4.7 Article

miR-143-3p targeting of ITGA6 suppresses tumour growth and angiogenesis by downregulating PLGF expression via the PI3K/AKT pathway in gallbladder carcinoma

Journal

CELL DEATH & DISEASE
Volume 9, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41419-017-0258-2

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Funding

  1. National Natural Science Foundation of China [31620103910, 91440203, 81402403, 81502433, 31601021, 31501127]
  2. National High Technology Research and Development Program (863 Program) [2012AA022606]
  3. Shanghai Science and Technology Commission Key Basic Research Program [16JC1400200]
  4. Key Program of Shanghai Science and Technology Commission [16411952501]
  5. Program for Changjiang Scholars
  6. Precision Medicine Research Program of Shanghai Jiao Tong University School of Medicine [15ZH4003]
  7. Multiple Central Clinical Research Program of Shanghai Jiao Tong University School of Medicine [DLY201507]
  8. Leading Talent Program of Shanghai and Specialized Research Foundation for the PhD Program of Higher Education-Priority Development Fields [20130073130014]
  9. Interdisciplinary Program of Shanghai Jiao Tong University [14JCRY05]
  10. Shanghai Rising Stars Program [15QA1403100]

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Gallbladder cancer (GBC) is the most common malignant tumour of the biliary track system. Angiogenesis plays a pivotal role in the development and progression of malignant tumours. miR-143-3p acts as a tumour suppressor in various cancers. Their role in GBC is however less well defined. Here we show that the expression levels of miR-143-3p were decreased in human GBC tissues compared with the non-tumour adjacent tissue (NAT) counterparts and were closely associated with overall survival. We discovered that miR-143-3p was a novel inhibitor of tumour growth and angiogenesis in vivo and in vitro. Our antibody array, ELISA and PLGF rescue analyses indicated that PLGF played an essential role in the antiangiogenic effect of miR-143-3p. Furthermore, we used miRNA target-prediction software and dual-luciferase assays to confirm that integrin alpha 6 (ITGA6) acted as a direct target of miR-143-3p. Our ELISA and western blot analyses confirmed that the expression of PLGF was decreased via the ITGA6/PI3K/AKT pathway. In conclusion, miR-143-3p suppresses tumour angiogenesis and growth of GBC through the ITGA6/PI3K/AKT/PLGF pathways and may be a novel molecular therapeutic target for GBC.

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