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关于 I 类 PI3K 催化亚基表达模式及其在结直肠癌中的预后意义的研究。

Studies on the expression patterns of class I PI3K catalytic subunits and its prognostic significance in colorectal cancer.

机构信息

Department of Colorectal Surgery, The Affiliated 3rd Hospital, Harbin Medical University, Harbin, People's Republic of China.

出版信息

Cell Biochem Biophys. 2012 Jan;62(1):47-54. doi: 10.1007/s12013-011-9257-6.

Abstract

The phosphatidylinositol 3-kinase/AKT (PI3K/AKT) pathway plays a critical role in human cancer. We determined the expression patterns of class I PI3K catalytic subunits and evaluated their importance in the development or progression of colorectal cancer (CRC). For this purpose, expression of class I PI3K isoforms was evaluated in 82 primary CRC and paired non-cancerous mucosa samples by qRT-PCR. P-AKT-Ser473 and P-AKT-Thr308 expression were measured by western blot. We found that, compared with paired non-cancerous mucosa samples, mRNA expression of p110α and p110β in CRCs was significantly increased to 2.02-fold (95% confidence interval [CI] 1.25-3.28 fold) and 1.76-fold (95% CI 1.19-2.60 fold), respectively; while slight differences were found regarding the expression of p110δ (0.57-fold; 95% CI 0.31-1.07 fold) and p110γ (0.97-fold; 95% CI 0.50-1.88 fold). Increased p110α and p110β expression correlated with primary tumor size, regional lymph node metastases, and AJCC stage. Increased p110β expression also correlated with distant metastasis. P-AKT-Thr308 and P-AKT-Ser473 expression showed significant direct correlations with p110α and p110β mRNA expression. Besides, CRC patients with p110β mRNA overexpression had a worse disease-free survival after radical surgery compared with those with normal or decreased levels (P = 0.043). It was, therefore, concluded that the altered p110α and p110β expression might contribute to the CRC development or progression.

摘要

磷脂酰肌醇 3-激酶/蛋白激酶 B(PI3K/AKT)通路在人类癌症中起着关键作用。我们确定了 I 类 PI3K 催化亚基的表达模式,并评估了它们在结直肠癌(CRC)发生或发展中的重要性。为此,我们通过 qRT-PCR 评估了 82 例原发性 CRC 和配对非癌性黏膜样本中 I 类 PI3K 同工型的表达。通过 Western blot 测量 P-AKT-Ser473 和 P-AKT-Thr308 的表达。我们发现,与配对非癌性黏膜样本相比,CRC 中 p110α 和 p110β 的 mRNA 表达分别显著增加了 2.02 倍(95%置信区间 [CI] 1.25-3.28 倍)和 1.76 倍(95% CI 1.19-2.60 倍);而 p110δ 的表达差异较小(0.57 倍;95% CI 0.31-1.07 倍)和 p110γ(0.97 倍;95% CI 0.50-1.88 倍)。p110α 和 p110β 表达增加与原发肿瘤大小、区域淋巴结转移和 AJCC 分期有关。p110β 表达增加也与远处转移有关。P-AKT-Thr308 和 P-AKT-Ser473 的表达与 p110α 和 p110β mRNA 表达呈显著正相关。此外,与正常或降低水平相比,p110β mRNA 过表达的 CRC 患者在根治性手术后无病生存率更差(P = 0.043)。因此,我们得出结论,改变的 p110α 和 p110β 表达可能有助于 CRC 的发生或发展。

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