Multifocal renal cell carcinoma: Evidence for a common clonal origin

Hideaki Miyake, Hideo Nakamura, Isao Hara, Kazuo Gohji, Soichi Arakawa, Sadao Kamidono, Hideyuki Saya

研究成果: Article査読

30 被引用数 (Scopus)


The reported incidence of satellite tumor lesions in kidneys resected by radical nephrectomy for renal cell carcinoma (RCC) is 7-25%; however, genetic analyses of satellite tumors in comparison with those of main tumor lesions have not been performed well. In the present study, we investigated the incidence of loss of heterozygosity (LOH) at chromosome arms 3p, 6q, 8p, 9p, 9q, and 14q using 18 microsatellite markers in 10 nonpapillary RCCs of 50 mm or less in diameter and the accompanying satellite tumor lesions to evaluate the genetic alterations in main and satellite tumors. LOH was detected in 10, 3, 5, 3, 2, and 3 cases at chromosome arms 3p, 6q, 8p, 9p, 9q, and 14q, respectively. In addition, primary and satellite tumor lesions in 8 of 10 cases exhibited identical patterns of LOH on the 18 loci examined. In the remaining two cases, both main and satellite tumors demonstrated LOH on the common seven and three loci, respectively, whereas for another locus, LOH was observed only in the satellite tumor lesions. The similarity of LOH patterns detected in main and satellite tumor lesions indicates that the presence of satellite tumors might be the result of intrarenal metastasis from the main tumor lesion. These findings strongly suggest that even in case of small nonpapillary RCC, nephron-sparing surgery might carry the risk of failing to prevent postoperative local recurrence due to the incomplete resection of unrecognized satellite tumors with genetic alterations similar to those of the main tumor.

ジャーナルClinical Cancer Research
出版ステータスPublished - 1998 10 1

ASJC Scopus subject areas

  • 腫瘍学
  • 癌研究


「Multifocal renal cell carcinoma: Evidence for a common clonal origin」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。