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Expression of cyclooxgenase-2 in head and neck squamous cel carcinoma
Oleh:
Reksoprawiro, Sunarto
;
Kipsanang Akemah
;
Hoesin, Faroek
Jenis:
Article from Journal - ilmiah nasional - tidak terakreditasi DIKTI
Dalam koleksi:
Jurnal Ilmu Bedah Indonesia (Indonesian Journal Of Surgery) vol. 34 no. 2 (Apr. 2007)
,
page 54.
Topik:
COX-2 Espression
;
Squamous Cell Carcinoma
;
Head and Neck
Ketersediaan
Perpustakaan FK
Nomor Panggil:
J36.K
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Clnical and Papthological parameters alone are not enough to be used to predict the prognosis of the patients. There are the molecular prognostic factors such as cyclooxygenase-2 (COX-2) expression which should be considered to predict the outcome of cancer patient treatment. The purpose of this study was to determine whether COX-2 was over expressed in head and neck squalmous cell carcinoma (HNSCC). Methods : Thirty patients with HNSCC underwent surgery at Soetomo Hospital Surabaya in the period of 2004-2005 was studied. The paraffin blocks of the primary tumor were examined immunohistochemically for COX-2 expression The COX-2 expression of the specimens was graded based on the intensity of immunostaining as negative (0), weak (1), moderate (2), and strong (3). The COX-2 expression score of each specimen was ascertained as multiplication of immunostaining intensity and percentage of the stained cells. Clinical parameters of the patients were reviewed from the medical records. Results : Twenty-eight (93,3%) of the speciments showed positive COX-2 expression in immunohistochemistry staining. The percentage of the stained cells were 0-95%, and COX-2 expression score varied from 0 to 2.85 with mean of 1.27. There was no significant different between male and female, age under and upper 55 years old, intra-oral and extra-oral tumor in COX-2 expression score. Conclusion : Cyclooxygenase (COX)-2 was expressed in HNSCC (93,7% patients), the expression score was not influenced by gender, age, and location of primary tumor.
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