[No authors listed]
BACKGROUND AND AIM:Previously study showed that the loss of the control of cAMP-dependent protein kinase A RIα RIα)/ A-kinase anchoring proteins 10 (AKAP10) signaling pathway initiate dysregulation of cellular healthy physiology leading to tumorigenesis. The aim of this study was to investigate the role of RIα/AKAP10 signaling pathway in colorectal cancer (CRC). METHODS:The AKAP10 expression at the mRNA and protein level have been analyzed in colon cancer cell lines, primary CRCs and matched normal mucosa samples, and compared in accordance with specific clinicopathological features of CRC. The correlation between expression of AKAP10 and duanyu1529 RIα were also analyzed. RESULTS:Compared with HCT116 and SW480 cells, the AKAP10 was significantly upregulated in the colon cell line KM12C and its metastatic counterparts, KM12SM and KM12L4A. Moreover, the KM12SM and KM12L4A having high metastatic potentials displayed the elevated levels of AKAP10 compared with KM12C having poor metastatic potential. A notably higher level of AKAP10 expression was found in CRC tissues at both mRNA and protein levels. Increased expression of AKAP10 in CRC patients was positively associated with the depth of invasion and the grade of differentiation. Univariate survival analysis showed that the increased expression of AKAP10 was related to poorer survival. Cox multivariate regression analysis confirmed that AKAP10 was an independent predictor of the overall survival of CRC patients. duanyu1529 RIα mRNA was also expressed at high levels in CRC. The correlation coefficient between mRNA expression of AKAP10 and duanyu1529 RIα in CRC was 0.417. AKAP10âmRNA overexpression was correlated significantly with duanyu1529 RIα. CONCLUSIONS:Our data indicated that duanyu1529 RIα/AKAP10 signaling pathway is associated with the progression and prognosis of CRC.
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