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Tumor Discovery                                                      RAGEs in oral squamous cell carcinoma








                                   Limitations  Not mentioned   Tumor thickness   cannot be determined   on biopsy derived   material  No correlations   between RAGE   and histological   differentiation








                                   Inference  RAGE-H suggests   low disease-free   survival rate.  The RAGE   expression   decreases in OSCC   as they become less   differentiated  RAGE plays a   function in the   expression of VEGF   in tumors, which   is linked to tumor   angiogenesis




                                   P-value  P < 0.00001  P < 0.05       P = 0.0123   and 0.0344,   respectively








                                   Observation  The disease-free survival   rate of RAGE-H patients   was considerably lower   than that of individuals   with a low grade.  10 of 10 (100%) well-  differentiated OSCCs were   RAGE-positive, while   0 of 8 (0%) were poorly   differentiated.  Reduced band intensity at   the molecular weight 55   kDa, seen more in OSCC   than normal control.  HSC-3 and HSC-4 cells   treated with RAGE   antisense S-ODN secreted   considerably l










                                   Method  IHC      IHC        Western Blot  Elisa   RAGE: Receptors of advanced glycation end products, VEGF: Vascular endothelial growth factor, AGE: Advanced glycation end products, IHC: Immunohistochemistry, PCR: Polymerase chain





                                   Marker  RAGE     RAGE                RAGE  VEGF



                                   Control  _       14                  20




                                   Case   74        38                  20



                                   Cell   line  _   _

                               Table 1. (Continued)  Number   Study  of   samples  74  Sasahira    et al. [16]  50  Landesberg   et al. [22]  40  Sasahira    et al. [23]  reaction











            Volume 2 Issue 1 (2023)                         4                           https://doi.org/10.36922/td.244
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