结直肠癌
中文名称
通路描述
结直肠癌(CRC)是西方国家的第二大癌症相关死亡原因。CRC 源于结肠上皮细胞,这是由于定义的原癌基因和肿瘤抑制基因(TSG)中遗传改变的积累所致。在散发性 CRC 进展中已识别出两种主要的基因组不稳定性机制。第一种,称为染色体不稳定性(CIN),涉及原癌基因(如 K-ras)激活和 TSG(如 p53、DCC/Smad4、APC)失活的系列遗传改变。第二种,称为微卫星不稳定性(MSI),是由于 DNA 错配修复基因 MLH1 和/或 MSH2 的启动子超甲基化导致其失活,以及编码微卫星基因(如转化生长因子受体 II,TGF-RII)和 BAX 的次级突变引起的。遗传综合征具有特定基因(如染色体 5q 上的肿瘤抑制基因 APC 在 FAP 中的突变、错配修复基因在 HNPCC 中的突变)的胚系突变。
英文描述
Colorectal cancer (CRC) is the second largest cause of cancer-related deaths in Western countries. CRC arises from the colorectal epithelium as a result of the accumulation of genetic alterations in defined oncogenes and tumour suppressor genes (TSG). Two major mechanisms of genomic instability have been identified in sporadic CRC progression. The first, known as chromosomal instability (CIN), results from a series of genetic changes that involve the activation of oncogenes such as K-ras and inactivation of TSG such as p53, DCC/Smad4, and APC. The second, known as microsatellite instability (MSI), results from inactivation of the DNA mismatch repair genes MLH1 and/or MSH2 by hypermethylation of their promoter, and secondary mutation of genes with coding microsatellites, such as transforming growth factor receptor II (TGF-RII) and BAX. Hereditary syndromes have germline mutations in specific genes (mutation in the tumour suppressor gene APC on chromosome 5q in FAP, mutated DNA mismatch repair genes in HNPCC).
所含基因
87 个基因
AKT1
AKT2
AKT3
APC
APC2
APPL1
ARAF
AREG
AXIN1
AXIN2
BAD
BAK1
BAX
BBC3
BCL2
BCL2L11
BIRC5
BRAF
CASP3
CASP9
CCND1
CDKN1A
CTNNB1
CYCS
DCC
DDB2
EGF
EGFR
EREG
FOS
GADD45A
GADD45B
GADD45G
GRB2
GSK3B
HRAS
JUN
KRAS
LEF1
MAP2K1
MAP2K2
MAPK1
MAPK10
MAPK3
MAPK8
MAPK9
MLH1
MSH2
MSH3
MSH6
MTOR
MYC
NRAS
P3R3URF-PIK3R3
PIK3CA
PIK3CB
PIK3CD
PIK3R1
PIK3R2
PIK3R3
PMAIP1
POLK
RAC1
RAC2
RAC3
RAF1
RALA
RALB
RALGDS
RHOA
RPS6KB1
RPS6KB2
SMAD2
SMAD3
SMAD4
SOS1
SOS2
TCF7
TCF7L1
TCF7L2
TGFA
TGFB1
TGFB2
TGFB3
TGFBR1
TGFBR2
TP53