Related Experiment Video
Updated: Apr 21, 2026

Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo
Published on: July 20, 2019
Neem leaf glycoprotein prophylaxis transduces immune dependent stop signal for tumor angiogenic switch within tumor
Saptak Banerjee1, Tithi Ghosh1, Subhasis Barik1
1Department of Immunoregulation and Immunodiagnostics, Chittaranjan National Cancer Institute (CNCI), Kolkata, India.
Abstract:
We have reported that prophylactic as well as therapeutic administration of neem leaf glycoprotein (NLGP) induces significant restriction of solid tumor growth in mice. Here, we investigate whether the effect of such pretreatment (25µg/mice; weekly, 4 times) benefits regulation of tumor angiogenesis, an obligate factor for tumor progression. We show that NLGP pretreatment results in vascular normalization in melanoma and carcinoma bearing mice along with downregulation of CD31, VEGF and VEGFR2. NLGP pretreatment facilitates profound infiltration of CD8+ T cells within tumor parenchyma, which subsequently regulates VEGF-VEGFR2 signaling in CD31+ vascular endothelial cells to prevent aberrant neovascularization. Pericyte stabilization, VEGF dependent inhibition of VEC proliferation and subsequent vascular normalization are also experienced. Studies in immune compromised mice confirmed that these vascular and intratumoral changes in angiogenic profile are dependent upon active adoptive immunity particularly those mediated by CD8+ T cells. Accumulated evidences suggest that NLGP regulated immunomodulation is active in tumor growth restriction and normalization of tumor angiogenesis as well, thereby, signifying its clinical translation.
Insights
Neem leaf glycoprotein (NLGP) pretreatment normalizes tumor blood vessels and restricts tumor growth. This effect is mediated by CD8+ T cells, highlighting NLGP
Area of Science:
- Immunology
- Oncology
- Biochemistry
Background:
- Neem leaf glycoprotein (NLGP) has demonstrated tumor growth restriction capabilities.
- Tumor angiogenesis is crucial for tumor progression and metastasis.
Purpose of the Study:
- To investigate NLGP's effect on tumor angiogenesis.
- To determine the immunomodulatory mechanisms underlying NLGP's anti-tumor effects.
Main Methods:
- Mice bearing melanoma and carcinoma were pretreated with NLGP.
- Analysis of tumor vascularization markers (CD31, VEGF, VEGFR2) and immune cell infiltration (CD8+ T cells).
- Studies in immune-compromised mice to confirm immune dependency.
Main Results:
- NLGP pretreatment normalized tumor vasculature and downregulated CD31, VEGF, and VEGFR2.
- Enhanced infiltration of CD8+ T cells into tumors was observed.
- NLGP-induced vascular normalization and tumor growth restriction were dependent on CD8+ T cell-mediated immunity.
Conclusions:
- NLGP effectively regulates tumor angiogenesis through immunomodulation, primarily via CD8+ T cells.
- NLGP demonstrates potential for clinical translation in cancer therapy by targeting tumor vascularization and immunity.
More Related Videos
12:42Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
10:49A Murine Cell Line Based Model of Chronic CDK9 Inhibition to Study Widespread Non-Genetic Transcriptional Elongation Defects TEdeff in Cancers
Published on: September 26, 2019
Related Concept Videos
Tumor Immunotherapy
Regulation of Angiogenesis and Blood Supply
The Tumor Microenvironment