Mercia M. Pacheco
University of São Paulo
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Clinical & Experimental Metastasis | 1998
Mercia M. Pacheco; Mário Mourão; Edson B. Mantovani; Inês Nobuko Nishimoto; M. Mitzi Brentani
The purpose of this study was to investigate the association among matrix metalloproteinases (gelatinases A and B, stromelysin-3 (ST3) and matrilysin) mRNAs expressed in primary breast carcinomas and stan-dard prognostic parameters and clinical outcome. mRNA levels were determined by Northern analysis in samples of 81 breast cancer patients (median follow-up, 40 months) and 27 samples of uninvolved adjacent breast tissue. Proteases were expressed by the majority of the tumors and normal breast tissues examined. ST3, gelatinase A and matrilysin mRNAs were more often expressed at high levels in carcinomatous than in normal breast tissues. Differences in the distribution of gelatinase B mRNA were not found. However, paired normal tissues generally produced weaker signals when compared to matched tumor samples. Univariate analysis showed no significant association of gelatinase A and matrilysin mRNAs with the classical prognostic markers (age, menopausal status, stage, size, nodal status, vascular infiltrate, necrosis, steroid receptors, metastasis and survival). Overexpression of ST3 was more frequently found in tumors of post-menopausal women (P < 0.022). Elevated expression of gel B mRNA was associated with the presence of vascular infiltrate (P < 0.026), necrosis (P < 0.039), PR negative tumors (P < 0.014) and inversely corre-lated to the number of survivors (P < 0.021). Multivariate analysis including 68 patients for whom all information was available indicated that neither stromelysin correlated significantly with pathological, clin-ical or biochemical features. High levels of gelatinase A and B mRNAs were inversely associated with the number of survivors. Our findings suggest that measurements of gelatinase A and B mRNAs expression in breast carcinoma may help to identify patients with an agressive form of the disease. ©Lippincott Williams & Wilkins
Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2002
Mercia M. Pacheco; L.P. Kowalski; Inês Nobuko Nishimoto; Maria Mitzi Brentani
Head and neck squamous cell carcinomas (HNSCC) are known for their invasive behavior. The invasiveness of these tumors requires proteases, some of which as urokinase‐type plasminogen activator (uPA), gelatinase B and matrilysin are regulated through AP‐1 dependent transcriptional mechanisms. AP‐1 consists of several proteins, including those encoded by the proto‐oncogenes c‐jun and c‐fos. The aim of this study was to: first, evaluate the expression levels of matrix metalloproteases (matrilysin and gelatinase B) and uPA mRNAs; second, examine whether these genes might be associated with c‐jun and c‐fos expression; third, examine the relationship between the expression of these genes and HNSCC clinico‐pathological features.
Chest | 1984
M. Mitzi Brentani; Carlos Roberto Ribeiro de Carvalho; Paulo Hilário Nascimento Saldiva; Mercia M. Pacheco; C.T.F. Oshima
Genes, Chromosomes and Cancer | 1994
Maria A. Nagai; Lidia Yamamoto; Sibeli Salaorni; Mercia M. Pacheco; M. Mitzi Brentani; Edson Mantovani Barbosa; Ricardo R. Brentani; Sylvie Mazoyer; Simon A. Smith; Bruce A.J. Ponder; Lois M. Mulligan
Clinical Cancer Research | 2000
Anne Hansen Ree; Mercia M. Pacheco; Marianne Tvermyr; Øystein Fodstad; M. Mitzi Brentani
International Journal of Cancer | 1986
Maria Mitzi Brentani; Eduardo L. Franco; Celina Tizuko F. Oshima; Mercia M. Pacheco
Anticancer Research | 1986
Mercia M. Pacheco; Celina Tizuko F. Oshima; M. P. Lopes; A. Widman; Eduardo L. Franco; M. Mitzi Brentani
British Journal of Cancer | 1994
M. A. Nagai; Mercia M. Pacheco; M. M. Brentani; Lourdes A. Marques; R. R. Brentani; B A J Ponder; Lois M. Mulligan
International Journal of Cancer | 1988
Mercia M. Pacheco; M. Mitzi Brentani; Eduardo L. Franco; Jose A. Fontelles; Dalton de Alencar Fischer Chamone; Lourdes A. Marques
Chest | 1985
Paulo Hïlário Nascimento Saidiva; Maria Mitzi Brentani; Carlos Roberto Ribeiro de Carvalho; José Otávio; Costa Auler; Débora Fernandes Calheiros; Mercia M. Pacheco