Department of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Department of Pathology, Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Thorac Cancer. 2021 Jan;12(1):79-89. doi: 10.1111/1759-7714.13715. Epub 2020 Oct 29.
Transmembrane protein 107 (TMEM107) is a key regulator of the cilium composition and Hedgehog signaling. Lower TMEM107 gene copies are correlated with poor prognosis in non-small cell lung carcinoma (NSCLC). However, TMEM107 protein expression, localization, and function in NSCLC remain unclear.
We first evaluated TMEM107 expression in 12 newly diagnosed cases of NSCLC and paired adjacent healthy tissues by western blotting. We then used an immunohistochemical method to detect TMEM107 expression in 106 paraffin-embedded NSCLC and corresponding normal samples and analyzed its relationship with clinicopathological parameters. Moreover, we determined the impact of TMEM107 upregulation and downregulation on invasion, EMT and Hedgehog pathway in NSCLC cells.
Our results showed that TMEM107 is localized in the cytoplasm and that its expression was lower in NSCLC. TMEM107 expression was positively correlated with cell differentiation and negatively correlated with lymph node metastasis. In A549 and HCC460 cells, downregulation of TMEM107 facilitated cell invasion and upregulated the expression of the Hedgehog pathway target protein Gli1, invasion-associated proteins N-cadherin, vimentin, MMP2, and MMP9, and epithelial-mesenchymal transition (EMT), and inhibited the expression of E-cadherin. Treatment with the Hedgehog pathway inhibitor GANT61 attenuated TMEM107-knockdown-induced EMT and invasiveness.
These results indicate that TMEM107 inhibits EMT and invasion by negatively regulating Hedgehog signaling and that it is downregulated in NSCLC.
TMEM107 expression is lower in NSCLC tissues and correlates with poor prognosis TMEM107 inhibits invasion of NSCLC cells TMEM107 inhibits EMT of NSCLC cells Downregulation of TMEM107 activates the Hedgehog signaling pathway Downregulation of TMEM107 promotes EMT and migration in NSCLC by activating the Hedgehog signaling pathway.
跨膜蛋白 107(TMEM107)是纤毛组成和 Hedgehog 信号的关键调节因子。TMEM107 基因拷贝数较低与非小细胞肺癌(NSCLC)的预后不良相关。然而,TMEM107 蛋白在 NSCLC 中的表达、定位和功能仍不清楚。
我们首先通过 Western blot 评估了 12 例新诊断的 NSCLC 患者及其配对的相邻健康组织中 TMEM107 的表达。然后,我们使用免疫组织化学方法检测了 106 例石蜡包埋的 NSCLC 及其相应正常样本中的 TMEM107 表达,并分析了其与临床病理参数的关系。此外,我们还确定了 TMEM107 上调和下调对 NSCLC 细胞侵袭、上皮间质转化和 Hedgehog 通路的影响。
我们的结果表明,TMEM107 定位于细胞质,在 NSCLC 中表达较低。TMEM107 表达与细胞分化呈正相关,与淋巴结转移呈负相关。在 A549 和 HCC460 细胞中,下调 TMEM107 促进了细胞侵袭,并上调了 Hedgehog 通路靶蛋白 Gli1、侵袭相关蛋白 N-钙粘蛋白、波形蛋白、MMP2 和 MMP9 的表达,以及上皮间质转化(EMT),并抑制了 E-钙粘蛋白的表达。用 Hedgehog 通路抑制剂 GANT61 处理可减弱 TMEM107 敲低诱导的 EMT 和侵袭性。
这些结果表明,TMEM107 通过负向调节 Hedgehog 信号抑制 EMT 和侵袭,并且在 NSCLC 中下调。
TMEM107 在 NSCLC 组织中的表达较低,与预后不良相关 TMEM107 抑制 NSCLC 细胞的侵袭 TMEM107 抑制 NSCLC 细胞的 EMT TMEM107 下调激活 Hedgehog 信号通路 TMEM107 下调通过激活 Hedgehog 信号通路促进 NSCLC 中的 EMT 和迁移。