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[Cancer Research 52, 3099-3102, June 1, 1992]
© 1992 American Association for Cancer Research

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Frequent Loss of Heterozygosity at the DCC Locus in Gastric Cancer1

Shinya Uchino2, Hitoshi Tsuda, Masayuki Noguchi, Jun Yokota, Masaaki Terada, Takao Saito, Michio Kobayashi, Takashi Sugimura and Setsuo Hirohashi3

Pathology Division [S. U., H. T., M. N., S. H.], Genetics Division [M. T., T. Su.], and Section of Study on Cancer Metastasis [J. Y.], National Cancer Center Research Institute, 1-1, Tsukiji 5-chome, Chuo-ku, Tokyo 104, and Department of Surgery I, Oita Medical University, 1-1506, Idaigaoka, Hasama-Machi, Oita Gun, Oita 879-56, [S. U., T. Sa., M. K.], Japan

We examined 28 cases of surgically resected gastric cancer, excluding the diffuse type, for loss of heterozygosity (LOH) on 12 chromosomal arms using polymorphic DNA markers. LOH on chromosome 18q was detected in 61% (14 of 23) of the cases by the probes OLVIIA8, OLVIIE10, p15–65, SAM 1.1, and OS-4, and a putative common region showing LOH included the locus of the DCC tumor suppressor gene. LOH on chromosome 17p was also frequently found (8 of 19 or 42% of the cases) by the probes p10–3 and pHF12–1, and in 5 of these 6 cases the LOH on chromosome 17p was accompanied by LOH on chromosome 18q. On the other hand, the incidence of LOH was 30% or less using probes pHRnES, pHF12–65, p-c-mybE2.6, NJ3 3.2, pHF12–8, pHINS6.0, p9D11, hp2-{alpha}, pCMM6, and P1A5 on chromosomes 1q, 5, 6q, 7q, 9, 11p, 13q, 16q, 20, and 22q, respectively. LOH on chromosome 18q was frequent irrespective of the depth of tumor invasion, whereas the incidence of LOH on chromosome 17p was higher in the cases in which the tumor invaded beyond the muscularis propria than in those in which tumor invasion was limited to the submucosa and muscularis propria.

These results suggest that LOH on chromosome 18q occurs at an earlier stage than LOH on chromosome 17p and that the inactivation of tumor suppressor genes located on chromosome 17p and 18q (e.g., the p53 and DCC genes) is critically involved in the development of the majority of gastric cancers. While alteration of the p53 gene is observed in various human cancers, that of the DCC gene is considered to occur more selectively in gastrointestinal cancers.

1 Supported in part by a Grant-in-Aid from the Ministry of Health and Welfare of Japan for the Comprehensive 10-Year Strategy for Cancer Control.

2 S. U. is a recipient of a Research Resident Fellowship from the Foundation for the Promotion of Cancer Research.

3 To whom reprint requests should be addressed.

Received 10/25/91. Accepted 3/19/92.




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Copyright © 1992 by the American Association for Cancer Research.