Department of Pediatric Oncology/Hematology, Erasmus MC/Sophia Children's Hospital, Rotterdam, The Netherlands.
Leukemia. 2012 Apr;26(4):572-81. doi: 10.1038/leu.2011.330. Epub 2011 Nov 18.
NK-like (NKL) homeobox genes code for transcription factors, which can act as key regulators in fundamental cellular processes. NKL genes have been implicated in divergent types of cancer. In this review, we summarize the involvement of NKL genes in cancer and leukemia in particular. NKL genes can act as tumor-suppressor genes and as oncogenes, depending on tissue type. Aberrant expression of NKL genes is especially common in T-cell acute lymphoblastic leukemia (T-ALL). In T-ALL, 8 NKL genes have been reported to be highly expressed in specific T-ALL subgroups, and in ~30% of cases, high expression is caused by chromosomal rearrangement of 1 of 5 NKL genes. Most of these NKL genes are normally not expressed in T-cell development. We hypothesize that the NKL genes might share a similar downstream effect that promotes leukemogenesis, possibly due to mimicking a NKL gene that has a physiological role in early hematopoietic development, such as HHEX. All eight NKL genes posses a conserved Eh1 repressor motif, which has an important role in regulating downstream targets in hematopoiesis and possibly in leukemogenesis as well. Identification of a potential common leukemogenic NKL downstream pathway will provide a promising subject for future studies.
NK 样(NKL)同源盒基因编码转录因子,可作为基本细胞过程中的关键调节因子。NKL 基因已被牵涉到多种类型的癌症中。在这篇综述中,我们总结了 NKL 基因在癌症,特别是白血病中的作用。NKL 基因可以作为肿瘤抑制基因和癌基因,这取决于组织类型。NKL 基因的异常表达在 T 细胞急性淋巴细胞白血病(T-ALL)中尤为常见。在 T-ALL 中,已经报道了 8 个 NKL 基因在特定的 T-ALL 亚组中高度表达,在大约 30%的病例中,高表达是由 5 个 NKL 基因之一的染色体重排引起的。这些 NKL 基因中的大多数在 T 细胞发育过程中通常不表达。我们假设 NKL 基因可能具有相似的下游效应,促进白血病发生,可能是因为模拟了在早期造血发育中具有生理作用的 NKL 基因,如 HHEX。这 8 个 NKL 基因都具有保守的 Eh1 抑制子基序,该基序在造血和可能的白血病发生中对调节下游靶标具有重要作用。确定潜在的共同致白血病的 NKL 下游途径将为未来的研究提供一个有前途的课题。