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DOI 10.1700/1430.15820

Медицинская библиотека · Tumori · 2014

Topoisomerase II alpha and microtubule-associated protein-tau as a predictive marker in axillary lymph node positive breast cancer.

Won Hye Sung, Lee Kyoung Eun, Sung Sun Hee, Choi Moon Young, Jo Jung Youn, Nam Eun Mi, Mun Yeung-Chul, Seong Chu-Myong, Lee Soon Nam

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Аннотация

AIMS AND

BACKGROUND

The aims of this study were to investigate the correlation between topoisomerase II alpha (TOP2A), microtubule-associated protein-tau (MAP-tau) and other prognostic factors in breast cancer and to evaluate the predictive value of TOP2A and MAP-tau in breast cancer patients who received anthracycline and taxane-containing adjuvant chemotherapy.

METHODS AND STUDY

DESIGN

Seventy patients with axillary lymph node positive breast cancer who underwent curative surgery between January 2000 and December 2005 were evaluated retrospectively. The levels of protein expression of TOP2A and MAP-tau were assessed using immunohistochemistry.

RESULTS

Among the 70 patients, 43 (61.4%) showed TOP2A overexpression and 30 (42.9%) showed MAP-tau positivity. TOP2A overexpression was associated with p53 positivity and high histological grade. MAP-tau positivity was associated with a lower positive lymph node ratio, lower proliferative activity, and hormone receptor positivity. Based on the TOP2A and MAP-tau expression, there was no significant difference in disease-free survival in the breast cancer patients who received anthracycline and taxane-containing adjuvant chemotherapy.

CONCLUSIONS

We conclude that immunohistochemical analysis of TOP2A and MAP-tau protein expression may not predict the benefits of adjuvant anthracycline and taxane chemotherapy in axillary node positive breast cancer.

Для цитирования: Won Hye Sung, Lee Kyoung Eun, Sung Sun Hee, Choi Moon Young, Jo Jung Youn, Nam Eun Mi, Mun Yeung-Chul, Seong Chu-Myong, Lee Soon Nam. Topoisomerase II alpha and microtubule-associated protein-tau as a predictive marker in axillary lymph node positive breast cancer.. Tumori. 2014. DOI: 10.1700/1430.15820.

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