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Altogether, these data indicate an important role for SATB1 in colorectal carcinogenesis and suggest prognostically antagonistic effects of SATB1 and SATB2. The mechanistic SATB2 is a nuclear matrix attachment region-binding transcription factor with distinct nuclear staining reaction in virtually all columnar epithelial cells and an at Nov 26, 2019 SATB2 was highly sensitive for tumours of colorectal origin and only 6.8% of the tumours completely lacked SATB2 IHC staining. the SATB2 protein in formalin-fixed, paraffin-embedded tissue stained in manual qualitative immunohistochemistry. (IHC) testing. This antibody is intended to be In their immunohistochemical study of 30 consecutive cases of invasive ductal breast adenocarcinoma, 6 cases (20%) showed weak (1+) staining for SATB2 in utility of Special AT-rich sequence binding protein-2 (SATB2) in determining the primary site. were stained for SATB2, Islet1, PAX6, TTF1, and CDX2. (1%).
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Creytens, David MD, PhD *,† Author Information * Results Positive SATB2 immunoreactivity was observed in 23 (46%) SIAs in contrast to 48 (96%) CRCs (p<0.0001). Among these, only 4 (8%) SIAs showed strong and diffuse (4+) SATB2 staining compared with 38 (76%) of CRCs (p<0.0001). Conclusions SATB2 is not entirely CRC-specific and is expressed in a subset of SIAs. Colorectal carcinoma: MMR stains Vascular invasion/serosal involvement: elastic stains (e.g. Verhoeff-van Gieson, orcein, Movat) Predict response to therapy Gastro-oesophageal and gastric carcinoma: HER2 Colorectal carcinoma: MMR stains Multiple malignancies: PD-L1 Diagnosis of dysplasia IBD-related dysplasia: SATB2, p53, b-catenin Typing of for SATB2 (0%), while only 3/27 (11%) lung carcinomas showed weak and focal SATB2 staining.
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In our study, SATB2 was positive in 2.0% of POMNs compared to in 52.8% of colonic and appendiceal tumors. 2020-09-14 · In conclusion, SATB2 stain is useful in differentiating Islet1/PAX6 positive pancreatic and rectal NETs, as the rectal NETs are typically positive for SATB2 and the pancreatic NETs are negative for SATB2. Together with other recently published studies, strong staining for SATB2 is suggestive of an appendiceal or a rectal primary.
PDF Differential expression of mucin 1 and mucin 2 in
Conclusions: SATB2 is a marker of osteoblastic differentiation in benign and malignant mesenchymal tumours.
2019-11-26 · Staining for SATB2 is useful in ovarian tumors with morphologic evidence of intestinal differentiation, or with expression of CDX2 or CK20, as most cases (98%) are typically negative . In our study, SATB2 was positive in 2.0% of POMNs compared to in 52.8% of colonic and appendiceal tumors. 2020-09-14 · In conclusion, SATB2 stain is useful in differentiating Islet1/PAX6 positive pancreatic and rectal NETs, as the rectal NETs are typically positive for SATB2 and the pancreatic NETs are negative for SATB2. Together with other recently published studies, strong staining for SATB2 is suggestive of an appendiceal or a rectal primary.
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This product, sc-81376, is recommended for immunostaining Immunofluorescence staining of U-138 MG cells using the Anti-SATB2 monoclonal antibody, showing specific staining in the nucleoplasm in green. Microtubule- First panel: typical staining pattern for an ovarian mucinous carcinoma: Hematoxylin and eosin (H&E) stain, CK7 diffuse, SATB2 absent, PAX8 nondiffuse , CDX2 mucin; PD-L1; SATB2; special stain.
Furthermore, SATB1 expression is a factor of poor prognosis in SATB2 negative tumours. Altogether, these data indicate an important role for SATB1 in colorectal carcinogenesis and suggest prognostically antagonistic effects of SATB1 and SATB2. The mechanistic
SATB2 is a nuclear matrix attachment region-binding transcription factor with distinct nuclear staining reaction in virtually all columnar epithelial cells and an at
Nov 26, 2019 SATB2 was highly sensitive for tumours of colorectal origin and only 6.8% of the tumours completely lacked SATB2 IHC staining.
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SATB2 is a supplementary immunohistochemical marker to CDX2 in the diagnosis of colorectal carcinoma metastasis in an unknown primary. Parag Deepak Dabir. Corresponding Author. E-mail address: drparagdabir@gmail.com.