“…TGFBR3 inhibits breast cancer progression through TGF-beta signaling (Lee et al, 2010). In addition, other molecules in module 1 such as ADAMTS5 (Fontanil et al, 2017), ARHGAP20 (Asaduzzaman et al, 2017), C2orf88 (Lo et al, 2015), EZH1 (Liu et al, 2012), FAM13A (Goto-Yamaguchi et al, 2018), FGF1 (Slattery et al, 2013), GNAL (Yi et al, 2009), GRAMD3 (Boiles et al, 2015), PELI2 (Zang et al, 2017), PLSCR4 (Sahay et al, 2015), PTPN14 (Belle et al, 2015), RBMS3 (Zhu et al, 2019a), SH3BGRL2 (Alexe et al, 2007;Wen et al, 2018), let-7c (Fu et al, 2017), mir-100 (Jiang et al, 2016b), mir-10b (Wang et al, 2016b), mir-125b (Wang et al, 2019a), mir-139 (Dai et al, 2017), and mir-21 (Yan et al, 2008;Yanwirasti and Arisanty, 2017;Zhu et al, 2019b) have been reported to play important roles in breast cancer. Module 2 had nine nodes, including two miRNAs, five lncRNAs, and two protein-coding genes.…”