Trastuzumab-treated Invasive Lobular Carcinoma patients have a differently expressed protein tyrosine phosphatase receptor type H, PTPRH

2021 ◽  
Author(s):  
Mairead Paul ◽  
Brandon Weston ◽  
Oliwier Morin

Trastuzumab, a monoclonal antibody that targets the human epidermal growth factor receptor 2 (HER2), isused to treat human breast cancer1,2. However, a thorough knowledge of how trastuzumab therapy modulatestumor signal transduction is inadequate. We discovered that the protein tyrosine phosphatase receptor type H,encoded by PTPRH, was among the genes most differentially expressed in the primary tumors of patientstreated with trastuzumab, and expressed at lower levels in the tumors of patients treated with trastuzumab, bymining published and public microarray and gene expression data3,4 from the primary tumors of patientstreated with trastuzumab. Thus, trastuzumab treatment in breast cancer patients is linked to lower primarytumor expression of a protein tyrosine phosphatase, whose deficit in pediatric solid tumors identifies a riskphenotypeand whose expression is reduced in colorectal cancer.

2021 ◽  
Author(s):  
James D. Klingensmith

Trastuzumab, a monoclonal antibody that targets the human epidermal growth factor receptor 2 (HER2), is used to treat human breast cancer1,2. However, a thorough knowledge of how trastuzumab therapy modulates tumor signal transduction is inadequate. We discovered that the protein tyrosine phosphatase receptor type H, encoded by PTPRH, was among the genes most differentially expressed in the primary tumors of patients treated with trastuzumab, and expressed at lower levels in the tumors of patients treated with trastuzumab, by mining published and public microarray and gene expression data3,4 from the primary tumors of patients treated with trastuzumab. Thus, trastuzumab treatment in breast cancer patients is linked to lower primary tumor expression of a protein tyrosine phosphatase, whose deficit in pediatric solid tumors identifies a risk-phenotype and whose expression is reduced in colorectal cancer.


2020 ◽  
Author(s):  
Shahan Mamoor

Trastuzumab, a monoclonal antibody targeted against the human epidermal growth factor receptor 2 (HER2) is utilized for the treatment of human breast cancer (1, 2), but a complete understanding of how tumor signal transduction is modulated by trastuzumab treatment is lacking. By mining published and public microarray and gene expression data (3, 4) from the primary tumors of patients treated with trastuzumab, we found that the protein tyrosine phosphatase receptor type H, encoded by PTPRH, was among the genes most differentially expressed in the primary tumors of patients treated with trastuzumab, and expressed at lower levels in the tumors of patients treated with trastuzumab. Thus, the use of trastuzumab in patients with breast cancer is associated with decreased primary tumors expression of a protein tyrosine phosphatase whose deficiency in pediatric solid tumors defines a risk-phenotype (5) and whose expression is decreased in colorectal cancer (6).


2021 ◽  
Author(s):  
Shahan Mamoor

Epithelial ovarian cancer (EOC) is the most lethal gynecologic cancer (1). We performed discovery of genes associated with epithelial ovarian cancer and of the high-grade serous ovarian cancer (HGSC) subtype, using published microarray data (2, 3) to compare global gene expression profiles of normal ovary or fallopian tube with that of primary tumors from women diagnosed with epithelial ovarian cancer or HGSC. We identified the gene encoding protein tyrosine phosphatase, non-receptor type 6, PTPN6, as among the genes whose expression was most different in epithelial ovarian cancer as compared to the normal fallopian tube. PTPN6 expression was significantly higher in high-grade serous ovarian tumors relative to normal fallopian tube. PTPN6 expression correlated with progression-free survival in patients with ovarian cancer. These data indicate that expression of PTPN6 is perturbed in epithelial ovarian cancers broadly and in ovarian cancers of the HGSC subtype. PTPN6 may be relevant to pathways underlying ovarian cancer initiation (transformation) or progression.


2021 ◽  
pp. jclinpath-2020-206927
Author(s):  
Maryam Ahmed Al Barashdi ◽  
Ahlam Ali ◽  
Mary Frances McMullin ◽  
Ken Mills

The leucocyte common antigen, protein tyrosine phosphatase receptor type C (PTPRC), also known as CD45, is a transmembrane glycoprotein, expressed on almost all haematopoietic cells except for mature erythrocytes, and is an essential regulator of T and B cell antigen receptor-mediated activation. Disruption of the equilibrium between protein tyrosine kinase and phosphatase activity (from CD45 and others) can result in immunodeficiency, autoimmunity, or malignancy. CD45 is normally present on the cell surface, therefore it works upstream of a large signalling network which differs between cell types, and thus the effects of CD45 on these cells are also different. However, it is becoming clear that CD45 plays an essential role in the innate immune system and this is likely to be a key area for future research. In this review of PTPRC (CD45), its structure and biological activities as well as abnormal expression of CD45 in leukaemia and lymphoma will be discussed.


2021 ◽  
Vol 26 ◽  
pp. 100974
Author(s):  
Shaoting Zhang ◽  
Liangying Zhang ◽  
Zongying Jiang ◽  
Yue Guo ◽  
Hui Zhao ◽  
...  

1993 ◽  
Vol 268 (14) ◽  
pp. 10573-10581
Author(s):  
J.B. Levy ◽  
P.D. Canoll ◽  
O. Silvennoinen ◽  
G. Barnea ◽  
B. Morse ◽  
...  

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