Dhar Animesh, Mehta Smita, Banerjee Snigdha, Dhar Kakali, Dhar Gopal, Sengupta Krishanu, Ray Gibanananda, Banerjee Sushanta K, Campbell Donald R
Cancer Research Unit, Department of Veterans Affairs Medical Center, 4801 East Linwood Boulevard, Kansas City, MO 64128-2226, USA.
Front Biosci. 2005 May 1;10:1763-7. doi: 10.2741/1659.
Expression of epidermal growth factor receptors (EGFR) is exaggerated in pancreatic adenocarcinoma and activation of EGFR appears to have an important role in the growth and differentiation of this and in other tumors. Therefore, blockade or inactivation of EGFR by monoclonal antibodies or by tyrosine kinase inhibitors has significant potential as an effective anti-cancer therapy. One of the very recent significant developments in the field of molecular biology involves the use of antisense of EGFR or EGFR gene silencing in pancreatic cancer cells as a potential targeted therapy for patients with pancreatic adenocarcinoma.
表皮生长因子受体(EGFR)在胰腺腺癌中过度表达,EGFR的激活似乎在该肿瘤以及其他肿瘤的生长和分化中发挥重要作用。因此,通过单克隆抗体或酪氨酸激酶抑制剂阻断或失活EGFR作为一种有效的抗癌疗法具有巨大潜力。分子生物学领域最近的一项重大进展涉及在胰腺癌细胞中使用EGFR反义核酸或EGFR基因沉默作为胰腺腺癌患者的潜在靶向治疗方法。