Ab. Tuck et al., OSTEOPONTIN AND P53 EXPRESSION ARE ASSOCIATED WITH TUMOR PROGRESSION IN A CASE OF SYNCHRONOUS, BILATERAL, INVASIVE MAMMARY CARCINOMAS, Archives of pathology and laboratory medicine, 121(6), 1997, pp. 578-584
Citations number
40
Categorie Soggetti
Pathology,"Medical Laboratory Technology","Medicine, Research & Experimental
Objective.-To examine the association between expression of osteoponti
n (OPN), p53, other molecular markers (Ki-67, c-erb B2, and estrogen r
eceptor protein) and tumor progression in a case of synchronous, bilat
eral, invasive mammary carcinomas of the same histology. Design.-Immun
ohistochemistry was performed on formalin-fixed, paraffin-embedded tis
sue sections. Plasma OPN level was determined by a quantitative antige
n capture assay. Setting.-The patient was seen, treated, and followed
up for a period of 5 years at the London Regional Cancer Centre, Ontar
io, Canada. Patient.-A 60-year-old woman presented with bilateral infi
ltrating mammary carcinomas of the same histologic type and grade. Bil
ateral mastectomy and axillary node dissection showed involvement of 3
of 12 right axillary and 0 of 11 left axillary lymph nodes. She later
developed a right chest wall recurrence, followed by widespread metas
tatic disease to the skull, liver, and left femur Results.-The primary
tumor of the right breast was OPN-and p53-positive, whereas the tumor
of the left breast was negative for both markers. The development of
right axillary lymph node metastases, chest wall recurrence, and dista
nt metastases was associated in all instances with an immunohistochemi
cal profile of high level expression of OPN and p53. Plasma assay for
OPN at the time of last admission showed a markedly elevated OPN level
. Conclusions.-lncreased p53 expression was found to be associated wit
h increased tumor aggressiveness, The association of increased OPN exp
ression with increased malignancy in breast cancer is a novel finding
and raises the possibility of a role for OPN in tumor progression, as
well as the potential for this marker in predicting clinical aggressiv
eness.