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Volume 2, Issue 8, Pages (August 2015)

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1 Volume 2, Issue 8, Pages 851-858 (August 2015)
Associations between proteasomal activator PA28γ and outcome of oral squamous cell carcinoma: Evidence from cohort studies and functional analyses  Jing Li, Xiaodong Feng, Chongkun Sun, Xin Zeng, Liang Xie, Hao Xu, Taiwen Li, Ruinan Wang, Xiaoping Xu, Xikun Zhou, Min Zhou, Yu Zhou, Hongxia Dan, Zhiyong Wang, Ning Ji, Peng Deng, Ga Liao, Ning Geng, Yun Wang, Dunfang Zhang, Yunfeng Lin, Ling Ye, Xinhua Liang, Longjiang Li, Gang Luo, Lu Jiang, Zhi Wang, Qianming Chen  EBioMedicine  Volume 2, Issue 8, Pages (August 2015) DOI: /j.ebiom Copyright © 2015 The Authors Terms and Conditions

2 Fig. 1 Study flow chart. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

3 Fig. 2 Overall Survival (OS) of OSCC patients with high and low expression of PA28γ in Three cohorts defined by the Kaplan–Meier survival curves. (a) Overall Survival in CD-I cohort. (b) Overall Survival in CD-II cohort. (c) Overall Survival in CD-I and -II cohorts. (d) Overall Survival in GZ cohort. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

4 Fig. 3 ROC curves for all-cause death of OSCC patients with or without PA28γ expression in three cohorts of two independent centers. (a) ROC curve for Model 3 in CD-I and -II Cohorts. (b) ROC curve for Model 3 in GZ cohort. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

5 Fig. 4 Functional role of PA28γ on the tumor growth. (a) Colony formation assay. PA28γ silencing led to colony formation inhibition in two OSCC cell lines (HSC-3 and CAL-27), after 10days transfection with siRNA. All data are presented as the mean±SD of three independent experiments (*P<0.05). (b) PA28γ silencing induced the apoptosis in OSCC cells, determined by Flow Cytometry assay, after 48h transfection with siRNA. All data are presented as the mean±SD of three independent experiments (*P<0.05). (c) Chemically-modified PA28γ-si could inhibit PA28γ gene expression in HSC-3, illustrated by qPCR, 48h. All data are presented as the mean±SD of three independent experiments (*P<0.05) (d ande) The tumor volumes (mean±SD) of PA28γ-si group were significantly smaller compared to the other two groups, 30days after injecting transfected cells. (n=5, *P<0.05). EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

6 Fig. S1 PA28γ staining pattern in both normal and tumor tissues. The staining of PA28γ in two selected tumor but not normal tissues has very clear nuclear positive, as shown by IHC assay. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

7 Fig. S2 Expression of PA28γ related to carcinogenesis and prognosis in OSCC cells and human tissues. (a) Validation of PA28γ over-expression in six OSCC cells compared with normal oral keratinocyte by Western blot as described in material and methods. (b) Validation the role of PA28γ expression in OSCC prognosis in 118 clinical OSCC samples. IHC staining showed those cases with poorer prognosis exhibited stronger staining. Left: a moderate-differentiated OSCC sample with disease free survival. Middle: a well-differentiated OSCC sample with regional neck recurrence within 2years postoperation. Right: a well-differentiated OSCC sample with cancer-related death with 4year's postoperation. The scale bar represents 100μm. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

8 Fig. S3 TCGA database analysis of HNSCC patients with high and low expression of PA28γ. (a) TCGA database analysis of PA28γ mRNA abundance in human primary oral cancers compared with human normal oral tissue. (b). Kaplan–Meier plot of estimated 5-year Overall Survival time distributions according to PA28γ mRNA expression. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

9 Fig. S4 Disease-Free Survival (DFS) of OSCC patients with high and low expression of PA28γ in Three cohorts defined by the Kaplan–Meier survival curves. (a) DFS in CD-I cohort. (b) DFS in CD-II cohort. (c) DFS in CD-I and -II cohorts. (d) DFS in GZ Cohort. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

10 Fig. S5 ROC curves for all-cause death of OSCC patients with or without PA28γ expression in three cohorts of two independent centers. (a) ROC curve for Model 4 in CD-I and -II cohorts. (b) ROC curve for Model 4 in GZ cohort. EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

11 Fig. S6 PA28γ silencing induced growth inhibition of OSCC cells. (a) siRNA-003 worked the best among the three strains of siRNA against PA28γ gene expression, illustrated by qPCR, 48h. (b) MTT assay, 48h. PA28γ silencing inhibited the survival of OSCC cells (HSC-3, CAL-27) but not in immortalized oral keratinocytes (HOK). The percentages of surviving cells for each of two OSCC cell lines relative to controls (defined as 100% survival). All data are represented as the mean±SD from three independent experiments (*P<0.05). EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

12 Fig. S7 PA28γ silencing induced apoptosis of OSCC cells. (a) PA28γ silencing induced the apoptosis in OSCC (HSC-3, CAL-27) cells, illustrated by propidium iodide (PI) assay, 48h. Cells undergoing apoptosis and nuclear fragmentation are indicated by arrows. The scale bar represents 50μm. All data are represented as the mean±SD from three independent experiments (*P<0.05). (b) PA28γ silencing induced the apoptosis in OSCC (HSC-3, CAL-27) cells, as shown by TUNEL assay, 36h. For each coverslip, ≧500 cells were counted. The scale bar represents 50μm. All data are represented as the mean±SD from three independent experiments (*P<0.05). EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

13 Fig. S8 PA28γ silencing decreased the migration and invasion of OSCC cells. (a) Cell migration was decreased by silencing PA28γ in OSCC cell lines (CAL-27, HSC-3), as shown by transwell migration assay, 24h. Cells that migrated to the bottom of the chamber were counted in five fields under 20× magnification. The scale bar represents 50μm. Error bars mean±SD (*P<0.05). (b) Cell invasion was decreased by silencing PA28γ in OSCC cell lines, as shown by invasion assay, 30h (right panels, scale bars represent 50μm). Cells that invaded to the bottom of the chamber were counted in five fields under 20× magnification. Error bars mean±SD (*P<0.05). EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

14 Fig. S9 Functional role of PA28γ on tumor growth. PA28γ-si could inhibit PA28γ expression in an OSCC xenografts model; angiogenesis in tumors was detected by CD34 staining. The average number of microvessels per vascular hot spot (mean±SD) was significantly lower in PA28γ-si group tissues compared with those in the two control groups; Percentages of PCNA-positive nuclei (mean±SD) in PA28γ-si group were significantly lower than those in the two control groups; Apoptosis was assessed by TUNEL assay. The scale bar represents 100μm. (*P<0.05). EBioMedicine 2015 2, DOI: ( /j.ebiom ) Copyright © 2015 The Authors Terms and Conditions

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