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. 1999 Dec;90(12):1321–1328. doi: 10.1111/j.1349-7006.1999.tb00715.x

C‐kit Gene Abnormalities in Gastrointestinal Stromal Tumors (Tumors of Interstitial Cells of Cajal)

Shinji Sakurai 1,✉, Tomoki Fukasawa 1,✉, Ja‐Mun Chong 1,✉, Akira Tanaka 1,✉, Masashi Fukayama 1,✉
PMCID: PMC5926026  PMID: 10665649

Abstract

Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the GI tract, and expresses KIT and CD34 in most cases. Gain‐of‐function mutation of the c‐kit proto‐oncogene has been described, but its significance in GIST has not yet been fully evaluated. Mutation in exon 11 of the c‐kit gene was determined by both polymerase chain reaction‐single strand conformation polymorphism (PCR‐SSCP) analysis and direct sequencing in primary and metastatic GISTs and esophageal leiomyomas in Japanese subjects. C‐kit gene mutation was identified in 15 of 48 primary GISTs (31%), four of seven metastatic GISTs, but none of the leiomyomas. Three mutations were mis‐sense point mutations, and 16 were in‐frame deletions of 3–48 bp. C‐kit gene mutation was observed equally in low‐ and high‐risk groups, and was not related to any clinical and pathologic factors, phenotypes or Ki‐67 labeling index (LI) of tumor cells. In five of 15 deletion mutations (four in primary tumors and one in a metastatic tumor), the mutations were present at the distal location of exon 11 of the c‐kit gene, which was a minor mutation in previous reports from Finland and the USA. C‐kit gene mutations in GIST are not always related to a poor prognosis, but further comparative studies are necessary in Western and Japanese populations.

Keywords: C‐kit, Mutation, GIST

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