High expression of PTPN21 in B-cell non-Hodgkin's gastric lymphoma, a positive mediator of STAT5 activity

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Citation: Blood Cancer Journal (2016) 6, e388; doi:http://dx.doi.org/10.1038/bcj.2015.107

Web End =10.1038/bcj.2015.107 http://www.nature.com/bcj

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LETTER TO THE EDITOR

High expression of PTPN21 in B-cell non-Hodgkins gastric lymphoma, a positive mediator of STAT5 activity

Blood Cancer Journal (2016) 6, e388; doi:http://dx.doi.org/10.1038/bcj.2015.107

Web End =10.1038/bcj.2015.107 ; published online 15 January 2016

Investigations of specic pathologic mechanisms of a disease often provide extraordinary opportunities to identify suitable diagnostic markers and alternative treatment options. We investigated whether altered protein tyrosine phosphatase (PTP) activity might be linked to the development of stomach cancer, which is the most common gastrointestinal malignancy and the third leading cause of cancer-related death worldwide.1

Perturbations of PTP activity caused by mutations and manifested as PTP overexpression result in malignant transformation. Thus, PTPs might serve as alternative diagnostic markers and anticancer targets. Here, we report an uncommon phosphatase, PTP non-receptor 21 (PTPN21), which in recent years has been suspected of playing a pathologic role in gastrointestinal tract tumorigenesis. A previous mutational analysis of the PTP gene superfamily identied PTPN21 as having the highest mutation frequency in types of colon cancer with microsatellite instability,2 and a later study found that PTPN21 affects mitogenic signaling in bladder cancer.3 Coincidentally, a systematic expression proling study of 87 PTPs4 and an independent oligonucleotide microarray study,5 identied 22 PTPs (including PTPN21)4 and PTPN21,5 respectively, both studies illustrated distinctly different expression patterns of PTPN21 in gastric carcinoma and normal gastric tissue.

Our analysis of PTPN21 expression in samples of stomach tissue obtained from 56 individuals revealed low to medium expression of PTPN21 in samples of human gastric non-carcinoma tissue (n = 10; Figure 1a), as well as samples of TNM Classication of Malignant Tumors stage I (n = 4), II (n = 10) and III (n = 23) human gastric adenocarcinoma tissue. A subgroup analysis of human stage I gastric carcinoma tissue revealed that PTPN21 expression was signicantly associated with cytosolic E-cadherin expression (r = 0.40; P-valueo0.001; Supplementary Figure S1 and

Supplementary Methods and Materials). On a proportional scale, this suggested an association between PTPN21 and E-cadherin intensities (r = 0.24; P-valueo0.07). A 2-test revealed a signicant correlation (P-value = 0.01) between PTPN21 levels and the expression scores for cytosolic E-cadherin, suggesting an inverse relationship between the expression patterns of membrane E-cadherin and PTPN21. However, overall PTPN21 is often expressed at moderate, but largely uniform, levels in virtually all noncancerous gastric tissues.

Physiologically, PTPN21 directly dephosphorylates ErbB1 and ErbB4 (members of the receptor tyrosine kinase family),3,6 resulting in upregulation of its downstream signaling. In turn, this results in the constitutive activation of Src and increases the activity of ETS domain-containing protein (Elk-1) via regulation of the MEK-Elk-1 signaling pathway.7 However, not much is known about PTPN21 and its alternative ErbB4-dependent downstream targets. Hence, the present study extends our previous work, which demonstrated that PTPN21 controls the accumulation of ErbB4 in human embryonic kidney cells and mouse embryonic cortical neurons.6 In the present study, reciprocal immunoprecipitation conrmed that PTPN21 interacts with ErbB4 in SGC 7901

gastric cancer cells (Supplementary Figure S2 and Supplementary Methods and Materials) in a manner previously described.6

Moreover, ErbB4 is a receptor that is directly upstream of STAT5,8 and STAT5 activation mediates a wide variety of activities induced by growth factors, cytokines and interferons. For example, STAT5 is activated by epidermal growth factor (EGF), which induces translocation of STAT5 into the nucleus and is highly expressed in both lymphoma cell lines and clinical samples of human lymphoma gastrointestinal tissue.9 In addition, STAT5 binds to the gamma-interferon activation motif within the promoter region of STAT5 target genes to activate transcription of the pro-survival genes, -casein and Cyclin D1.10 Such ndings suggest that PTPN21 expression can induce higher than normal levels of STAT5 activity in both human B-cell lymphoma and gastric cells.

To examine the functional consequences of the suggested association between PTPN21 and STAT5, we analyzed the effect of PTPN21 on the STAT5 target gene -casein. PTPN21 promoted dose-dependent increases (up to 3.1 0.32-fold) in the transcription of -casein, and this induction was further enhanced5.2 0.43-fold by co-expression of ErbB4 with PTPN21 (Figure 1b and Supplementary Methods and Materials) in a STAT5A-specic manner (Figure 1c). Immunoreactivity assays showed that in SGC 7901 cells, STAT5 levels increased with binding activity in a PTPN21-dependent manner (Figures 1d and e). The ErbB receptor antagonist AG1478 blocked all PTPN21-dependent -casein transcription, suggesting that the effect of PTPN21 on -casein is dependent on the ErbB4 receptor.

Unexpectedly, PTPN21 failed to enhance -casein translation, even following EGF stimulation. This discrepancy in translation of Cyclin D1 and -casein may be due to differences in the availability of specic coactivators required to assemble the transcriptional coactivator complexes (TCC) for either protein. For example, it is important to note that STAT5 interacts with Oct1 to form a TCC needed to promote Cyclin D1 transcription.10 In addition, STAT5 must also bind to nuclear receptor coactivator 1 (NCOA1) and the glucocorticoid receptor (GR) to form a TCC that promotes -Casein transcription.11 This suggests that the -casein transcription rates are also dependent on the formation of a transcription factor complex with NCOA1 and GR; the transcription reporter assay used in this study accurately reected the signicance of PTPN21-dependent STAT5 activation.

Ligand stimulation in HEK 293 cells overexpressing PTPN21 resulted in elevated phosphorylation of STAT5 (Supplementary Figure S3A; HEK 293), when compared with cells that were either not treated with an agonist or transfected with the phosphatase-dead PTPN21 (PD_PTPN21). Expression of Cyclin D1 (another STAT5 target) was also evaluated, and PTPN21 expression was positively correlated with Cyclin D1 translation in both HEK 293 and SGC 7901 cells (Supplementary Figure S3B). PTPN21-dependent STAT5 activity was either absent or only slightly detectable in non-B-cell lymphoma EL4 cells (Supplementary Figure S3C). Adding to this complexity, information obtained from an open-access PrESSTo data set collected by the Fantom consortium12 described elevated levels of PTPN21 promoter binding in hematologic cells, but not B cells (Supplementary Figure S3D). It is important to note that although this study might

Letter to the Editor

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Figure 1. (A) (af) Noncancerous human gastric tissues were stained with anti-PTPN21, and then incubated with Cy3-conjugated secondary antibody or anti-E-Cadherin antibody. After staining, the samples were incubated with FITC-conjugated secondary antibody to visualize membrane-localized E-cadherin and total PTPN21 expression. (gh) Immunohistochemical staining with 3,3-diaminobenzidine (DAB; brown)

identied total PTPN21 expression, and hematoxylin (blue) was used as a nuclear counter stain. Scale bar indicates 20 m. (B) Binding activity of -casein promoter-dependent STAT5 obtained from EGF/HB-EGF treated cells was promoted when translating a rey luciferase (FLuc)

reporter containing PTPN21, but not when translating a control renilla luciferase (RLuc) reporter. The ErbB4 antagonist AG1478 impaired STAT5 binding activity. The light gray bar indicates cells transfected with empty vector and used as a control. Other bars represent cells transfected with pcDNA_PTPN21 plasmid in a dose-dependent manner (100400 ng). Cells were co-transfected with ErbB4 and/or treated with EGF/HB-EGF (50 ng/ml) or AG1478 (510 M), as indicated. (C) Constitutive STAT5A promoted -casein promoter-dependent STAT5 binding activity, whereas constitutive STAT5B failed to promote high levels of -casein promoter-dependent STAT5 binding activity. (D, E) SGC 7901 cells were co-transfected with ErbB4 and PTPN21 or phosphatase-dead mutant PD_PTPN21 for 3648 h, and then treated with EGF/HB-EGF (50 ng/ml) for 0, 5 or 30 min as indicated. Immunoblotting analysis revealed enhanced STAT5 activity after transfection with PTPN21, which manifested as increased phospho (T694)-STAT5 levels. -Casein expression levels were also analyzed. Total STAT5 protein expression and -actin housekeeping protein were used to ensure comparable total protein levels when analyzing different samples. For all tests, a signicant Po0.05 is represented with *, a Po0.01 is represented with ** and Po0.001 is represented with ***. Error bars represent the standard deviation.

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have identied a mechanistic role for PTPN21 in gastric cell lines, the lymphoma cell line stimulated with EGF showed only a slight induction of STAT5 activity, suggesting that the erythropoietin receptor remained the key transmembrane receptor for activation of STAT5 in the malignant hematopoietic cell line. Taken together, these data suggest the existence of cross talk between gastric stroma and adjacent malignant lymphoma cells, triggered by an extrinsic signaling transduction cross talk mechanism that remains to be elucidated. As a result, we further investigated the role of PTPN21 in gastric lymphoma by conducting histopathological analyses of human gastric B cells obtained from the tissue of patients with either gastric B-cell Hodgkins lymphoma (HL; n = 6) or non-Hodgkins lymphoma (NHL; n = 6).

Gastric B cells from NHL patients contained signicantly increased levels of PTPN21; however, when based on intensity and proportional scales, only moderately increased levels of PTPN21 were found in B cells from HL patients, and low levels of PTPN21 in noncancerous tissues (P-valueo0.05; MannWhitney U;

Figure 2). Lower expression of membrane E-cadherin was correlated with a higher expression of PTPN21 in human gastric B cells obtained from NHL and HL patients. In contrast, expression of cytosolic E-cadherin was positively correlated with PTPN21 expression in human gastric adenocarcinoma cells. Additional analyses of the inuence of age and gender were performed using

a tting linear model and MannWhitney U model respectively, and the results showed no correlation between PTPN21 expression and age or gender. These results suggest that elevated PTPN21 expression is both abnormal and involved in the pathogenesis of gastric B-cell NHL and HL. Overall, based on the expression proles of PTPN21 in human gastric tissues, it is clear that PTPN21 plays a less important pathologic role in adenocarcinoma than in B-cell NHL.

In addition, elevated PTPN21 levels were positively correlated with cytosolic levels of the carcinoma marker E-cadherin. Coincidentally, Pez, the Drosophila homolog of PTPN21 that colocalizes with membrane-bound E-cadherin in basolateral membranes, is known to be essential for the epithelialmesenchymal transition process.13 Overexpression of Pez has been shown to inhibit cellcell contact and abolish localization of E-cadherin to the plasma membrane.13 Such ndings support those in the present study, which showed that signicantly increased PTPN21 expression in malignant human gastric lymphoma tissue was associated with reduced E-cadherin levels on the cell membrane (Figure 2).

In summary, PTPN21 was found to be the most mutated PTP in colorectal tumors with microsatellite instability; however, its role in human malignancies remains unclear. The data presented in this report show that PTPN21 is highly expressed in human gastric

Figure 2. (A) PTPN21 is overexpressed in human gastric B-cells non-Hodgkins lymphoma tissue. (af) Malignant human gastric B-cells non-Hodgkins lymphoma. (ad) Fluorescence immunohistochemistry using anti-PTPN21 and Cy3-conjugated secondary antibody or anti-E-cadherin antibody and FITC-conjugated secondary antibody revealed membrane-localized E-cadherin and total PTPN21 expression. (ef) Immunohistochemical staining with 3,3-diaminobenzidine (DAB; brown) identied total PTPN21 expression, with hematoxylin (blue) being used as a nuclear counter stain. (B) Intensity and (C) proportion scores for PTPN21 and E-cadherin expression in noncancerous human gastric tissues (NC; n = 10), malignant non-Hodgkins (NHL; n = 6) and Hodgkins lymphoma tissue (HL; n = 6). NHL and HL samples represented byL. Scale bar indicates 20 m. For all tests, a signicant Po0.05 is represented with *, a Po0.01 is represented with ** and Po0.001 is represented with ***. Error bars represent the standard deviation.

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B-cell NHL tissue, and promotes STAT5 activity. In addition, moderate levels of PTPN21 expression were identied in samples of non-carcinoma gastric tissue. Consequently, our data suggest a role for PTPN21 in regulating STAT5 activity, and implicate PTPN21 in the tumorigenic process leading to development of hematologic-related human gastric carcinoma.

CONFLICT OF INTEREST

The authors declare no conict of interest.

ACKNOWLEDGEMENTS

The PTPN21 vector was kindly provided by Prof Antonio Feliciello, Dipartimento di Neuroscienze, Universit Federico II, Italy. The ErbB4 vector was kindly provided by Dr Paul Rammer, Danish Cancer Society Research Center, Denmark. We thank Prof Xin-Yuan Guan, Michael Su Wang and Jian Gina for their helpful suggestions and/or technical support. This work was funded by grants from Cancer Council of Western Australia (APP1057885 and APP1077920). A/Prof Evan Ingley is supported by Sock it to Sarcoma and Hollywood Private Hospital Medical Research Foundation.

JHC Plani-Lam1,2, TC Chow1, Y-H Fan1, B Garcia-Bloj2, L Cheng1,3, DY Jin1, W Hancock4,5, S Fanayan5, E Ingley2 and Y-Q Song1,3,6

1School of Biomedical Sciences (formally known as Department of Biochemistry), Li Ka Shing Faculty of Medicine, University of

Hong Kong, Hong Kong, China;

2Cancer and Cell Biology Division, Harry Perkins Institute of Medical Research and Centre for Medical Research, The University of Western

Australia, Nedlands, Western Australia, Australia;

3Laboratory of Brain and Cognitive Sciences (State Key Laboratory), University of Hong Kong, Hong Kong, China;

4Barnett Institute, Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA;

5Department of Biomedical Sciences, Macquarie University, Sydney, New South Wales, Australia and

6Centre for Genomic Sciences, University of Hong Kong, Hong Kong, China E-mail: mailto:[email protected]

Web End [email protected]

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