Figure 6.
PRC1 contributes to BC by inhibiting expression of BC tumor suppressors. CFAs of K562 and KCL22 cells retrovirally transduced with (A) EGR1, either wild-type (WT) or dominant negative (DN) or (C) the indicated cDNAs are shown. (A) *P = .001; **P = .00004; #P = .03; ##P = .04. (C) *P = .000001; **P = .0011; #P = .000003; ##P = .003. CFAs of K562, KCL22 (E), and primary BC cells (G) retrovirally transduced with FLAG-NR4A2, either wild-type (WT) or (C283G) mutant are shown. (E) *P = .0009; **P = .0022; #P = .027. (G) *P = .0021. For panels A, C, E, and G, results are given as mean ± standard deviation (n = 3). For each CFA plot, the corresponding immunoblots are shown on the right (B,D,F,H). Control, cells retrovirally transduced with empty vector.

PRC1 contributes to BC by inhibiting expression of BC tumor suppressors. CFAs of K562 and KCL22 cells retrovirally transduced with (A) EGR1, either wild-type (WT) or dominant negative (DN) or (C) the indicated cDNAs are shown. (A) *P = .001; **P = .00004; #P = .03; ##P = .04. (C) *P = .000001; **P = .0011; #P = .000003; ##P = .003. CFAs of K562, KCL22 (E), and primary BC cells (G) retrovirally transduced with FLAG-NR4A2, either wild-type (WT) or (C283G) mutant are shown. (E) *P = .0009; **P = .0022; #P = .027. (G) *P = .0021. For panels A, C, E, and G, results are given as mean ± standard deviation (n = 3). For each CFA plot, the corresponding immunoblots are shown on the right (B,D,F,H). Control, cells retrovirally transduced with empty vector.

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