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Related Concept Videos

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Cancer Stem Cells and Tumor Maintenance

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Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
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Targeted Cancer Therapies02:57

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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Updated: Aug 24, 2025

A Spheroid Killing Assay by CAR T Cells
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CAR cell design strategies in solid tumors.

Lu Wang1, Xinyi Chen1, Lu Zhang1

  • 1Department of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jie Fang Road 1095, Wuhan, Hubei, China.

International Immunopharmacology
|October 22, 2022
PubMed
Summary

Chimeric antigen receptor (CAR) cell therapies, including CAR-NK, CAR-NKT, CAR-M, and CAR-γδ T-cells, show promise for solid tumors. Overcoming challenges like tumor heterogeneity is key for effective CAR cell therapy development.

Keywords:
Chimeric antigen receptorCytokine release syndromeDesign strategySolid tumors

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3D Cell-Printed Hypoxic Cancer-on-a-Chip for Recapitulating Pathologic Progression of Solid Cancer
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Area of Science:

  • Immunology
  • Oncology
  • Biotechnology

Background:

  • Chimeric antigen receptor (CAR) cell therapy is expanding beyond CAR-αβ T-cells to include CAR-NK, CAR-NKT, CAR-M, and CAR-γδ T-cells for solid tumor treatment.
  • Solid tumors present unique challenges including heterogeneity, limited antigen targets, and an immunosuppressive microenvironment, hindering CAR cell therapy efficacy compared to hematological malignancies.

Purpose of the Study:

  • To analyze the application of various CAR cell types in solid tumors.
  • To summarize design principles for CAR cell therapies targeting solid tumors.
  • To guide future development of CAR cell therapy for solid tumors.

Main Methods:

  • Comprehensive review of existing literature on CAR cell therapy in solid tumors.
  • Analysis of the characteristics of solid tumors that impact CAR cell efficacy.
  • Examination of design strategies for different CAR cell modalities.

Main Results:

  • Different CAR cell types (NK, NKT, M, γδ T) are being explored for solid tumors.
  • Solid tumor characteristics pose significant obstacles to CAR cell therapy effectiveness.
  • Specific design principles are emerging for optimizing CAR cells against solid tumors.

Conclusions:

  • CAR cell therapy holds potential for solid tumors, but challenges must be addressed.
  • Tailoring CAR cell design to tumor-specific features is crucial.
  • Further research into CAR cell engineering is needed to improve solid tumor treatment outcomes.