Open Access Article
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Correction: MicroRNA-mediated silence of onco-lncRNA MALAT1 in different ESCC cells via ligand-functionalized hydroxyl-rich nanovectors
Rui-Quan Lia,
Yanli Rena,
Wenjuan Liub,
Wenting Pana,
Fu-Jian Xu*a and
Ming Yang*b
aState Key Laboratory of Chemical Resource Engineering, Key Laboratory of Carbon Fiber and Functional Polymers (Ministry of Education), Beijing Laboratory of Biomedical Materials, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China. E-mail: xufj@mail.buct.edu.cn
bShandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital affiliated to Shandong University, Shandong Academy of Medical Sciences, Jinan, Shandong Province 250117, China. E-mail: aaryoung@yeah.net
First published on 15th May 2026
Abstract
Correction for ‘MicroRNA-mediated silence of onco-lncRNA MALAT1 in different ESCC cells via ligand-functionalized hydroxyl-rich nanovectors’ by Rui-Quan Li et al., Nanoscale, 2017, 9, 2521–2530.
The authors regret that an incorrect siR-M group Transwell assay image was accidently featured in Fig. 7Bb1 in the original article. The authors now provide the correct siR-M group Transwell assay image (below) and confirm that this change does not affect the results and conclusions presented.
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| Fig. 1 s-PGEA-FA/miR-101, s-PGEA-FA/miR-217, and s-PGEA-FA/siR-M complexes inhibit the ability of invasion of ESCC cells. Matrigel transwell assays in (A) KYSE30 and (B) KYSE450 cells: (a1 and b1) representative images of cells at the lower wells of chambers after 48 h transfection and (a2 and b2) numbers of cells which were harvested on the surface of lower wells. Error bars represent the standard deviation of three measurements (*P < 0.05). | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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