Objective: To investigate the expression and clinical significance ofCTCFL,OIP5,ACTL8and XAGE3in brain tumors and discuss thepossibility of these four CTA as target antigens for tumorimmunotherapy.Methods: The expression of CTCFL,OIP5,ACTL8and XAGE3mRNAwas detected in122cases of brain tumors using Reversetranscription-polymerase Chain Reaction (RT-PCR). The CTCFL,OIP5,ACTL8and XAGE3expression and the clinicopathologicalcharacteristics of tumors was analysed with SPSS16.0statistical software.Results: In122cases of brain tumors,the expression of four CTA wasXAGE3(49.18%,60/122),OIP5(13.93%,17/122),CTCFL(21.31%,26/122)ACTL8(24.59%,30/122), respectively; In addition, twoCTA and three CTA display the phenomenon of co-expression;Statisticalanalysis showed that there was no association between clinical data andexpression frequency of these four CTAs, except for the pathological typeand expression frequency of OIP5.Conclusion: XAGE3, OIP5, CTCFL and ACTL8expressed in braintumors,in which XAGE3have higher expression frequency,suggestingXAGE3can be as a target antigen for immunotherapy of braintumor.co-expression of several CTAs provides a new insight forimmunotherapy. |