

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Summary

Bioprinting creates advanced 3D cancer models that better mimic tumor complexity and microenvironments. These biomimetic models improve cancer research, drug screening, and understanding of cancer development and metastasis.

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bioprintingcancer biologycancer modeldrug screeningvascularization

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Area of Science:

  • Oncology
  • Biofabrication
  • Biomedical Engineering

Background:

  • Cancer involves complex cellular and microenvironmental interactions crucial for progression.
  • Traditional 2D and 3D cancer models lack vascularization and fail to replicate tumor complexity.
  • Limitations hinder their use in drug screening and fundamental cancer biology research.

Purpose of the Study:

  • To review bioprinting strategies for creating advanced cancer models.
  • To highlight the role of bioprinting in mimicking the tumor microenvironment.
  • To discuss the application of bioprinting in cancer research and drug development.

Main Methods:

  • Review of current literature on bioprinting techniques for cancer modeling.
  • Analysis of bioink selection for replicating tumor matrix properties.
  • Discussion of methods for bioprinting vascular structures within cancer models.

Main Results:

  • Bioprinting enables high-resolution 3D structure creation for biomimetic cancer models.
  • Advanced models accurately recreate cancer microenvironment complexity, including vascularization.
  • Bioprinted models show promise for studying cancer genesis, metastasis, and drug responses.

Conclusions:

  • Bioprinting offers a versatile platform for developing sophisticated cancer models.
  • These models overcome limitations of conventional approaches, enhancing cancer research applications.
  • Future perspectives focus on further refining bioprinted cancer models for clinical relevance.