Department of Colorectal Surgery, The Affiliated 3rd Hospital, Harbin Medical University, Harbin, People's Republic of China.
Cell Biochem Biophys. 2012 Jan;62(1):47-54. doi: 10.1007/s12013-011-9257-6.
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.
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。