Regulation and clinical significance of the hypoxia-induced expression of ANGPTL4 in gastric cancer

被引:31
作者
Kubo, Hiroshi [1 ]
Kitajima, Yoshihiko [1 ,2 ]
Kai, Keita [3 ]
Nakamura, Jun [1 ]
Miyake, Shuusuke [1 ]
Yanagihara, Kazuyoshi [4 ]
Morito, Kiyoto [1 ]
Tanaka, Tomokazu [1 ]
Shida, Masaaki [1 ]
Noshiro, Hirokazu [1 ]
机构
[1] Saga Univ, Fac Med, Dept Surg, 5-1-1 Nabeshima, Saga 8498501, Japan
[2] Natl Hosp Org, Dept Surg, Higashisaga Hosp, Saga 8490101, Japan
[3] Saga Univ, Fac Med, Dept Pathol & Biodef, Saga 8498501, Japan
[4] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, Div Translat Res, Kashiwa, Chiba 2778577, Japan
关键词
ANGPTL4; HIF-1; gastric cancer; hypoxia; ANGIOPOIETIN-LIKE; 4; PROMOTES VENOUS INVASION; COLORECTAL-CANCER; VASCULAR-PERMEABILITY; LIPOPROTEIN-LIPASE; KAPOSIS-SARCOMA; PROTEIN; METASTASIS; ANGIOGENESIS; HIF-1-ALPHA;
D O I
10.3892/ol.2015.4011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Solid tumors are often exposed to hypoxia. Hypoxia inducible factor (HIF)-1 alpha upregulates numerous target genes associated with the malignant behavior of hypoxic cancer cells. A member of the angiopoietin family, angiopoietin-like protein 4 (ANGPTL4) is a hypoxia-inducible gene. The present study aimed to clarify whether ANGPTL4 is regulated by HIF-1a in gastric cancer cells. The study also assessed whether ANGPTL4 expression is associated with clinicopathological factors or HIF-1 alpha expression in gastric cancer tissues. Hypoxia-induced ANGPTL4 expression was quantitatively analyzed using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) in 10 gastric cancer cell lines. RT-qPCR was further employed to investigate the HIF-1 alpha dependency of ANGPTL4 expression using HIF-1 alpha-knockdown transfectant 58As9-KD and control 58As9-SC gastric cancer cells. The HIF-1 alpha and ANGPTL4 expression levels were immunohistochemically analyzed in 170 gastric cancer tissue specimens and were assessed for any correlations with the clinicopathological factors and/or patient survival. Subsequently, hypoxia-induced ANGPTL4 expression was observed in 7 out of 10 gastric cancer cell lines. The hypoxic induction of ANGPTL4 was almost preserved in the 58As9-KD cells compared with that observed in the 58As9-SC cells, while the induction of known HIF-1 alpha target gene, carbonic anhydrase 9, was completely suppressed in the 58As9-KD cells. In the gastric cancer tissues, ANGPTL4 expression was inversely correlated with the tumor depth, whereas HIF-1 alpha expression was positively correlated with venous invasion. A survival analysis revealed that the expression of ANGPTL4 was significantly correlated with a longer survival time, whereas that of HIF-1 alpha was correlated with a shorter survival time. In conclusion, the present findings indicate that hypoxia-induced ANGPTL4 expression is independent of HIF-1 alpha in hypoxic gastric cancer cells. ANGPTL4 may be a favorable marker for predicting a long survival time, whereas HIF-1 alpha predicts a poor prognosis, in gastric cancer patients. The hypoxic environment independently induces ANGPTL4 and HIF-1 alpha, which are believed to exhibit adverse effects on tumor progression.
引用
收藏
页码:1026 / 1034
页数:9
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