Analyses of the APC and TGF‐β Type II Receptor Genes, and Microsatellite Instability in Mucosal Colorectal Carcinomas

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Abstract
APC and transforming growth factor‐β type II receptor (TGF‐β RII) gene mutations, and microsatcllitc instability have been found in sporadic colorectal carcinomas. To clarify further the early alterations in colorectal carcinogenesis, we investigated these genetic changes in 23 protruding‐ and 24 superficial‐type mucosal colorectal carcinomas. TGF‐β RII gene mutations and microsatellite instability were rarely found in these lesions. Nevertheless, APC was mutated in 16 of the 47 (34.0%) mucosal colorectal carcinomas and was significantly more frequently mutated in protruding‐ (I) and superficial elevated‐type (Ila) (14/32,43.8%) than in other superficial‐type (IIa+IIc, IIb, IIc, and IIc+IIa) (2/ 15,13.3%) mucosal colorectal carcinomas (PAPC gene may be involved from the beginning in the tumorigenesis of many early colorectal carcinomas, particularly of the protruding and superficial elevated types. However, there might be a distinct pathway for other superficial‐type colorectal carcinomas, possibly not involving APC as an initial step of tumorigenesis.