Little expression of cytokine mRNA by fresh tumour-infiltrating mononuclear leukocytes from glioma and lung adenocarcinoma.

TitleLittle expression of cytokine mRNA by fresh tumour-infiltrating mononuclear leukocytes from glioma and lung adenocarcinoma.
Publication TypeJournal Article
Year of Publication1995
AuthorsGingras, M-C, Roussel, E, Roth, JA, Moser, RP
JournalCytokine
Volume7
Issue6
Pagination580-8
Date Published1995 Aug
ISSN1043-4666
KeywordsBase Sequence, Brain Neoplasms, Carcinoma, Non-Small-Cell Lung, Case-Control Studies, Cytokines, Gene Expression Regulation, Neoplastic, Glioblastoma, Humans, Image Processing, Computer-Assisted, Lung Neoplasms, Lymphocytes, Tumor-Infiltrating, Molecular Sequence Data, Polymerase Chain Reaction, Reference Values, Reproducibility of Results, RNA, Messenger
Abstract

We investigated whether cytokine genes were activated in human tumour-infiltrating mononuclear leukocytes (TIML) obtained from six lung adenocarcinomas and seven glioblastomas. TIML were extracted by mechanical disruption and isolated by double density gradient of Ficoll. We performed mRNA reverse transcription-polymerase chain reaction (RT-PCR) on these fresh (noncultured) TIML and autologous peripheral blood mononuclear leukocytes (PBML) using primers for the cytokines IL-1 beta, IL-6, IL-2, IL-4, GM-CSF, IFN-gamma and TNF-beta. In addition, we compared patients' TIML and PBML populations with healthy normal and alpha-CD3 activated PBML as an optimally activated reference population. Gel bands of RT-PCR products were quantitated in relative units (RU) as a function of their size and intensity by computerized image-analysis. Lung and brain patients' TIML showed IL-1 beta and IL-6 cytokine mRNA expressed in the average of 2-log RU but not significantly different from autologous and normal healthy PBML. IL-2, IFN-gamma and TNF-beta also did not appear expressed in the TIML at higher levels than in autologous or healthy normal PBML. However in two thirds of patients, lung TIML could be distinguished from autologous PBML by specific expression of GM-CSF and from healthy normal PBML by expression of IL-4. Similarly, most brain TIML expressed mRNA significantly above healthy normal PBML for GM-CSF and IL-4. In comparison with alpha-CD3 activated healthy PBML, our results suggest that lung and brain TIML had detectable cytokine mRNA, but they seemed poorly activated in total number of genes and amount of cytokine mRNA.(ABSTRACT TRUNCATED AT 250 WORDS)

DOI10.1006/cyto.1995.0079
Alternate JournalCytokine
PubMed ID8580376
Grant List1P50-CA58204-03PP5 / CA / NCI NIH HHS / United States