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Lung cancer epigenetics and genetics.肺癌的表观遗传学与遗传学
Int J Cancer. 2008 Jul 1;123(1):1-7. doi: 10.1002/ijc.23605.
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Osteoporotic bone formation in mice lacking tob2; involvement of Tob2 in RANK ligand expression and osteoclasts differentiation.缺乏Tob2的小鼠中的骨质疏松性骨形成;Tob2在RANK配体表达和破骨细胞分化中的作用。
FEBS Lett. 2008 Apr 16;582(9):1313-8. doi: 10.1016/j.febslet.2008.03.012. Epub 2008 Mar 20.
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The BTG2 protein is a general activator of mRNA deadenylation.BTG2蛋白是一种mRNA去腺苷酸化的通用激活剂。
EMBO J. 2008 Apr 9;27(7):1039-48. doi: 10.1038/emboj.2008.43. Epub 2008 Mar 13.
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The candidate tumor suppressor BTG3 is a transcriptional target of p53 that inhibits E2F1.候选抑癌基因BTG3是p53的转录靶点,可抑制E2F1。
EMBO J. 2007 Sep 5;26(17):3968-80. doi: 10.1038/sj.emboj.7601825. Epub 2007 Aug 9.
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Homozygous deletion scanning of the lung cancer genome at a 100-kb resolution.以100千碱基对分辨率对肺癌基因组进行纯合缺失扫描。
Genes Chromosomes Cancer. 2007 Nov;46(11):1000-10. doi: 10.1002/gcc.20485.
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Prevalence and specificity of LKB1 genetic alterations in lung cancers.肺癌中LKB1基因改变的患病率和特异性
Oncogene. 2007 Aug 30;26(40):5911-8. doi: 10.1038/sj.onc.1210418. Epub 2007 Mar 26.
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Loss of B-cell translocation gene-2 in estrogen receptor-positive breast carcinoma is associated with tumor grade and overexpression of cyclin d1 protein.雌激素受体阳性乳腺癌中B细胞易位基因-2的缺失与肿瘤分级及细胞周期蛋白D1蛋白的过表达相关。
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The complex between urokinase (uPA) and its type-1 inhibitor (PAI-1) in pulmonary adenocarcinoma: relation to prognosis.肺腺癌中尿激酶(uPA)与其1型抑制剂(PAI-1)之间的复合物:与预后的关系。
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E1B-deleted adenovirus replicates in p53-deficient lung cancer cells due to the absence of apoptosis.E1B 缺失的腺病毒由于缺乏细胞凋亡而在 p53 缺陷的肺癌细胞中复制。
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Tissue MMP-2 and MMP-9 [corrected] are better prognostic factors than serum MMP-2/TIMP-2--complex or TIMP-1 [corrected] in stage [corrected] I-III lung carcinoma.在I - III期肺癌中,组织基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶-9比血清MMP-2/TIMP-2复合物或基质金属蛋白酶抑制剂-1(TIMP-1)是更好的预后因素。
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增殖抑制家族蛋白 Ana 的缺乏与肺腺癌的发生有关。

Deficiency of antiproliferative family protein Ana correlates with development of lung adenocarcinoma.

机构信息

Division of Oncology, Department of Cancer Biology, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo, Japan.

出版信息

Cancer Sci. 2009 Feb;100(2):225-32. doi: 10.1111/j.1349-7006.2008.01030.x.

DOI:10.1111/j.1349-7006.2008.01030.x
PMID:19068083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11159387/
Abstract

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.

摘要

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。