52. Expression of cancer stem cell markers in primary lesion and lymphatic metastatic lesions of gastric carcinoma
Objective: To study on expressions and clinical significances
of cancer stem cell marker CD133, EpCAM, ABCG2, Oct4
in primary lesion and lymphatic metastatic lesions of gastric
carcinoma.
Methods: From 2009 to 2011, 36 paraffin samples of gastric
carcinoma were obtained. Expressions of four markers were
detected in primary lesions (36 cases), in noncancerous
gastric mucosa tissue (30 cases) and in lymphatic metastatic
lesions (25 cases) by immunohistochemical staining (IHC).
Correlations of proteins expressions with clinicopathological
parameters were analyzed.
Results: Expressions of CD133, EpCAM, ABCG2 and Oct4
in gastric carcinoma tissues were significantly higher than
that of adjacent tissue (P<0.05). Expressions of CD133 was
significantly higher in subgroups with severer invasion depth
(P=0.029), severer lymph node metastasis (P=0.020) and later
TNM stage (P=0.001). Expressions of EpCAM was significantly
higher in subgroups with severer invasion depth (P=0.022).
Expressions of ABCG2 was significantly higher in subgroups
with lower differentiation of tumor (P=0.042), severer invasion
depth (P=0.020) and later TNM stage (P=0.035). Expressive
rates of CD133, EpCAM and ABCG2 in lymphatic metastatic
lesions were 28%, 60% and 44%, lower than that in primary
lesion (P<0.05). Expression of EpCAM in lymphatic metastatic
lesions was significantly higher in subgroups with higher primary
lesion expression (P=0.040).
Conclusions: Expressions of CD133, EpCAM, ABCG2 and
Oct4 in gastric carcinoma tissues were significantly higher than
that of adjacent tissue. These markers may be regarded as markers
of gastric carcinoma. Higher expressive level of CD133 and
EpCAM is related with severer advanced gastric cancer. Higher
expressive level of ABCG2 is related with lower differentiation of
tumor and severer advanced gastric cancer. These four markers
express in lymphatic metastatic lesions of gastric carcinoma.
Higher expressive level of EpCAM in lymphatic metastatic
lesions is associated to higher primary lesion expression.
Key words
Cancer stem cell; primary lesion; lymphatic metastatic lesions; gastric carcinoma