Boente M P, Hurteau J, Rodriguez G C, Bast R C, Berchuck A
Duke University Medical Center, Durham, North Carolina.
Curr Opin Oncol. 1993 Sep;5(5):900-7. doi: 10.1097/00001622-199309000-00020.
Recent studies have begun to elucidate the molecular events involved in the development of ovarian cancer. First, it has been shown that epithelial ovarian cells both produce and have receptors for many peptide growth factors. It is possible that these growth factors may participate in autocrine and paracrine growth-regulatory pathways in these cells. Increased activity of stimulatory factors, eg, transforming growth factor-alpha, or decreased activity of inhibitor factors, eg, transforming growth factor-beta, may facilitate malignant transformation. In addition, it has been shown that ovarian cancer cells often have acquired the ability to degrade extracellular matrix and invade the underlying tissues. Finally, alterations in several oncogenes and tumor-suppressor genes, including HER2/neu, c-myc, and p53, have been found in ovarian cancers. Although exciting insights into the molecular pathology of ovarian cancer have been gained, we remain far from a comprehensive understanding of the biology of this highly lethal disease.
最近的研究已开始阐明卵巢癌发生发展过程中涉及的分子事件。首先,已表明上皮性卵巢细胞既能产生多种肽生长因子,又有这些因子的受体。这些生长因子有可能参与这些细胞的自分泌和旁分泌生长调节途径。刺激因子(如转化生长因子-α)活性增加,或抑制因子(如转化生长因子-β)活性降低,可能会促进恶性转化。此外,已表明卵巢癌细胞常常获得了降解细胞外基质并侵入下方组织的能力。最后,在卵巢癌中发现了几种癌基因和肿瘤抑制基因的改变,包括HER2/neu、c-myc和p53。尽管已在卵巢癌分子病理学方面获得了令人兴奋的见解,但我们对这种高致死性疾病的生物学特性仍远未全面了解。