Sa. Waldman et al., USE OF GUANYLYL CYCLASE-C FOR DETECTING MICROMETASTASES IN LYMPH-NODES OF PATIENTS WITH COLON-CANCER, Diseases of the colon & rectum, 41(3), 1998, pp. 310-315
INTRODUCTION: Guanylyl cyclase C appears to be expressed only in color
ectal cancer cells in extraintestinal tissues. Thus, guanylyl cyclase
C may be useful as a marker to detect colorectal cancer micrometastase
s not detectable by histopathology in lymph nodes of patients. METHODS
: Twelve patients with colon adenocarcinoma, Dukes Stages A through C2
, and one patient with a tubulovillous adenoma were included in this s
tudy. Forty-two lymph nodes were collected from fresh surgical specime
ns, and each was examined by histopathology and reverse transcription
followed by polymerase chain reaction using guanylyl cyclase C-specifi
c primers. Histopathology identified colon cancer cells in 6 of 16 lym
ph nodes from five Dukes Stage C patients but not in lymph nodes from
the patient with a tubulovillous adenoma, the Dukes Stage A patient, o
r six Dukes Stage B patients. Reverse transcription followed by polyme
rase chain reaction using guanylyl cyclase C-specific primers was perf
ormed on all 42 lymph nodes. RESULTS: Guanylyl cyclase C messenger RNA
was not detected by reverse transcription followed by polymerase chai
n reaction in lymph nodes from the patient with the tubulovillous aden
oma or the patient with Dukes Stage A colon carcinoma. Seven lymph nod
es from Dukes Stage C patients revealed guanylyl cyclase C messenger R
NA including six lymph nodes containing histopathologically confirmed
metastases. Of significance, guanylyl cyclase C messenger RNA. was det
ected in 4 of 21 lymph nodes from Dukes Stage B patients. Indeed, clin
ical staging of two patients could be upgraded from B to C using rever
se transcription followed by polymerase chain reaction and guanylyl cy
clase C-specific primers. CONCLUSION: Reverse transcription followed b
y polymerase chain reaction using guanylyl cyclase C-specific primers
might be useful to more accurately assess micrometastases in lymph nod
es of colorectal cancer patients undergoing disease staging.