Bregman M D, Sipes N J
Int J Cell Cloning. 1986 Jul;4(4):224-36. doi: 10.1002/stem.5530040401.
Cellular transformation may be accomplished in vitro and in vivo through the concerted action of growth factors and oncogenes. This association has demonstrated that malignant growth results from aberrations in growth factor-signal transduction pathways that normally operate to control proliferation. Activation of genes that code for growth factors and/or their receptors provides tumor cells with potential mechanisms to maintain their proliferative state. Tumor cells have been shown to produce endogenous substances that augment their growth (autocrine stimulation), as well as responding to exogenous substances (paracrine stimulation). With solid tumor cells these responses have been shown to involve aberrant expression of growth factor and/or receptor genes. The study of the interrelationship of these various growth regulatory molecules is important not only in the identification of gene products essential to cellular proliferation, but also in providing clues as to what forces are driving tumor cell growth.
细胞转化可通过生长因子和癌基因的协同作用在体外和体内实现。这种关联表明,恶性生长源于正常情况下控制增殖的生长因子信号转导途径的异常。编码生长因子和/或其受体的基因的激活为肿瘤细胞提供了维持其增殖状态的潜在机制。已证明肿瘤细胞会产生促进其生长的内源性物质(自分泌刺激),以及对外源性物质作出反应(旁分泌刺激)。对于实体瘤细胞,这些反应已被证明涉及生长因子和/或受体基因的异常表达。研究这些各种生长调节分子之间的相互关系不仅对于鉴定细胞增殖所必需的基因产物很重要,而且对于揭示驱动肿瘤细胞生长的因素也很重要。