Cancer survivorship programs in India for Global Patients
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Read MoreGene therapy for cancer marks a new era in treatment, using advanced methods to target cancer at the genetic level for better and focused outcomes.
Category
CancerPublished By
GetWellGo TeamUpdated on
07-Apr-2025Cancer gene therapy refers to deriving a method of treatment whereby genes are altered in cancer cells or immune cells in the body that have a role of combating cancer cells. It is still considered to be rather new and some of them are still in experimental stage while others have received approval.
Gene Addition Therapy
Gene Editing (CRISPR/Cas9 and Other Technologies)
Suicide Gene Therapy
Immunogene Therapy or also known as Genetically Engineered Immune Cells.
Oncolytic Virus Therapy
Application of gene therapy has emerged as relevant tool for cancer treatment with lung cancer, specifically NSCLC being considered as a suitable candidate for this treatment. It involves altering of genes in carcinogenic cells or immune cells in a way that inhibits cell growth of tumor or improves immune activity against cancerous cells or makes the cancerous cells to be more susceptible to treatment.
Tumor-Suppressor Gene Therapy
Suicide Gene Therapy
Oncolytic Virus Therapy
CAR-T Cell Therapy for Lung Cancer
RNA-Based Gene Therapy
Gene therapy is considered as a possible cure for breast cancer, especially in cases with aggressive or non-responsive to treatment cycles like TNBC and HER2-positive BC. It is to either fix defective genes, boost the ability of the immune system or to make cancer cells more vulnerable to medications.
CRISPR or Clustered Regularly Interspaced Short Palindromic Repeats is the revolutionary technique for editing the genes of an organism. In cancer therapy, CRISPR enhances the genes of cancer cells or immune cells to influence cancer therapy.
Gene editing is revolutionizing cancer immunotherapy by modifying immune cells to more effectively see and kill cancer. Technologies such as CRISPR, TALEN, and Zinc Finger Nucleases (ZFNs) enable precise immune cell modifications to improve their anti-tumor function.
Types of Gene Editing in Immunotherapy
CRISPR-Edited CAR-T Cell Therapy
Purpose: Improves Chimeric Antigen Receptor (CAR)-T cells to better attack cancer cells.
TCR-T Cell Therapy (T Cell Receptor Therapy)
Purpose: Strengthens T cells by editing their T cell receptors (TCRs) to recognize cancer antigens more effectively.
CRISPR for Checkpoint Inhibitor Therapy
Purpose: Enhances immune checkpoint blockade therapy (e.g., PD-1/PD-L1 inhibitors).
Gene-Edited NK Cell Therapy (Natural Killer Cells)
Purpose: Strengthens NK cells, a category of immune cell that naturally destroys cancer.
Dendritic Cell Therapy with Gene Editing
Purpose: Spreads antigen-presenting dendritic cells (DCs) to enhance immune response.
Personalized gene therapy for cancer is making treatments tailored according to a patient's genetic profile and tumor's molecular attributes. This will enhance the efficiency of treatment, decrease side effects, and achieve overcoming drug resistance.
Assists in determining the most potent drugs according to the genetic mutations in the tumor.
Gene therapy is a promising method of cancer treatment, but it also has possible risks and side effects. These side effects may differ based on the type of gene therapy, delivery method, and patient response.
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