Chen Chun-Ming, Behringer Richard R
Department of Molecular Genetics, University of Texas, MD Anderson Cancer Center, Houston, Texas 77030, USA.
Genes Dev. 2004 Feb 1;18(3):320-32. doi: 10.1101/gad.1162204. Epub 2004 Jan 26.
Loss of OVCA1/DPH2L1 correlates with ovarian and breast cancer. To study its in vivo role, we generated Ovca1 mutant alleles in mice. Ovca1 heterozygotes spontaneously develop cancer. Ovca1 mutant mice die during embryonic development and at birth with developmental delay and defects in multiple organ systems. Cell proliferation defects were observed in Ovca1 mutant mouse embryonic fibroblasts (MEFs). p53 deficiency can rescue these Ovca1 mutant MEF proliferation defects and partially rescue Ovca1 mutant embryonic phenotypes. Furthermore, Ovca1; p53 double heterozygotes developed tumors quicker than p53 heterozygotes and with an increased carcinoma incidence. Multiple tumor burden in Ovca1 heterozygotes that were also p53 deficient was significantly higher than in p53 homozygous mutants. These in vivo findings demonstrate that Ovca1 is a tumor suppressor that can modify p53-induced tumorigenesis and suggest that it acts as a positive regulator for cell cycle progression. The close linkage of OVCA1 and p53 on human Chromosome 17 suggests that coordinated loss may be an important mechanism for the evolution of ovarian, breast, and other tumor phenotypes.
OVCA1/DPH2L1的缺失与卵巢癌和乳腺癌相关。为了研究其在体内的作用,我们在小鼠中生成了Ovca1突变等位基因。Ovca1杂合子会自发患癌。Ovca1突变小鼠在胚胎发育期间及出生时死亡,伴有发育延迟和多器官系统缺陷。在Ovca1突变小鼠胚胎成纤维细胞(MEF)中观察到细胞增殖缺陷。p53缺陷可挽救这些Ovca1突变MEF的增殖缺陷,并部分挽救Ovca1突变胚胎表型。此外,Ovca1;p53双杂合子比p53杂合子更快地发生肿瘤,且癌发病率增加。同时也是p53缺陷的Ovca1杂合子中的多种肿瘤负荷显著高于p53纯合突变体。这些体内研究结果表明,Ovca1是一种肿瘤抑制因子,可改变p53诱导的肿瘤发生,并表明它作为细胞周期进程的正调控因子发挥作用。人17号染色体上OVCA1和p53的紧密连锁表明,协同缺失可能是卵巢癌、乳腺癌及其他肿瘤表型演变的重要机制。