4.7 Article

Circular RNA F-circSR derived from SLC34A2-ROS1 fusion gene promotes cell migration in non-small cell lung cancer

期刊

MOLECULAR CANCER
卷 18, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12943-019-1028-9

关键词

SLC34A2-ROS1; Circular RNA; Cell migration; NSCLC

资金

  1. National Key RAMP
  2. D Program of China [2017YFA0504304, 2016YFA0502204]
  3. National Natural Science Foundation of China [81772960, 81572739]
  4. Sichuan Science AMP
  5. Technology Program [2019JDTD0013]
  6. 1.3.5 Project for Disciplines of Excellence, West China Hospital, Sichuan University [ZYJC18030]
  7. China Postdoctoral Science Foundation [0040234153024]
  8. Postdoctoral Foundation of Sichuan University [20826041C4144]

向作者/读者索取更多资源

Cancer-associated chromosomal translocations are reported to generate oncogenic circular RNA (circRNA), contributing to tumorigenesis. The fusion gene SLC34A2-ROS1 (solute carrier family 34 member 2 and ROS proto-oncogene 1) plays an important role in non-small cell lung cancer (NSCLC) progression. However, whether SLC34A2-ROS1 gene can produce circRNA remains unknown. Here, we identified two novel circRNAs (F-circSR1 and F-circSR2) generated from SLC34A2-ROS1 fusion gene, while F-circSR1 has higher expression than F-circSR2. Functional studies through gain- and loss-of-function strategies showed that both F-circSRs promote cell migration in lung cancer cells, whereas they have little effect on cell proliferation. Using the minigene GFP reporter assay, we verified that the flanking complementary sequences with canonical splicing sites are essential for F-circSR biogenesis. Therefore, our findings demonstrate the oncogenic role of F-circSR in NSCLC and highlight its therapeutic potential.

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