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10.1152/ajpgi.00419.2015

http://scihub22266oqcxt.onion/10.1152/ajpgi.00419.2015
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C4836134!4836134!26867566
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suck abstract from ncbi


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pmid26867566      Am+J+Physiol+Gastrointest+Liver+Physiol 2016 ; 310 (8): G586-98
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  • Deletion of Na+/H+ exchanger regulatory factor 2 represses colon cancer progress by suppression of Stat3 and CD24 #MMPMID26867566
  • Yoshida M; Zhao L; Grigoryan G; Shim H; He P; Yun CC
  • Am J Physiol Gastrointest Liver Physiol 2016[Apr]; 310 (8): G586-98 PMID26867566show ga
  • The Na+/H+ exchanger regulatory factor (NHERF) family of proteins is scaffolds that orchestrate interaction of receptors and cellular proteins. Previous studies have shown that NHERF1 functions as a tumor suppressor. The goal of this study is to determine whether the loss of NHERF2 alters colorectal cancer (CRC) progress. We found that NHERF2 expression is elevated in advanced-stage CRC. Knockdown of NHERF2 decreased cancer cell proliferation in vitro and in a mouse xenograft tumor model. In addition, deletion of NHERF2 in ApcMin/+ mice resulted in decreased tumor growth in ApcMin/+ mice and increased lifespan. Blocking NHERF2 interaction with a small peptide designed to bind the second PDZ domain of NHERF2 attenuated cancer cell proliferation. Although NHERF2 is known to facilitate the effects of lysophosphatidic acid receptor 2 (LPA2), transcriptome analysis of xenograft tumors revealed that NHERF2-dependent genes largely differ from LPA2-regulated genes. Activation of ?-catenin and ERK1/2 was mitigated in ApcMin/+;Nherf2?/? adenomas. Moreover, Stat3 phosphorylation and CD24 expression levels were suppressed in ApcMin/+;Nherf2?/? adenomas. Consistently, NHERF2 knockdown attenuated Stat3 activation and CD24 expression in colon cancer cells. Interestingly, CD24 was important in the maintenance of Stat3 phosphorylation, whereas NHERF2-dependent increase in CD24 expression was blocked by inhibition of Stat3, suggesting that NHERF2 regulates Stat3 phosphorylation through a positive feedback mechanism between Stat3 and CD24. In summary, this study identifies NHERF2 as a novel oncogenic protein and a potential target for cancer treatment. NHERF2 potentiates the oncogenic effects in part by regulation of Stat3 and CD24.
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