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Cell Mol Neurobiol
Cell Mol Neurobiol
Cellular and Molecular Neurobiology
0272-4340
1573-6830
Springer US New York

39292316
1495
10.1007/s10571-024-01495-0
Correction
Correction: Upregulation of miR-107 Inhibits Glioma Angiogenesis and VEGF Expression
Chen Lei 12
Li Zong-yang 2
Xu Sui-yi 2
Zhang Xie-jun 2
Zhang Yuan 2
Luo Kun 3
Li Wei-ping liweiping60@139.com

12
1 https://ror.org/0064kty71 grid.12981.33 0000 0001 2360 039X Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China
2 grid.263488.3 0000 0001 0472 9649 Department of Neurosurgery, Shenzhen Key Laboratory of Neurosurgery, Shenzhen Second People’s Hospital, Shenzhen University 1st Affiliated Hospital, 3002# Sungang Road, Shenzhen, 518035 China
3 https://ror.org/0207yh398 grid.27255.37 0000 0004 1761 1174 School of Medicine, Shandong University, Jinan, China
18 9 2024
18 9 2024
12 2024
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2024
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pmcCorrection to: Cell Mol Neurobiol (2016) 36:113–120 10.1007/s10571-015-0225-3

The original version of this article unfortunately contained errors in figures.

In Fig. 2C, the migration image on the right side of the 0-h group in the scratch assay of A172 cells was incorrect and in Fig. 3A, the fluorescent images of the U87 cell group were incorrectly arranged, leading to inaccuracies in the images.

The corrected Figs. 2 and 3 are presented here.Fig. 2 Overexpression of miR-107 in glioma cells inhibits HBMVEC proliferation and migration in vitro. a U87 and A172 cells (green fluorescence, transduced with GFP or miR-107) were co-cultured with HBMVECs (red fluorescence, stained with PKH26) in six-well plates. Representative images, obtained 24 h later, are shown (9200 magnification). Scale bars 100 lm. b The effect of supernatant derived from U87 and A172 cells transduced with GFP or miR-107 on HBMVECs proliferation. Representative images are shown. Scale bars 100 lm. c Representative fluorescence microscopy image (9100 magnification) showing the effects of the supernatant fractions of U87 and A172 cells (transduced with GFP or miR-107) on HBMVEC (red fluorescence, stained with PKH26) migration in the wound-healing assay. Images were acquired directly after scratching (t = 0) and 24 h later (t = 24). Scale bars 200 lm. d The numbers of HBMVECs cocultured with U87 and A172 glioma cells (transduced with GFP or miR-107) were calculated using ImageJ software. e Quantitation of the number of HBMVECs after treated with supernatant derived from U87 and A172 cells transduced with GFP or miR-107 using ImageJ software. f Quantitation of HBMVEC migration to the scratch using ImageJ software. *P < 0.05. GFP transduced with GFP only, miR-107 transduced with GFP and miR-107

Fig. 3 Upregulation of miR-107 in glioma cells suppresses tubule formation in the HBMVEC and glioma cell co-culture system. a, b U87 or A172 glioma cells (green fluorescence, transduced with GFP or miR-107) and HBMVECs (red fluorescence, stained with PKH26) were co-cultured on Matrigel-coated plates, and tubule formation assessed after 48 h. Representative images are shown (9100). Scale bars 150 lm. c ImageJ software was applied to evaluate tubule crosses in a, b. *P < 0.05. GFP transduced with GFP only, miR-107 transduced with GFP and miR-107

The original article has been corrected.

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Lei Chen and Zong-yang Li have contributed equally to this work.
