Hanauske A-R, Sundell Karen, Lahn Michael
Department of Medicine, AK St. Georg, Lohmühlenstrasse 5, D-20099 Hamburg, FR-Germany.
Curr Pharm Des. 2004;10(16):1923-36. doi: 10.2174/1381612043384376.
As our understanding of tumorigenesis increases, interference with the various signaling pathways of tumor cells has become an attractive approach to arresting tumor cell growth and overcoming chemoresistance. Among many intracellular signaling proteins, protein kinase C (PKC) isoenzymes have been identified as possible targets to render tumor cells more susceptible to apoptosis and growth arrest. We review the known biology of the alpha-isoenzyme of PKC in different cancers to provide a rational approach for developing targeted therapies using PKC modulators, including aprinocarsen, an antisense oligonucleotide (ASO) against PKC-alpha.
随着我们对肿瘤发生机制的理解不断加深,干扰肿瘤细胞的各种信号通路已成为抑制肿瘤细胞生长和克服化疗耐药性的一种有吸引力的方法。在众多细胞内信号蛋白中,蛋白激酶C(PKC)同工酶已被确定为可能的靶点,以使肿瘤细胞更易发生凋亡和生长停滞。我们综述了PKCα同工酶在不同癌症中的已知生物学特性,为开发使用PKC调节剂(包括针对PKCα的反义寡核苷酸阿普瑞司)的靶向治疗提供合理的方法。