BISPR promoted the development of TPC cells by inhibiting miR-21-5p
expression. (a) Compared with miR-NC group, the expression level of
miR-21-5p in miR-21-5p mimics group was much higher and that in
miR-21-5p inhibitor group was much lower. At the meantime, miR-21-5p
expression in sh-BISPR + miR-21-5p inhibitor group was much higher than
that in miR-21-5p inhibitor group. (b) The iodine uptake of BHT101 and
Hth83 cell lines with miR-21-5p mimics was much higher than that in
miR-NC group, while that with miR-21-5p inhibitor was lower than that in
the miR-NC group. At the same time, the cell iodine uptake in
sh-BISPR + miR-21-5p inhibitor group was much higher than that in
miR-21-5p inhibitor group. *P < 0.05, compared with miR-NC group; #P < 0.05, compared with miR-21-5p inhibitor
group. (c and d) The cell viability of BHT101 and Hth83 cell lines with
miR-21-5p mimics was much lower than that in miR-NC group, while that
with miR-21-5p inhibitor was higher than that in miR-NC group. However,
cell viability in sh-BISPR + miR-21-5p inhibitor group was lower than
that in miR-21-5p inhibitor group. *P < 0.05, compared with miR-NC group;
**P < 0.01, compared
with miR-NC group; #P < 0.05, compared with miR-21-5p inhibitor group. (e) The
number of invasive cells in BHT101 and Hth83 cell lines with miR-21-5p
mimics was much lower than that in miR-NC group while that with
miR-21-5p inhibitor was higher than that in the miR-NC group. However,
the number of invasive cells in sh-BISPR + miR-21-5p inhibitor group was
lower than that in miR-21-5p inhibitor group. *P < 0.05, compared with miR-NC group;
#P < 0.05, compared with
miR-21-5p inhibitor group.