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[B. Cell Biology/Stem Cell] B-7



                  Novel ER integral membrane protein SURF4 promotes


                          oncogenic transformation via ERK activation




                       Munju Kwon¹, Suyeon Woo¹, Jayoung Kim¹, Hee-Sun Choi¹, Dongjun Lee¹*

                    ¹Department of Convergence Medicine, Pusan National University, Yangsan 50612, Korea





        SURF4 encodes for conserved ER integral membrane protein containing multiple putative transmembrane regions.
        SURF4 is a cargo receptor that promotes protein secretion, transport, and ER export. Previous studies reported that

        SURF4 has been involved in maintaining the normal structure of the endoplasmic reticulum - Golgi compartment
        (ERGIC) and Golgi, and regulates store-operated Ca²⁺ entry (SOCE). It has also been reported to be involved in the

        replication of viruses. In one of the previous studies, the SURF4 protein was discovered through in silico analysis of
        Kaplan-Meier survival curves in pan-cancer patients. We found that by modulating the SURF4 levels, normal cells

        were  transformed  into  tumor  cells  and  it affected cell  migration  in  vitro.  SURF4 also promotes oncogenic
        transformation in vivo. Here, we further investigated the function and role of SURF4 with oncogenic potential in

        human cancer cell lines and reported that SURF4 overexpression regulates MEK or ERK activation in various solid
        cancer  cell  lines,  including  breast  cancer,  prostate  cancer,  ovarian  cancer,  and  colorectal  cancer.  These  studies

        revealed a novel molecular basis for positive regulators of MEK-ERK activation signals in solid cancer cells.
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