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. 2019 May 1;12(6):859–870. doi: 10.1016/j.tranon.2019.03.005

Supplementary Figure S5.

Supplementary Figure S5

Biologic effects of metadherin suppression in MPM cells.

(A) MTDH knockdown (red) decreased proliferation in MPM cells. On day 3, cell proliferation decreased 47% (H2452), 17% (MSTO-211H), and 20% (H2373) (P < .05). (B) Boyden chamber assay showed that MTDH knockdown decreases invasive capability of MPM cells by 48% (H2452) and 63% (H2373). (C) MTDH knockdown abrogated colony formation. Soft agar assays reveal that relative colony numbers decreased 82% (H2452), 76% (MSTO-211H), and 53% (H2373) (P < .05). (D) Cell viability was assessed at varying concentrations of cisplatin to calculate IC50 values. MTDH knockdown (red) rendered MPM cells more chemosensitive, requiring 24% (H2452), 52% (MSTO-211H), and 70% (H2373) lower doses of drug to reach IC50 levels. (E) Levels of apoptosis were measured after MPM cells were treated with a fixed dose (IC50) of cisplatin. MTDH knockdown significantly augmented apoptosis at 48 hours by 1.5-fold (H2452), 1.2-fold (MSTO-211H), and 1.3-fold (H2373) compared to parental cells. Where applicable, data are presented as mean ± SE. Ctrl is a knockdown scrambled sample. * is P < .05 versus parent cell line and/or negative control specimen. MTDH-KD is stable gene suppression of MTDH in MPM cells.