Intrinsic variability in the detection of micrometastases in lymph nodes for re-staging of colorectal cancer: effect of individual markers and tissue samples


Autoria(s): Salto-Tellez, Manuel; Kong, S.L.; Leong, A.P.K.; Koay, E.S.C.
Data(s)

01/06/2003

Resumo

In this study, we investigated whether (a) carcinoembryonic antigen (CEA), cytokeratin-20 (CK-20) and guanylyl cyclase C (GCC) are clinically useful markers for the molecular detection of submicroscopic metastases in colorectal cancer (CRC) and (b) whether overexpression of CEA, CK-20 and GCC can be reliably detected in formalin-fixed, paraffin-embedded tissues as well as frozen lymph nodes. We studied 175 frozen lymph nodes and 158 formalin-fixed, paraffin-embedded lymph nodes from 28 cases of CRC. CEA or CK-20 or GCC-specific polymerase chain reaction (PCR) was carried out on mRNA transcripts extracted from the nodal tissues. Ten out of I I Dukes' B CRC cases had detectable CEA and CK-20 while 6 out of 11 Dukes' B CRC cases had detectable GCC. In general, the difference of re-staged cases when comparing frozen and paraffin-embedded samples was marked; the only statistically significant correlation between frozen and paraffin tissue was for the CEA marker. Our results indicated a high incidence (>50%) of detecting micrometastases in histologically-negative lymph nodes at the molecular level. (C) 2003 Elsevier Science Ltd. All rights reserved.

Identificador

http://pure.qub.ac.uk/portal/en/publications/intrinsic-variability-in-the-detection-of-micrometastases-in-lymph-nodes-for-restaging-of-colorectal-cancer-effect-of-individual-markers-and-tissue-samples(ba777151-e744-4d15-8a46-9f604aad4569).html

http://dx.doi.org/10.1016/S0959-8049(03)00231-4

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Salto-Tellez , M , Kong , S L , Leong , A P K & Koay , E S C 2003 , ' Intrinsic variability in the detection of micrometastases in lymph nodes for re-staging of colorectal cancer: effect of individual markers and tissue samples ' European Journal of Cancer , vol 39 , no. 9 , pp. 1234-1241 . DOI: 10.1016/S0959-8049(03)00231-4

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1300/1306 #Cancer Research #/dk/atira/pure/subjectarea/asjc/2700/2720 #Hematology #/dk/atira/pure/subjectarea/asjc/2700/2730 #Oncology
Tipo

article