Senile erythroderma with low serum IgE and high titers of tumor marker, squamous cell carcinoma(SCC)-related antigens. Successful glyteer ointment therapy: Reports of 2 cases.

1989 ◽  
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Author(s):  
Kazunobu OTOYAMA ◽  
Yasuhiro HORIUCHI ◽  
Yasuhide SAITO ◽  
Tomoo YOKOTA ◽  
Mikio MASUZAWA
Cancer ◽  
2000 ◽  
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Akihiko Takeda ◽  
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Shinichi Okazumi ◽  
Hisahiro Matsubara ◽  
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1995 ◽  
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M. Barak ◽  
E. Greenberg ◽  
N. Uri ◽  
J. Kellner ◽  
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Bal Amanjit ◽  
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AbstractPURPOSECR-1 (CR-1) is an oncofetal protein with its role as a key factor in early process of carcinoma has been evaluated in cases of various cancers. However, very few studies have reported its role in oral cancers, which is the sixth most common cancer around the world, particularly with high prevalence in developing countries. Oral squamous cell carcinoma (OSCC) is the most predominant (90%) of all the histological types of oral cancer. Late detection, associated with increased morbidity and mortality, is mainly attributed to non-availability of a suitable biomarker for the disease. In the present pilot study we have evaluated the role of soluble CR-1, in serum as a potential tumor marker for OSCC.METHODSCR-1 was estimated using sandwich ELISA in serum samples of 50 biopsy proven OSCC patients (pre and post treatment) along with age and gender matched healthy controls. Immunohistochemistry was also done in corresponding tumor tissue sections to check the expression of CR-1.RESULTSPre-treatment CR-1 was found to be 2.25 fold higher in serum of OSCC patients as compared to control (p<0.0001***), which was reduced to 1.6 folds post treatment (p=0.0006***). CR-1 levels were comparatively higher in early stage of disease. Upon IHC 80% of the cases were found to be positive for CR-1.CONCLUSIONThis study provides evidence that serum levels of CR-1 are elevated in patients of Oral Squamous Cell Carcinoma, which decrease post treatment. Also, the association of expression of protein with tumor progression predicts CR-1 as a molecule that can be further evaluated as a potential tumor maker in OSCC.


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