Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis.

Increased interferon alpha receptor 2 mRNA levels is associated with renal cell carcinoma metastasis.
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DOI:
10.1186/1471-2407-7-159
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发表时间:
2007-08-15
期刊:
影响因子:
3.8
通讯作者:
Yoshida, Ken-Ichiro
Yoshida, Ken-Ichiro
中科院分区:
医学2区
文献类型:
--
作者:
Kamai, Takao;Yanai, Yoshiaki;Arai, Kyoko;Abe, Hideyuki;Yamanishi, Tomonori;Kurimoto, Masashi;Yoshida, Ken-Ichiro

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Interferon-α (IFN-α) is one of the central agents in immunotherapy for renal cell carcinoma (RCC) and binds to the IFN-α receptor (IFNAR). We investigated the role of IFNAR in RCC. We quantified IFNAR mRNA expression in paired tumor and non-tumor samples from the surgical specimens of 103 consecutive patients with RCC using a real-time reverse transcription polymerase chain reaction (RT-PCR), and IFNAR2 protein using Western blotting. The absolute level of IFNAR1 and IFNAR2 mRNAs in tumor and non-tumor tissues did not correlate with the malignant and metastatic profiles. The relative yields of the PCR product from the tumor tissue to that from the corresponding non-tumor tissue (T/N) for the expression of IFNAR mRNAs were calculated. While the T/N ratio of IFNAR1 did not correlate with any factor, a high T/N ratio of IFNAR2 correlated with poor differentiation (P < 0.05), local invasion (P < 0.001), and metastasis (P < 0.0001). By multivariate analysis, a high T/N ratio of IFNAR2 predicted a shortened overall survival in all cases (P < 0.05) and a shorter disease-free survival in those without metastasis (M0; 68 cases, P < 0.05). Impressively, patients with a poorer response to IFN-α treatment had a higher IFNAR2 T/N ratio than those who had a good response (P < 0.05). IFNAR2c protein expression was higher in the primary tumors in patients with metastases (M1; 35 cases) compared to those without ( P < 0.0001). IFNAR2 is associated with the progression of RCC.
通过与皮下干扰素 - 阿尔法和动脉内5-氟尿嘧啶联合治疗,用主要门静脉血栓形成治疗肝细胞癌癌; 1型干扰素受体表达的作用。
DOI: 10.1038/sj.bjc.6602742
发表时间: 2005-09-05
影响因子: 8.8
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通讯作者: --
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发表时间: 1999-08-01
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