| Literature DB >> 19967055 |
Nikolai Nikolaevich Belyaev1, Andrei-Yurievich Bogdanov, Philipp-Georgievich Savvulidi, Vladimir-Konstantinovich Krasnoshtanov, Raikhan-Tleulievna Tleulieva, Gabit-Kaimovich Alipov, Ichiro Sekine, Jun-Sang Bae, Jeong-Beom Lee, Young-Ki Min, Hun-Mo Yang.
Abstract
The influence of alpha-fetoprotein (AFP) on the bone marrow (BM) natural suppressor (NS) cells of intact Ehrlich carcinoma -bearing CBA mice was studied. Bone marrow NS cells were fractionated into three fractions by isopycnic centrifugation on percoll gradients: NS1 (rho=1.080 g/ml), NS2 (rho=1.090 g/ml) and NS3 (1.100>rho>1.090 g/ml). These fractions were highly different in their sensitivity to known NS cell inductors (interleukin (IL)-2, IL-3 or histamine). None of the NS fractions isolated from the intact mice spontaneously produced antiproliferative activity, however, they showed a high level of NS (antiproliferative and natural killer cell inhibitory) activity under the influence of AFP. A single injection of AFP to intact mice led to an increase of spontaneous NS activity and the inhibition of natural killer cell activity. NS activity, especially NS2, was increased in when tumor cells were subcutaneously inoculated three days after AFP injection. In the AFP-treated mice, the tumor mass at 14 days was 60% larger than that in the untreated mice. Our data confirmed that AFP is a tumor marker that can inhibit cancer immunity and plays a role in cancer pathogenesis.Entities:
Keywords: Alpha-fetoprotein (AFP); Ehrlich carcinoma (EC); Natural killer cells; Natural suppressor (NS) cells
Year: 2008 PMID: 19967055 PMCID: PMC2788635 DOI: 10.4196/kjpp.2008.12.4.193
Source DB: PubMed Journal: Korean J Physiol Pharmacol ISSN: 1226-4512 Impact factor: 2.016