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MicroRNA-103 Promotes Colorectal Cancer by Targeting Tumor Suppressor DICER and PTEN

机译:MicroRNA-103通过靶向肿瘤抑制因子DICER和PTEN促进结直肠癌

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MicroRNAs (miRNAs) are a class of small, noncoding RNAs that act as key regulators in various physiological and pathological processes. However, the regulatory mechanisms for miRNAs in colorectal cancer remain largely unknown. Here, we found that miR-103 is up-regulated in colorectal cancer and its overexpression is closely associated with tumor proliferation and migration. In addition, repressing the expression of miR-103 apparently inhibits colorectal cancer cell proliferation and migration in vitro and HCT-116 xenograft tumor growth in vivo. Subsequent software analysis and dual-luciferase reporter assay identified two tumor suppressor genes DICER and PTEN as direct targets of miR-103, and up-regulation of DICER and PTEN obtained similar results to that occurred in the silencing of miR-103. In addition, restoration of DICER and PTEN can inhibit miR-103-induced colorectal cancer cell proliferation and migration. Our data collectively demonstrate that miR-103 is an oncogene miRNA that promotes colorectal cancer proliferation and migration through down-regulation of the tumor suppressor genes DICER and PTEN. Thus, miR-103 may represent a new potential diagnostic and therapeutic target for colorectal cancer treatment.
机译:微小RNA(miRNA)是一类小的非编码RNA,在各种生理和病理过程中起关键调节剂的作用。但是,在大肠癌中miRNA的调控机制仍然未知。在这里,我们发现miR-103在结直肠癌中表达上调,其过表达与肿瘤的增殖和迁移密切相关。此外,抑制miR-103的表达显然会抑制结直肠癌细胞的体外增殖和迁移以及体内HCT-116异种移植肿瘤的生长。随后的软件分析和双荧光素酶报告基因分析鉴定了两个抑癌基因DICER和PTEN作为miR-103的直接靶标,DICER和PTEN的上调获得了与miR-103沉默类似的结果。另外,DICER和PTEN的恢复可以抑制miR-103诱导的结直肠癌细胞的增殖和迁移。我们的数据共同证明,miR-103是一种癌基因miRNA,可通过下调肿瘤抑制基因DICER和PTEN来促进结直肠癌的增殖和迁移。因此,miR-103可能代表了结直肠癌治疗的新潜在诊断和治疗靶标。

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