This article has been corrected: The authors have identified the errors in the affiliations listed for Tian Xie. In the affiliation 2 the "Department of Neurosurgery of Affiliated Hospital" was removed:

2Key Laboratory of Elemene Anti-Cancer Medicine of Zhejiang Province and Holistic Integrative Pharmacy Institutes, Hangzhou Normal University, Hangzhou 311121, China

The affiliation 3 was also present and has now been removed.

Xingxing Xu1,2,3,*, Xiya Shen1,2,3,*, Wenjin Feng4,*, Danlu Yang1,2,3, Lingting Jin1,2,3, Jiaojiao Wang1,2,3, Mianxian Wang1,2,3, Zhang Ting6, Feng Xue1, Jingjing Zhang1,2,3, Chaobo Meng1, Roumeng Chen1, Xinru Zheng1, Leilei Du1, Lina Xuan1, Ying Wang5, Tian Xie2, Zhihui Huang1,2,3

1School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou 325035, Zhejiang, China

2Key Laboratory of Elemene Anti-Cancer Medicine of Zhejiang Province and Holistic Integrative Pharmacy Institutes, Hangzhou Normal University, Hangzhou 311121, China

3Department of Orthopedics (Spine Surgery), The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, Zhejiang, China

4Zhejiang Sinogen Medical Equipment Co., Ltd., Wenzhou 325000, Zhejiang, China

5Department of Transfusion Medicine, Zhejiang Provincial People’s Hospital of Hangzhou Medical College, Hangzhou 310053, China

6Department of Neurobiology, Key Laboratory of Medical Neurobiology, Ministry of Health of China, School of Medicine, Zhejiang University, Hangzhou 310058, China

*Equal contribution

Additionally, the authors have identified an inadvertent error in the organization of Figure 7F. Due to the high similarity between the Western Blot raw data bands for CDK6 and Lamin B1, the Lamin B1 band in Figure 7F was mistakenly represented using the same raw band as CDK6. The authors have replaced the incorrect image with the correct original image for Lamin B1. They have also stated that this correction does not affect the experimental outcome or the conclusions of the study and sincerely apologize for this error and any inconvenience it may have caused.

The corrected version of Figure 7 is provided below.

Overexpression of YAP restored D-gal-induced GBM senescence. (A) A schematic illustration showing YAP transfection in C6 senescent cells. (B) Immunostaining of PH3 in control C6 cells without transfection, or senescent C6 cells (treated with 222 mM D-gal for 8 d) transfected with EGFP or YAP-EGFP plasmid (YAP-Res) for 2 d. (C) Quantitative analysis of the percentage of PH3+ cells over total C6 cells as shown in (B) (n = 15). (D) Representative images showing β-galactosidase staining in control C6 cells without transfection, or senescent C6 cells (treated with 222 mM D-gal for 8 d) transfected with EGFP or YAP-EGFP plasmid (YAP-Res) for 2 d. (E) Quantification of the percentage of β-galactosidase+ cells over total cells as shown in (D) (n = 15). (F) Western blot detected the expression of YAP, CDK6, and Lamin B1 in control C6 cells without transfection, or senescent C6 cells (treated with 222 mM D-gal for 8 d) transfected with EGFP or YAP-EGFP plasmid (YAP-Res) for 2 d. (G, H) Quantification of CDK6 and Lamin B1 level as shown in (F) (n = 10). Scale bars, 20 μm. Data shown are mean ± s.e.m. *P **P ***P

Figure 7. Overexpression of YAP restored D-gal-induced GBM senescence. (A) A schematic illustration showing YAP transfection in C6 senescent cells. (B) Immunostaining of PH3 in control C6 cells without transfection, or senescent C6 cells (treated with 222 mM D-gal for 8 d) transfected with EGFP or YAP-EGFP plasmid (YAP-Res) for 2 d. (C) Quantitative analysis of the percentage of PH3+ cells over total C6 cells as shown in (B) (n = 15). (D) Representative images showing β-galactosidase staining in control C6 cells without transfection, or senescent C6 cells (treated with 222 mM D-gal for 8 d) transfected with EGFP or YAP-EGFP plasmid (YAP-Res) for 2 d. (E) Quantification of the percentage of β-galactosidase+ cells over total cells as shown in (D) (n = 15). (F) Western blot detected the expression of YAP, CDK6, and Lamin B1 in control C6 cells without transfection, or senescent C6 cells (treated with 222 mM D-gal for 8 d) transfected with EGFP or YAP-EGFP plasmid (YAP-Res) for 2 d. (G, H) Quantification of CDK6 and Lamin B1 level as shown in (F) (n = 10). Scale bars, 20 μm. Data shown are mean ± s.e.m. *P < 0.05, **P < 0.01. ***P < 0.001.