Expression of the deleted in colorectal cancer gene is related to prognosis in DNA diploid and low proliferative colorectal adenocarcinoma

Citation
Xf. Sun et al., Expression of the deleted in colorectal cancer gene is related to prognosis in DNA diploid and low proliferative colorectal adenocarcinoma, J CL ONCOL, 17(6), 1999, pp. 1745-1750
Citations number
28
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
JOURNAL OF CLINICAL ONCOLOGY
ISSN journal
0732183X → ACNP
Volume
17
Issue
6
Year of publication
1999
Pages
1745 - 1750
Database
ISI
SICI code
0732-183X(199906)17:6<1745:EOTDIC>2.0.ZU;2-X
Abstract
Purpose: Whether or not the deleted in colorectal cancer (DCC) gene is impl icated in metastases or in predicting prognosis in patients with colorectal cancer has not previously been substantiated. Our aims were to investigate DCC expression in primary colorectal cancers and in metastases to identify any prognostic significance. Patients and Methods: DCC expression was examined immunohistochemically in 195 primary colorectal adenocarcinomas and in 23 paired primary tumors and lymph node metastases. DNA content and S-phase fraction were measured by fl ow cytometry. Results: The absence of DCC expression was observed in 55 primary tumors (2 8%), DCC negativity was significantly related to poor prognosis in patients with DNA diploid tumors (P = .03) and chose with a low S-phase fraction (< 5%, P = .02) but not in patients with nondiploid tumors or those with a hi gher S-phase fraction. Furthermore, DCC expression retained its prognostic significance in the diploid subgroup after adjusting for sex, age, site, st age, growth pattern, and differentiation (P = .01). DCC expression was simi lar in primary tumors and their metastases. Conclusion: The absence of DCC predicted a poor outcome in the patients wit h diploid tumors and chose tumors with a low S-phase fraction. Immunohistoc hemistry may be considered as a practical test to assess prognosis in this subgroup of patients. (C) 1999 by American Society of Clinical Oncology.