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Serrated colorectal cancer: Molecular classification, prognosis, and response to chemotherapy
被引:34
|作者:
Murcia, Oscar
[1
]
Juarez, Miriam
[1
]
Hernandez-Illan, Eva
[1
]
Egoavil, Cecilia
[1
]
Giner-Calabuig, Mar
[1
]
Rodriguez-Soler, Maria
[1
]
Jover, Rodrigo
[1
]
机构:
[1] Hosp Gen Univ Alicante, Unidad Gastroenterol, Inst Invest Sanitaria Isabial, 12 Pintor Baeza, Alicante 03010, Spain
关键词:
Colorectal cancer;
Methylator phenotype;
Serrated pathway;
Chemotherapy;
CIMP;
ISLAND METHYLATOR PHENOTYPE;
III COLON-CANCER;
CETUXIMAB PLUS IRINOTECAN;
BRAF MUTATION STATUS;
MICROSATELLITE-INSTABILITY;
DNA METHYLATION;
MISMATCH REPAIR;
1ST-LINE TREATMENT;
ADJUVANT CHEMOTHERAPY;
HYPERPLASTIC POLYPS;
D O I:
10.3748/wjg.v22.i13.3516
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Molecular advances support the existence of an alternative pathway of colorectal carcinogenesis that is based on the hypermethylation of specific DNA regions that silences tumor suppressor genes. This alternative pathway has been called the serrated pathway due to the serrated appearance of tumors in histological analysis. New classifications for colorectal cancer (CRC) were proposed recently based on genetic profiles that show four types of molecular alterations: BRAF gene mutations, KRAS gene mutations, microsatellite instability, and hypermethylation of CpG islands. This review summarizes what is known about the serrated pathway of CRC, including CRC molecular and clinical features, prognosis, and response to chemotherapy.
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页码:3516 / 3530
页数:15
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