Kuroki Tamotsu, Tajima Yoshitsugu, Matsuo Kei, Kanematsu Takashi
Department of Transplantation and Digestive Surgery, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan.
Surg Today. 2005;35(2):101-5. doi: 10.1007/s00595-004-2906-2.
Gallbladder carcinoma is an aggressive cancer associated with a poor prognosis. Unfortunately, the precise molecular mechanisms of development and progression of this highly malignant tumor remain unknown. It is still unclear whether loss of heterozygosity (LOH) plays a significant role in gallbladder carcinogenesis, but recent studies have found a high incidence of LOH at several chromosomes in gallbladder carcinoma. In particular, LOH on chromosomes 1p, 3p, 5p, 8p, 9p, 9q, 13q, 16q, and 17p has been highlighted and LOH on 3p, 9p, 13q, 16q, and 17p has been detected in preneoplastic lesions and in the early phase of gallbladder carcinoma during multistep carcinogenesis. The proto-oncogene, K-ras, is the best known genetic alteration in several human neoplasms, including gallbladder carcinoma. The accumulation of these genetic changes leads to a disruption in cell-cycle regulation and also continuous cell proliferation. We present an overview of K-ras alteration and LOH at several chromosome loci in gallbladder carcinoma. Further studies of the molecular mechanism in gallbladder carcinoma and the delineation of the genetic influence involved should promote our understanding of gallbladder carcinogenesis.
胆囊癌是一种侵袭性癌症,预后较差。不幸的是,这种高度恶性肿瘤发生和进展的确切分子机制仍不清楚。杂合性缺失(LOH)在胆囊癌发生过程中是否起重要作用尚不清楚,但最近的研究发现胆囊癌中几个染色体上的LOH发生率很高。特别是,1p、3p、5p、8p、9p、9q、13q、16q和17p染色体上的LOH已受到关注,并且在多步骤致癌过程中的癌前病变和胆囊癌早期阶段已检测到3p、9p、13q、16q和17p染色体上的LOH。原癌基因K-ras是包括胆囊癌在内的几种人类肿瘤中最著名的基因改变。这些基因变化的积累导致细胞周期调控紊乱以及细胞持续增殖。我们概述了胆囊癌中K-ras改变和几个染色体位点上的LOH。对胆囊癌分子机制的进一步研究以及对所涉及的遗传影响的描述应有助于我们对胆囊癌发生的理解。