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CCL21 is an effective surgical neoadjuvant for treatment of mammary tumors
- Source :
- Cancer biologytherapy. 6(8)
- Publication Year :
- 2007
-
Abstract
- In previous studies, the chemokine CCL21 has shown biological activities that include T cell, natural killer (NK) cell, and dendritic cell (DC) chemoattraction. The goal of this study was to determine the effects of administering CCL21 to orthotopic mammary tumors in terms of impact on tumor growth rate, immune cell infiltration of the primary tumor and survival. We found that a single intratumoral administration of CCL21 slowed the growth of orthotopic mammary tumors and increased intratumoral infiltration by T cells, NK cells and DCs. CCL21 intratumoral administration also prolonged the survival of tumor-earing mice. Furthermore, mice that received intratumoral neoadjuvant CCL21 ior to surgical resection of tumors survived significantly longer than control mice. The urviving neoadjuvant CCL21-reated mice, when challenged again with cl-6, had significantly slower rate of tumor growth than challenged control mice. Thus, our ata indicate that CCL21 treatment prior to mammary tumor resection can significantly rolong survival and increase resistance to subsequent tumor challenge. Overall, our indings suggest that intratumoral administration of CCL21 has potential as a neoadjuvant mmunotherapy for breast cancer.
- Subjects :
- endocrine system
Cancer Research
Chemokine
Pathology
medicine.medical_specialty
T cell
T-Lymphocytes
Cell
Mammary Neoplasms, Animal
Mice
Lymphocytes, Tumor-Infiltrating
medicine
Animals
Pharmacology
Mammary tumor
Mice, Inbred BALB C
biology
Chemokine CCL21
business.industry
Dendritic cell
Dendritic Cells
medicine.disease
Primary tumor
Neoadjuvant Therapy
Killer Cells, Natural
medicine.anatomical_structure
Oncology
biology.protein
Molecular Medicine
Female
business
Infiltration (medical)
CCL21
Subjects
Details
- ISSN :
- 15558576
- Volume :
- 6
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- Cancer biologytherapy
- Accession number :
- edsair.doi.dedup.....b17dd47c40a6ded668c990854a4607cc