Immunohistochemical analysis of Ki-67, p21waf1/cip1 and apoptosis in marker lesions from patients with superficial bladder tumours treated with vinorelbine intravesical therapy in a preliminary phase I trial
Autor: | R.D. Bonfil, L. Metz, F. Mosso, F.D. Cuello Carrion, E. Fayad, Daniel R. Ciocca, M. Reale, A. Villaronga, A.J. Schmilovich, D. Siguelboim, A.D. Gonzalez |
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Rok vydání: | 2001 |
Předmět: |
Pathology
medicine.medical_specialty Chemotherapy Urinary bladder medicine.diagnostic_test biology business.industry Urology medicine.medical_treatment Phases of clinical research Vinorelbine medicine.disease Vinblastine medicine.anatomical_structure Ki-67 Biopsy biology.protein Carcinoma Medicine business medicine.drug |
Zdroj: | BJU International. 88:425-431 |
ISSN: | 1464-4096 |
DOI: | 10.1046/j.1464-410x.2001.02340.x |
Popis: | Objective To investigate Ki-67 and p21Waf1/Cip1 expression and apoptosis, before and after treatment, in tumour biopsies obtained from patients with superficial bladder cancer who underwent vinorelbine intravesical therapy. Patients and methods Twenty patients with high-risk superficial bladder cancer (including one or more of the following parameters: tumour diameter > 3 cm, histological grade 3, or multicentric tumours) were treated 1–6 times (weekly) with intravesical vinorelbine (50 mg/mL) instillations. Transurethral tumour marker biopsies were obtained one week before the first instillation of the drug and one week after the last. The biopsies were immunostained for Ki-67 and p21Waf1/Cip1 with monoclonal antibodies, on tissue sections derived from paraffin-embedded samples obtained before and after vinorelbine treatments. In addition, apoptosis was determined using a terminal deoxynucleotidyl transferase-mediated dUTP biotin nick-end labelling (TUNEL) technique. Results There were no significant differences in the cell proliferation marker Ki-67 in biopsies taken before or after treatment. However, p21Waf1/Cip1 showed significantly higher expression in biopsies obtained after vinorelbine treatment, with median (range) values of 40 (20–90)% before and 70 (50–80)% after (P |
Databáze: | OpenAIRE |
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