Figure 3.
Inhibition of GOLM1 expression in ALK+ ALCL cells reduces cell viability. (A) Establishment of GOLM1 stable knockdown in ALK+ALCL (SUDHL-1, SUP-M2, and Karpas 299) and Jurkat cells. Cells were infected by lentivirus-encoded GOLM1 or scramble shRNA, and stable clones were selected. The GOLM1 mRNA and (B) protein were detected by qPCR or western blotting (∗P < .05, ∗∗∗P < .001, 2-tailed Student t test). (C) The growth curves of GOLM1 knockdown ALK+ ALCL cells and (D) NA or KD expressing ALK- cells. The shGOLM1 or shscramble ALK+ ALCL cells were seeded as 1 × 105 per well (200 μL) for expansion. The cells were counted and seeded as 1 × 105 per well (200 μL) every other day during 8 or 10 days period. (E) The viability of GOLM1 knockdown ALK+ ALCL cells and (F) NA or KD expressing ALK- ALCL cells. The cells were seeded as 1 × 105 per well (200 μL). Cell viability was determined by trypan blue staining.

Inhibition of GOLM1 expression in ALK+ ALCL cells reduces cell viability. (A) Establishment of GOLM1 stable knockdown in ALK+ALCL (SUDHL-1, SUP-M2, and Karpas 299) and Jurkat cells. Cells were infected by lentivirus-encoded GOLM1 or scramble shRNA, and stable clones were selected. The GOLM1 mRNA and (B) protein were detected by qPCR or western blotting (∗P < .05, ∗∗∗P < .001, 2-tailed Student t test). (C) The growth curves of GOLM1 knockdown ALK+ ALCL cells and (D) NA or KD expressing ALK- cells. The shGOLM1 or shscramble ALK+ ALCL cells were seeded as 1 × 105 per well (200 μL) for expansion. The cells were counted and seeded as 1 × 105 per well (200 μL) every other day during 8 or 10 days period. (E) The viability of GOLM1 knockdown ALK+ ALCL cells and (F) NA or KD expressing ALK- ALCL cells. The cells were seeded as 1 × 105 per well (200 μL). Cell viability was determined by trypan blue staining.

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