The relationship between gastric cancer cells circulating in the blood and microsatellite instability positive gastric carcinomas

被引:9
作者
Czopek, J
Bialas, M
Rudzki, Z
Zazula, M
Pituch-Noworolska, A
Zembala, M
Popiela, T
Kulig, J
Kolodziejczyk, P
Stachura, J
机构
[1] Jagiellonian Univ, Coll Med, Dept Pathol, PL-31531 Krakow, Poland
[2] Jagiellonian Univ, Coll Med, Dept Immunol, PL-31531 Krakow, Poland
[3] Jagiellonian Univ, Coll Med, Dept Surg 1, PL-31531 Krakow, Poland
关键词
D O I
10.1046/j.1365-2036.16.s2.5.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Cancers characterized by microsatellite instability may be biologically different from their counterparts with stable microsatellite sequences. Circulating cancers cell present in blood prior to surgery may constitute an adverse prognostic finding. Aim: To correlate these two phenomena with morphological features and survival in advanced gastric cancer. Methods: We examined 76 cases of resected sporadic, advanced gastric cancer by means of routine morphology and a panel of microsatellite markers. Sixty-six cases were screened for presence of cancer cells circulating in blood prior to the surgery using combined morphological and immunocytochemical approach. Results: Twenty-one (27.6%) cases demonstrated microsatellite instability in at least one locus. Among them 11 (14.5%) showed microsatellite instability in more than 30% (4/12) examined loci, and they were therefore designated as replication error positive (RER+). Circulating cancer cells were detected in 2/19 microsatellite instability and in 11/47 remaining cases (difference not significant). The survival of the microsatellite instability cases was significantly better. The presence of circulating cancer cells did not correlate with survival. Conclusion: It is possible that the microsatellite instability status, but not circulating cancer cells, constitutes a prognostic predictive factor in advanced gastric carcinoma. Confirmation of this hypothesis requires continuation of patient follow-up.
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页码:128 / 136
页数:9
相关论文
共 32 条
[1]   Genetic predisposition to gastric cancer [J].
Bevan, S ;
Houlston, RS .
QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS, 1999, 92 (01) :5-10
[2]  
BOCKER T, 1999, BIOCHIM BIOPHYS ACTA, V1423, P1
[3]  
Boland CR, 1998, CANCER RES, V58, P5248
[4]  
Caldas C, 1999, J MED GENET, V36, P873
[5]   Evidence of genetic progression in human gastric carcinomas with microsatellite instability [J].
Chung, YJ ;
Park, SW ;
Song, JM ;
Lee, KY ;
Seo, EJ ;
Choi, SW ;
Rhyu, MG .
ONCOGENE, 1997, 15 (14) :1719-1726
[6]   Microsatellite instability at multiple loci in gastric carcinoma: Clinicopathologic implications and prognosis [J].
DosSantos, NR ;
Seruca, R ;
Constancia, M ;
Seixas, M ;
SobrinhoSimoes, M .
GASTROENTEROLOGY, 1996, 110 (01) :38-44
[7]   Infrequent loss of heterozygosity of APC MCC and DCC genes in gastric cancer showing DNA microsatellite instability [J].
Fang, DC ;
Jass, JR ;
Wang, DX ;
Zhou, XD ;
Luo, YH ;
Young, J .
JOURNAL OF CLINICAL PATHOLOGY, 1999, 52 (07) :504-508
[8]   Microsatellite instability is an independent indicator of recurrence in sporadic stage I-II endometrial adenocarcinoma [J].
Fiumicino, S ;
Ercoli, A ;
Ferrandina, G ;
Hess, P ;
Raspaglio, G ;
Genuardi, M ;
Rovella, V ;
Bellacosa, A ;
Cicchillitti, L ;
Mancuso, S ;
Bignami, M ;
Scambia, G .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (04) :1008-1014
[9]   MEDICAL PROGRESS - GASTRIC-CARCINOMA [J].
FUCHS, CS ;
MAYER, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (01) :32-41
[10]   DIFFERENCES IN THE MODE OF THE EXTENSION OF GASTRIC-CANCER CLASSIFIED BY HISTOLOGICAL TYPE - NEW HISTOLOGICAL CLASSIFICATION OF GASTRIC-CARCINOMA [J].
GOSEKI, N ;
TAKIZAWA, T ;
KOIKE, M .
GUT, 1992, 33 (05) :606-612