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Related Concept Videos

The Tumor Microenvironment02:17

The Tumor Microenvironment

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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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Related Experiment Video

Updated: Mar 2, 2026

Quantification of Tumor Cell Adhesion in Lymph Node Cryosections
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Quantification of Tumor Cell Adhesion in Lymph Node Cryosections

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Lymph node effective vascular permeability and chemotherapy uptake.

Eelco F J Meijer1,2, Cedric Blatter2,3, Ivy X Chen1,2

  • 1Edwin L. Steele Laboratories for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital Cancer Center, Boston, MA, USA.

Microcirculation (New York, N.Y. : 1994)
|May 17, 2017
PubMed
Summary
This summary is machine-generated.

Vascular permeability in lymph nodes can be increased by vascular endothelial growth factor-A (VEGF-A). However, this did not improve chemotherapy drug penetration into lymph node metastases.

Keywords:
chemotherapydrug penetrationintravital microscopylymph nodevascular permeability

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Area of Science:

  • Oncology
  • Vascular Biology
  • Pharmacology

Background:

  • Lymph node metastases are a significant prognostic factor in cancer.
  • Therapeutic responses in lymph node metastases can differ from primary tumors.
  • Understanding lymph node vasculature is crucial for optimizing systemic drug delivery.

Purpose of the Study:

  • To measure effective vascular permeability in lymph node blood vessels.
  • To investigate if increasing vascular permeability enhances chemotherapy penetration into lymph nodes.

Main Methods:

  • Developed a novel 3D method to measure in vivo effective vascular permeability in murine lymph nodes.
  • Administered vascular endothelial growth factor-A (VEGF-A) to increase vascular permeability.
  • Quantified chemotherapeutic drug concentrations using HPLC in various tissues.

Main Results:

  • VEGF-A significantly increased lymph node blood vessel effective vascular permeability (approximately fourfold).
  • No significant difference in lymph node drug accumulation was observed between VEGF-A treated and untreated groups.
  • Chemotherapy penetration into lymph nodes was not enhanced by VEGF-A pretreatment.

Conclusions:

  • Lymph node vascular permeability is modifiable by VEGF-A.
  • Increasing vascular permeability alone does not guarantee improved chemotherapy uptake in lymph nodes.
  • Further strategies are needed to enhance drug delivery to lymph node metastases.