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p120-catenin in Metastatic Lobular Breast Cancer

Inactivation of E-cadherin leads to invasive lobular breast cancer (ILC) that metastasizes to the gastro-intestinal tract, lungs and bone marrow, reminiscent of the human condition. An emerging theme in literature is the role p120-catenin (p120) in cancer biology. p120 regulates recycling of E-cadherin and data from our laboratory and others have shown that p120 translocates to the cytosol and nucleus upon loss of E-cadherin. In the cytosol p120 functions as an oncogene regulating Rho signaling (see below) and Kaiso transcriptional repression (see Kaiso page). 

We are unraveling the oncogenic signals that emanate from p120 in the cytosol, and performing genome-wide efforts combined with functional biology to identify p120/Kaiso targets in breast cancer. Based on these findings we are designing novel treatment regimens to target metastatic ILC.

Cytosolic p120 expression marks tumor progression of ILC.

Invasive E-cadherin mutant cells showing cytosol and nuclear p120 (black arrow), versus normal luminal mammary epithelial cells (White arrow).

p120 controls ILC tumor growth and metastasis through Rho and Rock.

Doxycyclin (dox)-inducible Rock1 shRNA-expressing mouse ILC cells were transplanted into the 4th inguinal mammary gland of recipient  mice and tumor volumes were measured longitudinally in the presence or absence of dox.


KAISO. Its Regulation by p120 and Consequences for Tumor Progression

Apart from its classical functions at the cell membrane, p120 can also regulate RhoGTPases when translocated to the cytosol (see p120 in lobular breast cancer page). Furthermore, it can interact with and relieve transcriptional repression of Kaiso, leading to expression of distinct target genes. Although controversy still covers the validity of the small number of targets that have been identified, alleged Kaiso target genes show overlap with Wnt signaling targets. As such it advocates Kaiso in a plethora of multiple developmental en pathological processes, including the regulation of tumor development and metastatic disease. 

E-cadherin mutant cells express nuclear p120

Immunofluorescence (IF) showing human and mouse ILC cells (E-cadherin mutant). In contrast, E-cadherin positive breast cancer cells (E-cadherin wild-type) do not express nuclear p120. Arrow heads depict nuclear p120 expression, size bars are 10┬Ám.

 

We have and are studying how Kaiso regulated gene transcription in cancer in a genome-wide manner. We initially focussed on the regulation of Kaiso by p120, but are also interested in p120-independent transcriptional regulation by Kaiso. We have published on how p120 reliefs Kaiso-dependent transcriptional repression of Wnt11 through its classical Kaiso Binding Sequence (KBS) TCCTGCNA, and the effect this has on tumor malignancy. We have also identified ID2 as a canonical Kaiso target that dampens growth and controls dormancy of anchorage independent ILC ells through direct inhibition of Rb phosphorylation.