Research Papers:

LRP5 regulates the expression of STK40, a new potential target in triple-negative breast cancers

Sylvie Maubant, Tania Tahtouh, Amélie Brisson, Virginie Maire, Fariba Némati, Bruno Tesson, Mengliang Ye, Guillem Rigaill, Maïté Noizet, Aurélie Dumont, David Gentien, Bérengère Marty-Prouvost, Leanne de Koning, Sardar Faisal Mahmood, Didier Decaudin, Francisco Cruzalegui, Gordon C. Tucker, Sergio Roman-Roman and Thierry Dubois _

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Oncotarget. 2018; 9:22586-22604. https://doi.org/10.18632/oncotarget.25187

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Sylvie Maubant1,*, Tania Tahtouh1,*, Amélie Brisson1, Virginie Maire1, Fariba Némati2, Bruno Tesson1,3, Mengliang Ye1, Guillem Rigaill4,5, Maïté Noizet1, Aurélie Dumont1, David Gentien6, Bérengère Marty-Prouvost1, Leanne de Koning7, Sardar Faisal Mahmood1, Didier Decaudin2, Francisco Cruzalegui8, Gordon C. Tucker8, Sergio Roman-Roman9 and Thierry Dubois1

1Institut Curie, PSL Research University, Translational Research Department, Breast Cancer Biology Group, Paris, France

2Institut Curie, PSL Research University, Translational Research Department, Preclinical Investigation Laboratory, Paris, France

3Institut Curie, PSL Research University, INSERM U900, Paris, France

4Institute of Plant Sciences Paris-Saclay (IPS2), UMR 9213/UMR 1403, CNRS, INRA, Université Paris-Sud, Université d’Evry, Université Paris-Diderot, Sorbonne Paris-Cité, Orsay, France

5Laboratoire de Mathématiques et Modélisation d’Evry (LaMME), Université d’Evry Val d’Essonne, UMR CNRS 8071, ENSIIE, USC INRA, Évry, France

6Institut Curie, PSL Research University, Translational Research Department, Genomics Platform, Paris, France

7Institut Curie, PSL Research University, Translational Research Department, Reverse-Phase Protein Array Platform, Paris, France

8Oncology Research and Development Unit, Institut de Recherches SERVIER, Croissy-Sur-Seine, France

9Institut Curie, PSL Research University, Translational Research Department, Paris, France

*These authors have contributed equally to this work

Correspondence to:

Thierry Dubois, email: [email protected]

Keywords: triple-negative breast cancer; LRP5; LRP6; STK40; targeted therapy

Received: January 18, 2018     Accepted: April 04, 2018     Published: April 27, 2018


Triple-negative breast cancers (TNBCs) account for a large proportion of breast cancer deaths, due to the high rate of recurrence from residual, resistant tumor cells. New treatments are needed, to bypass chemoresistance and improve survival. The WNT pathway, which is activated in TNBCs, has been identified as an attractive pathway for treatment targeting. We analyzed expression of the WNT coreceptors LRP5 and LRP6 in human breast cancer samples. As previously described, LRP6 was overexpressed in TNBCs. However, we also showed, for the first time, that LRP5 was overexpressed in TNBCs too. The knockdown of LRP5 or LRP6 decreased tumorigenesis in vitro and in vivo, identifying both receptors as potential treatment targets in TNBC. The apoptotic effect of LRP5 knockdown was more robust than that of LRP6 depletion. We analyzed and compared the transcriptomes of cells depleted of LRP5 or LRP6, to identify genes specifically deregulated by LRP5 potentially implicated in cell death. We identified serine/threonine kinase 40 (STK40) as one of two genes specifically downregulated soon after LRP5 depletion. STK40 was found to be overexpressed in TNBCs, relative to other breast cancer subtypes, and in various other tumor types. STK40 depletion decreased cell viability and colony formation, and induced the apoptosis of TNBC cells. In addition, STK40 knockdown impaired growth in an anchorage-independent manner in vitro and slowed tumor growth in vivo. These findings identify the largely uncharacterized putative protein kinase STK40 as a novel candidate treatment target for TNBC.

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