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Journal of Hematology & Oncology logoLink to Journal of Hematology & Oncology
. 2023 Feb 18;16:12. doi: 10.1186/s13045-023-01412-w

Correction : LINC01123, a c-Myc-activated long non-coding RNA, promotes proliferation and aerobic glycolysis of non-small cell lung cancer through miR-199a-5p/c-Myc axis

Qian Hua 1,#, Mingming Jin 2,#, Baoming Mi 3,#, Fei Xu 1, Tian Li 2, Li Zhao 1, Jianjun Liu 1,, Gang Huang 1,2,
PMCID: PMC9938968  PMID: 36804030

Correction : Journal of Hematology & Oncology https://doi.org/10.1186/s13045-019-0773-y

The original version of this article unfortunately contained a mistake in Fig. 7A, B. In Fig. 7A, the first, third and fourth colony was previously used by mistake with Fig. 2E. In Fig. 7B, the fourth colony was used by mistake with the fifth colony. The revised corrected Fig. 7A, , B is given below.

Fig. 7.

Fig. 7

LINC01123 functions as an oncogene via miR-199a-5p and c-Myc. a Colony formation rescue experiment showed that cell proliferation reduced by si-1123 could be increased by miR-199a-5p inhibitor or Myc-OE in H1299 cell. b Colony formation rescue experiment showed that cell proliferation stimulated by ectopic expression of LINC01123 could be repressed by miR-199a-5p mimics or si-Myc in A549 cell. ce Metabolic functional rescue experiment showed that 18F-FDG uptake, lactate production, and protein expression level of HK2 and LDHA reduced by si-1123 could be increased by miR-199a-5p inhibitor or Myc-OE in H1299 cell. fh Metabolic functional rescue experiment showed that.18F-FDG uptake, lactate production, and protein expression level of HK2 and LDHA promoted by ectopic expression of LINC01123 could be repressed by miR199a-5p mimics or si-Myc in A549 cell. Scale bar = 100 μm. Data shown are mean ± SD (n = 3) (*P < 0.05, **P < 0.01, ***P < 0.001)

Footnotes

Publisher's Note

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Qian Hua, Mingming Jin and Baoming Mi contributed equally to this work.

Contributor Information

Jianjun Liu, Email: nuclearj@163.com.

Gang Huang, Email: huanggang@sumhs.edu.cn.


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