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. 2019 May 1;27(1):55–70. doi: 10.1038/s41418-019-0339-0

Fig. 2.

Fig. 2

Targeting JOSD1 significantly suppresses gynaecological cancer growth in vivo. ad In vivo growth and tumour weights of xenografts generated from A2780 (n = 6 for each group) and HeLa (n = 8 for each group) cells expressing either short hairpin RNAs (shRNAs) targeting JOSD1 or nontargeting shRNA. e In vitro growth of eight gynaecological cancer primary cell lines transfected with either small interfering RNAs targeting JOSD1 or negative control siRNA. f Tumour weights of ovarian cancer patient-derived xenograft models administered adeno-associated virus (AAV) targeting JOSD1 or AAV with a nontargeting sequence (n = 5 per group). Two-tailed Student’s t test; *p < 0.05, **p < 0.01 and ****p < 0.0001. For ad and f, the data are presented as the mean ± SEM. For e, the data are presented as the mean ± SD, and representative results of three biological replicates are shown