Clinical impact of intratumoral natural killer cell and dendritic cell infiltration in gastric cancer
Citation
S. Ishigami et al., Clinical impact of intratumoral natural killer cell and dendritic cell infiltration in gastric cancer, CANCER LETT, 159(1), 2000, pp. 103-108
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CANCER LETTERS
SICI code
0304-3835(20001016)159:1<103:CIOINK>2.0.ZU;2-#
Abstract
Intratumoral natural killer cells (NKC) and dendritic cells IDC) may affect
the clinical features of various gastrointestinal cancers. However, the re
lationship between intratumoral NKC and DC remains unclear. We examined 169
patients with gastric cancer who underwent gastrectomy at Kagoshima Univer
sity Hospital. Immunohistochemical staining of CD57 and 5-100-protein was p
erformed to evaluate NKC and DC infiltration, respectively. A total of 25 a
reas containing pericancerous tissue were selected for determining the numb
er of NKC and DC under high power microscopy (x 400). Patients were classif
ied into two groups according to NKC and DC population. Intratumoral lympho
cytic infiltration was also calculated in 15 areas with a high power ( x 40
0) objective. The degree of NKC and DC infiltration was gradually decreased
according to the progression of nodal involvement. Patients with many NKC
infiltration had a lower positivity of lymph node metastasis and lymphatic
invasion than patients with little NKC infiltration. DC infiltration was al
so negatively correlated with depth of invasion. lymph node metastasis and
curativity. DC infiltration was positively correlated with lymphocytic infi
ltration (P = 0.01. r = 0.6). The 5-year survival rates of patients with ma
ny NKC infiltration and patients with DC many infiltration were 75 and 78%.
respectively, both of which were significantly better than that of patient
s with little NKC and DC infiltration (P < 0.05). NKC may be activated with
out DC or intratumoral lymphocytes. Intratumoral NKC may act as an independ
ent immunologic effector against tumor cells, unlike DC. (C) 2000 Elsevier
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