Division of Oncology, Department of Cancer Biology, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo, Japan.
Cancer Sci. 2009 Feb;100(2):225-32. doi: 10.1111/j.1349-7006.2008.01030.x.
The abundant in neuroepithelium area (ana) gene was originally identified as a member of the tob/btg family of antiproliferative genes. Like the other family members, Ana inhibits growth of NIH3T3 cells when overexpressed. However, whether or not Ana is involved in tumor progression has been elusive. Here, we show that expression of ana is relatively high in the lung, the expression being restricted in type II alveolar epithelial cells. We further show that ana expression is reduced in 97% of the human lung cancer cell lines examined (61/63) and 86% of clinical samples from lung adenocarcinoma patients (36/42). Long-term observation of ana-deficient (ana−/–) mice reveals that 8% of them develop lung tumors (5/66) by 21 months after birth, while 0% of wild-type mice (0/35) develop the same type of tumors. We also show that exogenously expressed ana gene product suppresses the levels of matrix metalloproteinase-2 (MMP-2) and plasminogen activator inhibitor-1 (PAI-1) expression in lung cancer cells. Taken together, we propose that ana functions as a tumor suppressor and that its product inhibits tumor progression as well by suppressing angiogenesis, invasion, and metastasis.
神经上皮区域(ana)基因最初被鉴定为 Tob/btg 家族抗增殖基因的成员。与其他家族成员一样,Ana 过表达时会抑制 NIH3T3 细胞的生长。然而,Ana 是否参与肿瘤进展一直难以捉摸。在这里,我们表明 ana 在肺部的表达相对较高,表达仅限于 II 型肺泡上皮细胞。我们进一步表明,ana 的表达在 97%的人肺癌细胞系(61/63)和 86%的肺腺癌患者临床样本(36/42)中降低。对 ana 缺陷(ana−/–)小鼠的长期观察表明,出生后 21 个月,有 8%的小鼠(5/66)发展为肺癌,而野生型小鼠(0/35)则没有发展为相同类型的肿瘤。我们还表明,外源性表达的 ana 基因产物可抑制肺癌细胞中基质金属蛋白酶-2(MMP-2)和纤溶酶原激活物抑制剂-1(PAI-1)的表达水平。综上所述,我们提出 ana 作为肿瘤抑制因子的作用,其产物通过抑制血管生成、侵袭和转移来抑制肿瘤进展。