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Knockdown of LINC00092 in the KYSE170 cell line. (A) Validation of LINC00092 expression in the knockdown cell line (n=3). KYSE170 cells were transfected with a si-NC or a si-LINC00092, with untransfected cells as an additional control. The relative mRNA expression level of LINC00092 was quantified by <t>qRT-PCR.</t> Data were analyzed by one-way ANOVA. (B) Cell viability assessed by MTT assay in control, si-NC, and si-LINC00092 groups at 0, 24, 48, and 72 hours post-transfection (n=3). Data were analyzed by two-way ANOVA. (C) Results of the colony formation assay in LINC00092 knockdown cells (n=3) (crystal violet staining). Data were analyzed by one-way ANOVA. (D) Results of the wound healing scratch assay in LINC00092 knockdown cells (n=3) (×100). Data were analyzed by one-way ANOVA. (E) Results of invasion assays in LINC00092 knockdown cells (n=3) (crystal violet staining, ×200). Data were analyzed by one-way ANOVA. (F) Results of flow cytometry analysis of apoptosis in LINC00092 knockdown cells (n=3). Data were analyzed by one-way ANOVA. **, P<0.01; ***, P<0.001. ANOVA, analysis of variance; FITC, fluorescein isothiocyanate; LINC00092, long intergenic non-protein-coding RNA 92; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; OD, optical density; PI, propidium iodide; si-LINC00092, LINC00092-targeting siRNA; si-NC, non-targeting siRNA negative control; siRNA, small interfering RNA; qRT-PCR, quantitative real-time polymerase chain reaction.
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Knockdown of LINC00092 in the KYSE170 cell line. (A) Validation of LINC00092 expression in the knockdown cell line (n=3). KYSE170 cells were transfected with a si-NC or a si-LINC00092, with untransfected cells as an additional control. The relative mRNA expression level of LINC00092 was quantified by <t>qRT-PCR.</t> Data were analyzed by one-way ANOVA. (B) Cell viability assessed by MTT assay in control, si-NC, and si-LINC00092 groups at 0, 24, 48, and 72 hours post-transfection (n=3). Data were analyzed by two-way ANOVA. (C) Results of the colony formation assay in LINC00092 knockdown cells (n=3) (crystal violet staining). Data were analyzed by one-way ANOVA. (D) Results of the wound healing scratch assay in LINC00092 knockdown cells (n=3) (×100). Data were analyzed by one-way ANOVA. (E) Results of invasion assays in LINC00092 knockdown cells (n=3) (crystal violet staining, ×200). Data were analyzed by one-way ANOVA. (F) Results of flow cytometry analysis of apoptosis in LINC00092 knockdown cells (n=3). Data were analyzed by one-way ANOVA. **, P<0.01; ***, P<0.001. ANOVA, analysis of variance; FITC, fluorescein isothiocyanate; LINC00092, long intergenic non-protein-coding RNA 92; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; OD, optical density; PI, propidium iodide; si-LINC00092, LINC00092-targeting siRNA; si-NC, non-targeting siRNA negative control; siRNA, small interfering RNA; qRT-PCR, quantitative real-time polymerase chain reaction.
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Knockdown of LINC00092 in the KYSE170 cell line. (A) Validation of LINC00092 expression in the knockdown cell line (n=3). KYSE170 cells were transfected with a si-NC or a si-LINC00092, with untransfected cells as an additional control. The relative mRNA expression level of LINC00092 was quantified by <t>qRT-PCR.</t> Data were analyzed by one-way ANOVA. (B) Cell viability assessed by MTT assay in control, si-NC, and si-LINC00092 groups at 0, 24, 48, and 72 hours post-transfection (n=3). Data were analyzed by two-way ANOVA. (C) Results of the colony formation assay in LINC00092 knockdown cells (n=3) (crystal violet staining). Data were analyzed by one-way ANOVA. (D) Results of the wound healing scratch assay in LINC00092 knockdown cells (n=3) (×100). Data were analyzed by one-way ANOVA. (E) Results of invasion assays in LINC00092 knockdown cells (n=3) (crystal violet staining, ×200). Data were analyzed by one-way ANOVA. (F) Results of flow cytometry analysis of apoptosis in LINC00092 knockdown cells (n=3). Data were analyzed by one-way ANOVA. **, P<0.01; ***, P<0.001. ANOVA, analysis of variance; FITC, fluorescein isothiocyanate; LINC00092, long intergenic non-protein-coding RNA 92; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; OD, optical density; PI, propidium iodide; si-LINC00092, LINC00092-targeting siRNA; si-NC, non-targeting siRNA negative control; siRNA, small interfering RNA; qRT-PCR, quantitative real-time polymerase chain reaction.
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Knockdown of LINC00092 in the KYSE170 cell line. (A) Validation of LINC00092 expression in the knockdown cell line (n=3). KYSE170 cells were transfected with a si-NC or a si-LINC00092, with untransfected cells as an additional control. The relative mRNA expression level of LINC00092 was quantified by <t>qRT-PCR.</t> Data were analyzed by one-way ANOVA. (B) Cell viability assessed by MTT assay in control, si-NC, and si-LINC00092 groups at 0, 24, 48, and 72 hours post-transfection (n=3). Data were analyzed by two-way ANOVA. (C) Results of the colony formation assay in LINC00092 knockdown cells (n=3) (crystal violet staining). Data were analyzed by one-way ANOVA. (D) Results of the wound healing scratch assay in LINC00092 knockdown cells (n=3) (×100). Data were analyzed by one-way ANOVA. (E) Results of invasion assays in LINC00092 knockdown cells (n=3) (crystal violet staining, ×200). Data were analyzed by one-way ANOVA. (F) Results of flow cytometry analysis of apoptosis in LINC00092 knockdown cells (n=3). Data were analyzed by one-way ANOVA. **, P<0.01; ***, P<0.001. ANOVA, analysis of variance; FITC, fluorescein isothiocyanate; LINC00092, long intergenic non-protein-coding RNA 92; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; OD, optical density; PI, propidium iodide; si-LINC00092, LINC00092-targeting siRNA; si-NC, non-targeting siRNA negative control; siRNA, small interfering RNA; qRT-PCR, quantitative real-time polymerase chain reaction.
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Knockdown of LINC00092 in the KYSE170 cell line. (A) Validation of LINC00092 expression in the knockdown cell line (n=3). KYSE170 cells were transfected with a si-NC or a si-LINC00092, with untransfected cells as an additional control. The relative mRNA expression level of LINC00092 was quantified by qRT-PCR. Data were analyzed by one-way ANOVA. (B) Cell viability assessed by MTT assay in control, si-NC, and si-LINC00092 groups at 0, 24, 48, and 72 hours post-transfection (n=3). Data were analyzed by two-way ANOVA. (C) Results of the colony formation assay in LINC00092 knockdown cells (n=3) (crystal violet staining). Data were analyzed by one-way ANOVA. (D) Results of the wound healing scratch assay in LINC00092 knockdown cells (n=3) (×100). Data were analyzed by one-way ANOVA. (E) Results of invasion assays in LINC00092 knockdown cells (n=3) (crystal violet staining, ×200). Data were analyzed by one-way ANOVA. (F) Results of flow cytometry analysis of apoptosis in LINC00092 knockdown cells (n=3). Data were analyzed by one-way ANOVA. **, P<0.01; ***, P<0.001. ANOVA, analysis of variance; FITC, fluorescein isothiocyanate; LINC00092, long intergenic non-protein-coding RNA 92; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; OD, optical density; PI, propidium iodide; si-LINC00092, LINC00092-targeting siRNA; si-NC, non-targeting siRNA negative control; siRNA, small interfering RNA; qRT-PCR, quantitative real-time polymerase chain reaction.

Journal: Journal of Thoracic Disease

Article Title: Long non-coding RNA LINC00092 inhibits esophageal squamous cell carcinoma progression by promoting ferroptosis through the MAZ/NFE2L2 axis

doi: 10.21037/jtd-2025-1-2433

Figure Lengend Snippet: Knockdown of LINC00092 in the KYSE170 cell line. (A) Validation of LINC00092 expression in the knockdown cell line (n=3). KYSE170 cells were transfected with a si-NC or a si-LINC00092, with untransfected cells as an additional control. The relative mRNA expression level of LINC00092 was quantified by qRT-PCR. Data were analyzed by one-way ANOVA. (B) Cell viability assessed by MTT assay in control, si-NC, and si-LINC00092 groups at 0, 24, 48, and 72 hours post-transfection (n=3). Data were analyzed by two-way ANOVA. (C) Results of the colony formation assay in LINC00092 knockdown cells (n=3) (crystal violet staining). Data were analyzed by one-way ANOVA. (D) Results of the wound healing scratch assay in LINC00092 knockdown cells (n=3) (×100). Data were analyzed by one-way ANOVA. (E) Results of invasion assays in LINC00092 knockdown cells (n=3) (crystal violet staining, ×200). Data were analyzed by one-way ANOVA. (F) Results of flow cytometry analysis of apoptosis in LINC00092 knockdown cells (n=3). Data were analyzed by one-way ANOVA. **, P<0.01; ***, P<0.001. ANOVA, analysis of variance; FITC, fluorescein isothiocyanate; LINC00092, long intergenic non-protein-coding RNA 92; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; OD, optical density; PI, propidium iodide; si-LINC00092, LINC00092-targeting siRNA; si-NC, non-targeting siRNA negative control; siRNA, small interfering RNA; qRT-PCR, quantitative real-time polymerase chain reaction.

Article Snippet: PCR reaction mixtures were prepared using the Luna ® universal One-Step qRT-PCR Kit (SYBR; New England Biolabs).

Techniques: Knockdown, Biomarker Discovery, Expressing, Transfection, Control, Quantitative RT-PCR, MTT Assay, Colony Assay, Staining, Wound Healing Assay, Flow Cytometry, Negative Control, Small Interfering RNA, Real-time Polymerase Chain Reaction