Kim Suwon, Chin Koei, Gray Joe W, Bishop J Michael
The G. W. Hooper Research Foundation and Department of Microbiology and Immunology, Department of Laboratory Medicine and Comprehensive Cancer Center, University of California, San Francisco, CA 94143, USA.
Proc Natl Acad Sci U S A. 2004 Nov 16;101(46):16251-6. doi: 10.1073/pnas.0407158101. Epub 2004 Nov 4.
We have devised a screen for genes that suppress the loss of contact inhibition elicited by overexpression of the protooncogene MYCN. The initial application of this screen detected nine distinctive suppressors within a representative human cDNA library. One of these genes was ING4, a potential tumor suppressor gene that maps to human chromosome 12p13. Ectopic expression of ING4 suppressed the loss of contact inhibition elicited by either MYCN or MYC but had no direct effect on cellular proliferation. Pursuing the possibility that ING4 might be a tumor suppressor gene, we found inactivating mutations in ING4 transcripts from various human cancer cell lines. In addition, we used comparative genomic hybridization to detect deletion of the ING4 locus in 10-20% of human breast cancer cell lines and primary breast tumors. Ectopic expression of ING4 attenuated the growth of T47D human breast cancer cells in soft agar. We conclude that ING4 is a strong candidate as a tumor suppressor gene.
我们设计了一种筛选方法,用于筛选能够抑制由原癌基因MYCN过表达所引发的接触抑制丧失的基因。该筛选方法的初步应用在一个具有代表性的人类cDNA文库中检测到了9种不同的抑制因子。其中一个基因是ING4,它是一个潜在的肿瘤抑制基因,定位于人类染色体12p13。ING4的异位表达抑制了由MYCN或MYC引发的接触抑制丧失,但对细胞增殖没有直接影响。考虑到ING4可能是一个肿瘤抑制基因,我们在多种人类癌细胞系的ING4转录本中发现了失活突变。此外,我们使用比较基因组杂交技术在10%-20%的人类乳腺癌细胞系和原发性乳腺肿瘤中检测到ING4基因座的缺失。ING4的异位表达减弱了T47D人乳腺癌细胞在软琼脂中的生长。我们得出结论,ING4是作为肿瘤抑制基因的有力候选者。