Perugini R A, McDade T P, Vittimberga F J, Callery M P
Department of Surgery, University of Massachusetts-Memorial Health System, Worcester, USA.
Crit Rev Eukaryot Gene Expr. 1998;8(3-4):377-93. doi: 10.1615/critreveukargeneexpr.v8.i3-4.70.
Adenocarcinoma of the pancreas carries a grave prognosis for affected patients. Certain oncogenes (K-ras and HER-2/neu) are mutated in a large proportion of these aggressive tumors. Adenocarcinoma of the pancreas has also been associated with loss of tumor suppressor genes (p53, DPC4, p16/MTS), either by deletion or by mutation and loss of function. Growth factors (EGF, TGF-alpha, HGF) and growth factor receptors (EGF-R, c-met, CCK) are expressed at levels not found in the normal pancreas. Finally, factors important for angiogenesis (FGF, integrins, selectins) are likely to play an important role in the growth and metastasis of clinically relevant tumors. This review attempts to summarize and assimilate current research into the molecular and cellular biology of pancreatic cancer.
胰腺腺癌给患者带来严峻的预后。在这些侵袭性肿瘤中,某些癌基因(K-ras和HER-2/neu)有很大比例发生突变。胰腺腺癌还与肿瘤抑制基因(p53、DPC4、p16/MTS)的缺失有关,其缺失方式包括基因缺失、突变及功能丧失。生长因子(EGF、TGF-α、HGF)和生长因子受体(EGF-R、c-met、CCK)的表达水平在正常胰腺中未被发现。最后,对血管生成很重要的因子(FGF、整合素、选择素)可能在临床相关肿瘤的生长和转移中发挥重要作用。本综述试图总结和整合目前关于胰腺癌分子和细胞生物学的研究。