Zhao Shan-Chao, Zhou Bo-Wei, Luo Fei, Mao Xueying, Lu Yong-Jie
Department of Urology, Nanfang Hospital, Southern Medical University Guangzhou, PR China.
Molecular Oncology, Barts Cancer Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London London, UK.
Int J Clin Exp Med. 2015 Oct 15;8(10):17072-9. eCollection 2015.
The deletion of chromosomal region 6q was commonly found in several types of human cancers, although the tumor suppressor genes (TSGs) located within this genomic region are not well established. Our recent work detected recurrent chromosomal truncation at the Na(+)/K(+) transporting ATPase interacting 2 (NKAIN2) gene in prostate cancer, which was also found to be truncated in leukemia and lymphoma, suggesting that NKAIN2 is potentially one of the TSGs located in the 6q commonly deleted region in human cancers. NKAIN2 gene consists of eight coding exons that span approximately 1 Mb of genomic DNA on chromosome 6q and there are four main splice variants. The function of this gene is not well investigated and the limited knowledge of this gene pointed to nervous system development. The chromosomal translocations in nervous development disorders usually lead to inactivation of this gene. In human tumors, both chromosomal deletion and translocation may also inactivate this gene and consequently contribute to tumorigenesis. Further genetic and cellular functional studies are required to establish its tumor suppressor role.
染色体区域6q的缺失在几种人类癌症中普遍存在,尽管位于该基因组区域内的肿瘤抑制基因(TSGs)尚未完全明确。我们最近的研究在前列腺癌中检测到钠钾转运ATP酶相互作用蛋白2(NKAIN2)基因反复出现染色体截断,在白血病和淋巴瘤中也发现该基因被截断,这表明NKAIN2可能是人类癌症中位于6q常见缺失区域的肿瘤抑制基因之一。NKAIN2基因由八个编码外显子组成,跨越6号染色体q上约1 Mb的基因组DNA,有四种主要的剪接变体。该基因的功能尚未得到充分研究,目前对该基因的了解有限,主要集中在神经系统发育方面。神经发育障碍中的染色体易位通常会导致该基因失活。在人类肿瘤中,染色体缺失和易位也可能使该基因失活,从而促进肿瘤发生。需要进一步的遗传和细胞功能研究来确定其肿瘤抑制作用。