Sun Dongying, Lei Wei, Hou Xiaodong, Li Hui, Ni Wenlu
Department of Medical Imaging, Henan University First Affiliated Hospital, Kaifeng, Henan, China,
Cancer Manag Res. 2019 Jan 17;11:821-830. doi: 10.2147/CMAR.S180242. eCollection 2019.
PUF60 is a splicing variant of far upstream element binding protein 1-interacting repressor, which is abnormally expressed in a variety of tumors and is closely involved in their progression. However, whether PUF60 participates in the occurrence and development of breast cancer remains unknown. Therefore, the objective of the current study is to explore the effects and mechanism of PUF60 in the progression of breast cancer.
PUF60 expression patterns in breast cancer tissues and cells were determined by RT-PCR and Western blotting. The relationship between PUF60 expression and patients' clinical features and outcome was evaluated to assess the potential of PUF60 as a marker for progression and prognosis prediction. CCK-8, flow cytometry, transwell and in vivo tumor formation assays were used to detect cell proliferation, apoptosis, migration, invasion and tumorigenesis. The effects of PUF60 on the activation of PTEN/PI3K/AKT were also evaluated by Western blotting and immunofluorescence assays.
The expression of PUF60 was elevated in breast cancer tissue samples and cell lines, and its high expression was closely associated with the high incidence of lymph node metastasis and advanced TNM stage. Besides, upregulation of PUF60 with lentivirus infection significantly increased the growth, migration, and invasion and repressed the apoptosis of breast cancer HCC1937 and MDA-MB-231 cells, while silencing of PUF60 with shRNA showed the opposite results. Moreover, PUF60 upregulation promoted the expression of p-AKT, PI3K, and mTOR, while decreased PTEN expression through inhibiting its stability and enhancing its ubiquitination. Furthermore, upregulation of PUF60 promoted the tumorigenesis in vivo, whereas this effect was impaired when PTEN expression was upregulated in MDA-MB-231 and HCC1937 cells.
This study demonstrates that PUF60 is highly expressed in breast cancer; upregulation of PUF60 accelerates the progression of breast cancer through PTEN inhibition.
PUF60是远上游元件结合蛋白1相互作用阻遏物的一种剪接变体,在多种肿瘤中异常表达,并密切参与其进展。然而,PUF60是否参与乳腺癌的发生和发展仍不清楚。因此,本研究的目的是探讨PUF60在乳腺癌进展中的作用及机制。
通过RT-PCR和蛋白质免疫印迹法检测乳腺癌组织和细胞中PUF60的表达模式。评估PUF60表达与患者临床特征及预后的关系,以评估PUF60作为进展和预后预测标志物的潜力。采用CCK-8法、流式细胞术、Transwell实验和体内肿瘤形成实验检测细胞增殖、凋亡、迁移、侵袭和肿瘤发生情况。还通过蛋白质免疫印迹法和免疫荧光实验评估PUF60对PTEN/PI3K/AKT激活的影响。
PUF60在乳腺癌组织样本和细胞系中表达升高,其高表达与淋巴结转移高发生率和TNM分期晚期密切相关。此外,慢病毒感染上调PUF60显著增加了乳腺癌HCC1937和MDA-MB-231细胞的生长、迁移和侵袭,并抑制了其凋亡,而shRNA沉默PUF60则显示出相反的结果。此外,PUF60上调促进了p-AKT、PI3K和mTOR的表达,同时通过抑制PTEN稳定性和增强其泛素化降低了PTEN表达。此外,PUF60上调促进了体内肿瘤发生,而在MDA-MB-231和HCC1937细胞中上调PTEN表达时,这种作用受到损害。
本研究表明PUF60在乳腺癌中高表达;PUF60上调通过抑制PTEN加速乳腺癌进展。