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Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

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Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
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Mitogens and the Cell Cycle02:38

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Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
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Adaptive Mechanisms in Cancer Cells02:53

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Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
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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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Cancer Stem Cells and Tumor Maintenance02:40

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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.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
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Related Experiment Video

Updated: Jul 9, 2025

Generation of Induced Pluripotent Stem Cells from Human Melanoma Tumor-infiltrating Lymphocytes
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Reprogramming endothelial cells to empower cancer immunotherapy.

Abigail H Cleveland1, Yi Fan1

  • 1Department of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, USA.

Trends in Molecular Medicine
|December 1, 2023
PubMed
Summary

The tumor vasculature actively suppresses anti-cancer immunity and immunotherapy response through various mechanisms. Reprogramming endothelial cells offers a novel strategy to overcome this resistance and enhance cancer treatment.

Keywords:
CAR T cellsangiogenesiscancer immunotherapyendothelial cell metabolismtumor microenvironmentvascular reprogramming

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Area of Science:

  • Oncology
  • Immunology
  • Vascular Biology

Background:

  • Tumor immunity is regulated by leukocyte interactions within the tumor microenvironment.
  • The tumor vasculature plays a critical role in immune evasion and immunotherapy resistance.
  • Conventional roles of tumor vasculature include nutrient and oxygen supply.

Purpose of the Study:

  • To elucidate multiplex mechanisms by which tumor vasculature regulates anti-cancer immunity.
  • To explore the potential of targeting endothelial cells for overcoming immunotherapy resistance.

Main Methods:

  • Review and synthesis of current evidence on vascular regulation of tumor immunity.
  • Postulation of mechanisms involving angiocrine education, endothelial metabolism, and vascular architecture.
  • Hypothesizing genetic and metabolic reprogramming of endothelial cells.

Main Results:

  • The tumor vasculature creates an immunosuppressive niche via angiocrine factors.
  • Aberrant endothelial metabolism leads to T cell exclusion and inactivation.
  • Abnormal vascular topology and biochemistry impede lymphocyte infiltration.

Conclusions:

  • The tumor vasculature actively suppresses anti-cancer immunity and immunotherapy.
  • Targeting endothelial cell reprogramming presents a promising next-generation strategy for cancer therapy.
  • Reprogramming endothelial cells can overcome immunotherapy resistance by modulating the tumor microenvironment.