Kanthan Rani, Senger Jenna-Lynn, Kanthan Selliah Chandra
Department of Pathology and Laboratory Medicine, University of Saskatchewan, Saskatoon, SK, Canada S7N 0W8 ; Royal University Hospital, Room 2868 G-Wing, 103 Hospital Drive, Saskatoon, SK, Canada S7N 0W8.
Patholog Res Int. 2012;2012:597497. doi: 10.1155/2012/597497. Epub 2012 May 9.
Colorectal cancer (CRC) is a heterogeneous disease, developing through a multipathway sequence of events guided by clonal selections. Pathways included in the development of CRC may be broadly categorized into (a) genomic instability, including chromosomal instability (CIN), microsatellite instability (MSI), and CpG island methylator phenotype (CIMP), (b) genomic mutations including suppression of tumour suppressor genes and activation of tumour oncogenes, (c) microRNA, and (d) epigenetic changes. As cancer becomes more advanced, invasion and metastases are facilitated through the epithelial-mesenchymal transition (EMT), with additional genetic alterations. Despite ongoing identification of genetic and epigenetic markers and the understanding of alternative pathways involved in the development and progression of this disease, CRC remains the second highest cause of malignancy-related mortality in Canada. The molecular events that underlie the tumorigenesis of primary and metastatic colorectal carcinoma are detailed in this manuscript.
结直肠癌(CRC)是一种异质性疾病,通过由克隆选择引导的多途径事件序列发展而来。CRC发展过程中涉及的途径可大致分为:(a)基因组不稳定,包括染色体不稳定(CIN)、微卫星不稳定(MSI)和CpG岛甲基化表型(CIMP);(b)基因组突变,包括肿瘤抑制基因的抑制和肿瘤癌基因的激活;(c)微小RNA;以及(d)表观遗传变化。随着癌症进展,上皮-间质转化(EMT)会促进侵袭和转移,并伴有额外的基因改变。尽管不断发现遗传和表观遗传标志物,并对该疾病发生发展过程中涉及的替代途径有所了解,但CRC仍是加拿大恶性肿瘤相关死亡的第二大原因。本文详细阐述了原发性和转移性结直肠癌发生的分子事件。