Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Dermal non-neural granular cell tumor (NNGCT) was first described in 1991 as an S100-negative polypoid non-melanocytic tumor.
|
28266050 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Then, we found that S100B was preferentially expressed in CD133<sup>+</sup> ovarian CSLCs derived from both ovarian cancer cell lines and primary tumors of patients.
|
27501952 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Three tumors were immunoreactive for S100 protein.
|
27816723 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemical stains performed on the pleural-based mass showed tumor positivity for AE1/AE3, CK5/6, p16, and S-100.
|
28411397 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
GFAP and S100 protein expressions in tumour cells from pituitary adenomas are influenced by hormone profile.
|
28660986 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, to identify the subtype of this sarcoma, the immunohistochemical staining of the tumor was performed with each of the various antibodies and the results are epithelial membrane antigen (-), H-caldesmon (-), desmin (+), smooth muscle actin (+), S-100 (-), myogenin (-), pan-keratin (-), and Ki-67 (positive rate: 20%).
|
28248883 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Immunohistochemically, the tumour cells were variably strongly positive for expression of S100 and glial fibrillary acidic protein.
|
29169623 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemistry indicated that the tumor was positive for CK5/6 and p63, but negative for myoepithelial markers such as S-100 protein, αSMA, and calponin.
|
26297211 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemistry demonstrated tumor cell positivity for vimentin and S-100.
|
28489736 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The assessment of SPA growth in nude mice indicated an absence of tumour growth in the SPA-XT-II group (in which the XT-II gene was silenced), whereas SPA growth was observed in the other two groups (in which the XT-II gene was not silenced), and the tumour tissue was positive for the human S-100 protein, α-SMA and CK8&18.
|
27732748 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
By immunohistochemistry, these tumors show expression of S100 protein and SOX10, in the absence of expression of more specific melanocytic markers (eg, HMB45, Melan A).
|
27346570 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
S-100-expression in spindle cell lipoma may cause problems in the differential diagnosis with neural and melanocytic neoplasms and emphasizes the plasticity of the spindle cells in spindle cell lipoma.
|
27444171 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, in vivo experiments have proven the role of S100 proteins in tumour growth and disease progression, while other studies have shown their prognostic value and involvement in resistance to chemotherapy drugs.
|
25880590 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We used comprehensive histologic subtyping to provide a semiquantitive assessment of histologic patterns in each tumor and performed immunohistochemical analyses including S100/vimentin/mammaglobin/DOG1.
|
25976476 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
This Review highlights new findings regarding the role of S100 family members in cancer diagnosis and treatment, the contribution of S100 signalling to tumour biology, and the discovery and development of S100 inhibitors for treating cancer.
|
25614008 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Clear cell sarcoma-like tumor of the gastrointestinal tract is positive for S100 protein, invariably negative for melanocyte-specific markers and is often also positive for neuroendocrine markers.
|
25724038 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The percentages of tumors staining positively were as follows: micro-ophthalmia-associated transcription factor, NKI/C3, bcl-1, E-cadherin, and cathepsin K (100%); HMB-45, 4E-binding protein 1, and CD68 (88%); smooth muscle actin and muscle-specific actin (40%); S100 (38%); calponin (20%); desmin (13%); and melan-A, SOX10, and keratin (0%).
|
25267378 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Xenografts morphologically mimicked the primary tumor and expressed S-100 protein and antigens associated with melanin synthesis (Melan-A, HMB45).
|
24946937 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
S100 family of calcium-binding proteins is commonly upregulated in a variety of tumor types and is often associated with tumor progression.
|
23996929 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemistry, performed in four cases, revealed positivity for S-100 and pancytokeratin in two of three neoplasms stained for each marker.
|
23672313 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
TYRP1 mRNA expression in 104 lymph node metastases was quantified by real-time PCR and normalised to S100 calcium-binding protein B (S100B) mRNA expression to correct for tumour load.
|
23519055 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemistry showed epithelioid cells with strong nuclear and cytoplasmic staining with S-100 protein, thus establishing the diagnosis of a melanocytic tumor.
|
22985334 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Each tumour cell was positive for S100 protein and HMB-45.
|
23796270 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Neuropathological studies, assayed by immunohistochemical staining, showed that the tumor sample was positive to antibodies against S-100, CgA, AE1/AE3 (cytokeratin), Ki-67, INI1 and TP53, and was negative to antibodies against Nestin, GFAP, CD133, EMA and AFP.
|
22534715 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The third group comprised blastic plasmacytoid dendritic cell tumors (n=4), characterized by a proliferation of monomorphous medium-sized blast cells, which were CD4, CD56, CD123, TCL1 positive but CD1a and S100 negative.
|
22895265 |
2012 |