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Increase of tumour infiltrating lymphocytes in mice treated with antimetastatic doses of NAMI-A.

Abstract
NAMI-A is a novel antitumour agent, based on ruthenium, which has proved effectiveness against lung metastases of solid mouse tumours. The study focuses on the effects of NAMI-A on leukocyte infiltration into the primary tumour of MCa mammary carcinoma, implanted subcutaneously (s.c.) or intramuscularly (i.m.) into CBA mice. NAMI-A, given with a cycle of daily treatments for six consecutive days on advanced tumours at 35 mg/kg/day, markedly reduces lung metastasis independently of the tumour type (Lewis lung carcinoma, MCa mammary carcinoma or TS/A adenocarcinoma) being treated and of the site of tumour implantation (s.c. or i.m.). The analysis of leukocyte infiltration of the primary tumour, performed on a single cell suspension of cells isolated from a Ficoll gradient on which a raw suspension of primary tumour cells was layered, showed NAMI-A to significantly increase tumour infiltrating lymphocytes. These lymphocytes are almost all CD3+ cells with a significant increase of the CD8+ over the CD4+ subpopulation that reduces the helper/suppressor ratio from 2.8 to 2.1. These data indicated the absence of toxicity of NAMI-A for tumour infiltrating lymphocytes and suggested that this compound might even synergize in combined treatments with cancer immunotherapy.
AuthorsM Magnarin, A Bergamo, M E Carotenuto, S Zorzet, G Sava
JournalAnticancer research (Anticancer Res) 2000 Sep-Oct Vol. 20 Issue 5A Pg. 2939-44 ISSN: 0250-7005 [Print] Greece
PMID11062704 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Organometallic Compounds
  • Ruthenium Compounds
  • imidazolium-bis(imidazole)dimethylsulfoxideimidazotetrachlororuthenate(III)
  • Dimethyl Sulfoxide
Topics
  • Adenocarcinoma (drug therapy, immunology)
  • Animals
  • Antineoplastic Agents (therapeutic use)
  • Carcinoma, Lewis Lung (drug therapy, immunology)
  • Dimethyl Sulfoxide (analogs & derivatives, therapeutic use)
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Lung Neoplasms (immunology, prevention & control, secondary)
  • Lymphocytes, Tumor-Infiltrating (immunology)
  • Mammary Neoplasms, Experimental (drug therapy, immunology)
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred CBA
  • Organometallic Compounds (therapeutic use)
  • Ruthenium Compounds
  • T-Lymphocytes (classification, immunology)

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