4.8 Article

Targeting YAP1/LINC00152/FSCN1 Signaling Axis Prevents the Progression of Colorectal Cancer

Journal

ADVANCED SCIENCE
Volume 7, Issue 3, Pages -

Publisher

WILEY
DOI: 10.1002/advs.201901380

Keywords

colorectal cancer; FSCN1; Hippo pathway; LINC00152; YAP1

Funding

  1. National Natural Science Foundation of China [81874170, 81560385, 81672889, 81972663, 81903032]
  2. China 111 Project [111-2-12]
  3. Postgraduate Research and Innovation Project of Hunan Province [CX2018B115]
  4. Youth Fund of Xiangya Hospital [2018Q011]
  5. China Postdoctoral Science Foundation [2017M610462]
  6. Hunan Province Science and Technology Project [2016JC2035]
  7. Student Innovation Project of Central South University [2018zzts044]
  8. Strategic Priority Research Program of Central South University [ZLXD2017004]
  9. Graduate Research and Innovation Projects of Hunan Province [CX20190144]

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As a transcription coactivator, Yes-associated protein 1 (YAP1)'s role in tumorigenesis is well established. However, the mechanism of YAP1-regulating long noncoding RNAs (lncRNA) in tumors is still largely unknown. Here, a YAP1 target gene, long intergenic noncoding RNA 00152 (LINC00152), which is highly expressed in colorectal cancer (CRC), is identified. The oncogenic functions of LINC00152 in CRC are demonstrated by a panel of in vitro and in vivo experiments. Further studies reveal the potential downstream mechanisms of LINC00152, which can act as a competing endogenous RNA sponging with miR-632 and miR-185-3p to regulate Fascin actin-bundling protein 1 (FSCN1) expression and thus promote the malignant proliferation and metastasis in CRC cells. Targeting the YAP1/LINC00152/FSCN1 axis inhibits the progression of CRC. This finding provides a new regulatory model of the YAP1-lncRNA in CRC, which gives rise to a new perspective, YAP1/LINC00152/miR-632-miR-185-3p/FSCN1, to explore the cancer-promoting mechanism of YAP1 involved in CRC.

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