IMMUNOHISTOCHEMICAL EXPRESSION OF MELK IN BREAST CANCER Manieli C*, Saccani S*, Lai ML*, Pilloni L*,...

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IMMUNOHISTOCHEMICAL EXPRESSION OF MELK IN BREAST CANCER Manieli C*, Saccani S*, Lai ML*, Pilloni L*, Coni PP*, Senes G*, Faa G*, Van den Oord JJ°. *I Cattedra Anatomia Patologica, University of Cagliari, Italy. °University Hospitals, Katholieke Universiteit Leuven, Belgium.

Transcript of IMMUNOHISTOCHEMICAL EXPRESSION OF MELK IN BREAST CANCER Manieli C*, Saccani S*, Lai ML*, Pilloni L*,...

Page 1: IMMUNOHISTOCHEMICAL EXPRESSION OF MELK IN BREAST CANCER Manieli C*, Saccani S*, Lai ML*, Pilloni L*, Coni PP*, Senes G*, Faa G*, Van den Oord JJ°. *I Cattedra.

IMMUNOHISTOCHEMICAL EXPRESSION OF MELK IN

BREAST CANCER

Manieli C*, Saccani S*, Lai ML*, Pilloni L*, Coni PP*, Senes G*, Faa G*, Van den Oord JJ°.*I Cattedra Anatomia Patologica, University of Cagliari, Italy.°University Hospitals, Katholieke Universiteit Leuven, Belgium.

Page 2: IMMUNOHISTOCHEMICAL EXPRESSION OF MELK IN BREAST CANCER Manieli C*, Saccani S*, Lai ML*, Pilloni L*, Coni PP*, Senes G*, Faa G*, Van den Oord JJ°. *I Cattedra.

Background (1)

• MELK (Maternal Embryonic Leucine Zipper Kinase) is a member of the snf1/AMPK family of serine-threonine kinases;

• Its specific targets in normal cells have not been identified yet, and its role is therefore still elusive.

• However, several studies reported an increased expression of MELK in various tumours compared to normal tissues.

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Background (2)In breast cancer cell lines and in breast tumours an

elevated expression of MELK was found by semi-quantitative RT-PCR and by Western Blot analysis; MELK, by interaction with and phosphorylation of Bcl-G, a pro-apoptotic member of the Bcl-2 family, has an anti-apoptotic effect on tumour cells growth in vitro. Meng-Lay Lin et al, Breast Cancer Research 2007,9:R17.

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The aim of the present study was to assess the expression of MELK by immunohistochemistry, comparing normal mammary tissue and breast tumours.

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Design

Immunohistochemical studies were performed on frozen sections from 17 consecutive cases of breast cancer and 4 cases of normal mammary gland, using a mouse monoclonal antibody against Melk. Immunostaining was also performed for Estrogen (ER) and Progesteron (PR) Receptors and Cerb-B2.

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Results (1)

• MELK was not expressed in normal mammary gland • 7 out of 17 breast tumours examined showed

immunoreactivity for MELK.

Normal mammary gland

Invasive ductal carcinoma (IDC).

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• A cytoplasmatic staining was present in all 7 cases; 5 cases showed both cytoplasmatic and nuclear stain.

• All Melk positive tumours were ER and PR positive and Cerb-B2 negative.

Results (2)

Invasive ductal carcinoma (IDC).

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Conclusions

Our data show that MELK is expressed by cancer cells in a subgroup of breast tumours.

In addition, MELK expression was associated with estrogen and progesteron receptor immunoreactivity.

The issue of whether MELK immunostaining may have a prognostic significance in breast cancer needs further studies.