ObjectiveThe lung cancer in Xuanwei(LCXW),China,has distinctive characteristics and its morbidity and mortality are highest in China and are on the rise.The grim situation necessitates the exploration of its pathogenesis.T-UCRs transcribed from UCRs,which are genomic sequences with completely conservation among human,rat,and mouse genomes.Given UCRs extreme conservation,it has been speculated that these regions have important biological functions.Recent studies shown T-UCRs dysregulated frequently and the aberrant expression of T-UCRs played important roles in human cancers.Different cancer types have their unique T-UCR expression profiles.However,there is no research reporting about T-UCR expression profile in LCXW.Therefore,we aimed to explore T-UCR expression profile in different stages of LCXW and wish to lay a foundation for the further functional research of T-UCRs and provide new insights and ideas for the mechanism research of LCXWMethodsThe 26 paired LCXW and non-cancerous lung(NCL)tissues were divided into 3 groups according to their pathological stage.We carried out the T-UCR microarray to detect T-UCR expression profile and screen out differentially expressed T-UCRs and related genes in different staged LCXW.Then,RT-qPCR was used to validate the microarray data on 50 paired LCXW and NCL tissues.Finally,SPSS22.0 statistical software was used to analyze the association between the difference expression of candidate T-UCRs and patients' clinicopathological factors.ResultsT-UCRs and related genes significantly dysregulated in LCXW lung cancer tissues by comparison with the corresponding NCL tissues and the number of dysregulated T-UCRs and related genes present an increasing trend from I stage to III stage LCXW specimens.RT-qPCR analysis showed that uc.63-and uc.280+ were up-regulated.The relative expression levels of uc.234+and uc.208-,uc209-had no significant difference between the LCXW tissues and the NCL tissues.ConclusionOur study revealed the expression profile of T-UCRs and demonstrated that T-UCRs and related genes were aberrantly expressed in different staged LCXW.These T-UCRs and related genes may involved in the carcinogenesis of LCXW,which provides a basis for further revealing the mechanism of LCXW.Further study of these T-UCRs may provide new targets and methods for the diagnosis and therapies of LCXW. |