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Survivin and Ki67 proliferative index in breast carcinoma (CROSBI ID 309263)

Prilog u časopisu | izvorni znanstveni rad | domaća recenzija

Veliki Dalić, Irena ; Milković Periša, Marija ; Šarčević, Božena Survivin and Ki67 proliferative index in breast carcinoma // Libri oncologici : Croatian journal of oncology, 44 (2016), 2-3; 1-6

Podaci o odgovornosti

Veliki Dalić, Irena ; Milković Periša, Marija ; Šarčević, Božena

engleski

Survivin and Ki67 proliferative index in breast carcinoma

Survivin is a member of the inhibitor of apoptosis (IAP) family. It is also involved in the regulation of cell division.Survivin is widely expressed in foetal tissues and in human cancers, but generally not in normal adult tissue. This study examined the expression of survivin protein in a series of 50 cases of invasive primary breast carcinoma. Our study comprised 50 cases of breast cancer, 10 of each immunophenotype. All tumours were diagnosed as invasive ductal carcinoma (Not Otherwise Specifi ed, NOS). Formalin-fi xed, paraffi n-embedded tissue sections were immunostained for survivin. Survivin immunoreactivity was evaluated as follows: 0(0-5% positive cells) ; 1(5–20%) ; 2(21–50%) ; 3(51– 75%) ; 4(>76%) with cutoff value of 20% that was established as a positive result. Immunohistochemical analysis showed positive expression for survivin in 18 of 50 cases (36%) of breast carcinomas of TNM stages I to III. In previous studies, there was significant relationship between survivin expression and negative prognostic factors like larger tumour size, higher histologic grade and negative hormonal status. What we should emphasize in our study is the correlation between HER2 positive tumours and survivin expression (P=0.007) and strong association of survivin expression in cytoplasm in HER2 positive tumours as a predictor of unfavourable outcome. Further larger studies are needed in future to explore and explain the facts about survivin and its connection with breast cancer.

apoptosis ; survivin ; breast cancer

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Podaci o izdanju

44 (2-3)

2016.

1-6

objavljeno

2584-3826

Povezanost rada

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