当社グループは 3,000 以上の世界的なカンファレンスシリーズ 米国、ヨーロッパ、世界中で毎年イベントが開催されます。 1,000 のより科学的な学会からの支援を受けたアジア および 700 以上の オープン アクセスを発行ジャーナルには 50,000 人以上の著名人が掲載されており、科学者が編集委員として名高い
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700 ジャーナル と 15,000,000 人の読者 各ジャーナルは 25,000 人以上の読者を獲得
Jin X, Hong Y, Li P, Hao L and Chen M
Several studies have demonstrated the dysregulation of miR-449b-5p in numerous types of human cancers. However, the understanding of the function of miR-449b-5p the mechanisms linking its expression to the development of colorectal cancer (CRC) remains limited. The current work documented the decrease in the level of miR-449b-5p in CRC tissues as well as in CRC-derived cell lines. Functional assays indicated that the overexpression of miR-449b-5p inhibits proliferation, migration, and invasion of CRC cells. Mechanistically, the direct target of miR-449b-5p in CRC cells was identified as the catenin delta 1 (CTNND1) protein. Increased level of miR-449b-5p in CRC cells downregulated β-catenin, WNT11, cyclin D1, and MMP7. Conversely, the restoration of CTNND1 expression abrogated the inactivation of Wnt/β-catenin signaling induced by miR-449b-5p. In conclusion, the present investigation demonstrates for the first time that miR-449b-5p is capable of inhibiting the progression of CRC. This effect is achieved, at least in part, by targeting CTNND1-mediated Wnt/β-catenin signaling. The accumulated data point to miR-449b-5p as a novel target in the treatment of CRC.