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Fig. 2. NAT10-silenced OS cells exhibited inhibition of proliferation, invasion, and migration. Transfection of si-NAT10#1 or si-NAT10#2 was conducted in 143B and U2OS cells, with si-NC as the control group. (A) NAT10 protein level was assayed by WB. (B) Cell viability was measured using CCK-8. (C) Proliferation ability was assessed through EdU assay. (D-F) <t>Apoptosis</t> was examined via flow cytometry (D) and <t>TUNEL</t> assay (E-F). (G) Invasive cells were determined by transwell assay. (H) Migration distance was detected via scratch assay. Error bar is mean ± SD. **P < 0.01, ***P < 0.001.
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Fig. 2. NAT10-silenced OS cells exhibited inhibition of proliferation, invasion, and migration. Transfection of si-NAT10#1 or si-NAT10#2 was conducted in 143B and U2OS cells, with si-NC as the control group. (A) NAT10 protein level was assayed by WB. (B) Cell viability was measured using CCK-8. (C) Proliferation ability was assessed through EdU assay. (D-F) Apoptosis was examined via flow cytometry (D) and TUNEL assay (E-F). (G) Invasive cells were determined by transwell assay. (H) Migration distance was detected via scratch assay. Error bar is mean ± SD. **P < 0.01, ***P < 0.001.

Journal: Journal of bone oncology

Article Title: Yin Yang 1 protein-activated N-acetyltransferase 10 drives cell malignant progression of osteosarcoma through ac4C acetylation of integrin β3

doi: 10.1016/j.jbo.2025.100701

Figure Lengend Snippet: Fig. 2. NAT10-silenced OS cells exhibited inhibition of proliferation, invasion, and migration. Transfection of si-NAT10#1 or si-NAT10#2 was conducted in 143B and U2OS cells, with si-NC as the control group. (A) NAT10 protein level was assayed by WB. (B) Cell viability was measured using CCK-8. (C) Proliferation ability was assessed through EdU assay. (D-F) Apoptosis was examined via flow cytometry (D) and TUNEL assay (E-F). (G) Invasive cells were determined by transwell assay. (H) Migration distance was detected via scratch assay. Error bar is mean ± SD. **P < 0.01, ***P < 0.001.

Article Snippet: In addition, cell apoptosis was estimated using TUNEL Apoptosis Assay Kit (Solarbio) as per the instruction book provided by the manufacturer.

Techniques: Inhibition, Migration, Transfection, Control, CCK-8 Assay, EdU Assay, Flow Cytometry, TUNEL Assay, Transwell Assay, Wound Healing Assay

Fig. 4. NAT10/ITGB3 axis contributed to OS cell malignant development. (A) Overexpression efficiency of OE-ITGB3 was evaluated using WB. (B-G) 143B and U2OS cells were transfected with si-NC, si-NAT10#1, si-NAT10#1 + OE-ITGB3. (B) CCK-8 was employed to determine cell viability. (C) EdU assay was performed to examine cell proliferation. (D-E) Flow cytometry (D) and TUNEL assay (E) were utilized for measuring cell apoptosis. (F-G) Transwell assay and scratch assay were applied for detecting invasion (F) and migration (G). Error bar is mean ± SD. **P < 0.01, ***P < 0.001.

Journal: Journal of bone oncology

Article Title: Yin Yang 1 protein-activated N-acetyltransferase 10 drives cell malignant progression of osteosarcoma through ac4C acetylation of integrin β3

doi: 10.1016/j.jbo.2025.100701

Figure Lengend Snippet: Fig. 4. NAT10/ITGB3 axis contributed to OS cell malignant development. (A) Overexpression efficiency of OE-ITGB3 was evaluated using WB. (B-G) 143B and U2OS cells were transfected with si-NC, si-NAT10#1, si-NAT10#1 + OE-ITGB3. (B) CCK-8 was employed to determine cell viability. (C) EdU assay was performed to examine cell proliferation. (D-E) Flow cytometry (D) and TUNEL assay (E) were utilized for measuring cell apoptosis. (F-G) Transwell assay and scratch assay were applied for detecting invasion (F) and migration (G). Error bar is mean ± SD. **P < 0.01, ***P < 0.001.

Article Snippet: In addition, cell apoptosis was estimated using TUNEL Apoptosis Assay Kit (Solarbio) as per the instruction book provided by the manufacturer.

Techniques: Over Expression, Transfection, CCK-8 Assay, EdU Assay, Flow Cytometry, TUNEL Assay, Transwell Assay, Wound Healing Assay, Migration

Fig. 6. Depletion of YY1 impeded OS cell growth and metastasis by down-regulating NAT10. (A) WB was implemented for NAT10 protein detection following transfection with OE-NC or OE-NAT10. (B-G) 143B and U2OS cells were divided into si-NC, si-YY1, or si-YY1 + OE-NAT10 group. (B-C) Evaluation of cell growth was administrated through CCK-8 for cell viability (B) and EdU assay for proliferation (C). (D-E) Apoptosis examination was executed via flow cytometry (D) and TUNEL assay (E). (F-G) Cell metastasis was estimated using transwell assay for invasion (F) and scratch assay for migration (G). Error bar is mean ± SD. **P < 0.01, ***P < 0.001.

Journal: Journal of bone oncology

Article Title: Yin Yang 1 protein-activated N-acetyltransferase 10 drives cell malignant progression of osteosarcoma through ac4C acetylation of integrin β3

doi: 10.1016/j.jbo.2025.100701

Figure Lengend Snippet: Fig. 6. Depletion of YY1 impeded OS cell growth and metastasis by down-regulating NAT10. (A) WB was implemented for NAT10 protein detection following transfection with OE-NC or OE-NAT10. (B-G) 143B and U2OS cells were divided into si-NC, si-YY1, or si-YY1 + OE-NAT10 group. (B-C) Evaluation of cell growth was administrated through CCK-8 for cell viability (B) and EdU assay for proliferation (C). (D-E) Apoptosis examination was executed via flow cytometry (D) and TUNEL assay (E). (F-G) Cell metastasis was estimated using transwell assay for invasion (F) and scratch assay for migration (G). Error bar is mean ± SD. **P < 0.01, ***P < 0.001.

Article Snippet: In addition, cell apoptosis was estimated using TUNEL Apoptosis Assay Kit (Solarbio) as per the instruction book provided by the manufacturer.

Techniques: Transfection, CCK-8 Assay, EdU Assay, Flow Cytometry, TUNEL Assay, Transwell Assay, Wound Healing Assay, Migration