Department of Interventional Radiology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Department of Intensive Care Unit, The First Hospital of Jilin University, Changchun, Jilin, China.
J Cell Mol Med. 2019 Jul;23(7):4523-4533. doi: 10.1111/jcmm.14342. Epub 2019 May 2.
Increased Six1 expression is commonly observed in a variety of cancers and is positively correlated with cancer progression and metastasis. Nevertheless, the mechanism by which Six1 affects the development of hepatocellular carcinoma (HCC) is still unclear. A series of experiments involving cell counting kit-8, colony formation and Transwell assay was used to determine cell proliferation, migration and invasion respectively. Histological examination and immunofluorescence assay were also performed. The messenger RNA and protein expression of interesting genes were determined by real-time reverse transcription-polymerase chain reaction and western blotting respectively. We found that Six1 was up-regulated in HCC and was associated with worse histological grade and poor survival rate. Increased expression of Six1 was shown to be able to boost cell growth, invasion, migration and epithelial-mesenchymal transition (EMT), whereas silencing of Six1 suppressed these malignant phenotypes. Mechanistic investigations revealed that, in macrophages, matrix metalloproteinase 9 (MMP-9) was up-regulated by Six1. Interestingly, Six1 expression in macrophages was also able to trigger MMP-9 induction in HCC cells. Moreover, macrophage Six1 expression was able to induce interleukin-6 (IL-6) up-regulation and increase the activity of signal transducer and activator of transcription 3 (STAT3) in HCC cells, which accounted for the elevated levels of MMP-9 and the higher invasive levels seen in HCC. Increased expression of Six1 in HCC aggravates the malignant behaviour of cancer cells, and we provide novel evidence that macrophage Six1 can stimulate cancer cell invasion by elevating MMP-9 expression.
Six1 表达增加通常在各种癌症中观察到,并且与癌症的进展和转移呈正相关。然而,Six1 影响肝细胞癌(HCC)发展的机制尚不清楚。一系列涉及细胞计数试剂盒-8、集落形成和 Transwell 分析的实验分别用于确定细胞增殖、迁移和侵袭。还进行了组织学检查和免疫荧光分析。通过实时逆转录-聚合酶链反应和蛋白质印迹分别确定了感兴趣基因的信使 RNA 和蛋白表达。我们发现 Six1 在 HCC 中上调,与较差的组织学分级和较差的生存率相关。Six1 的表达增加能够促进细胞生长、侵袭、迁移和上皮间质转化(EMT),而 Six1 的沉默则抑制这些恶性表型。机制研究表明,在巨噬细胞中,基质金属蛋白酶 9(MMP-9)被 Six1 上调。有趣的是,巨噬细胞中的 Six1 表达也能够触发 HCC 细胞中 MMP-9 的诱导。此外,巨噬细胞中的 Six1 表达能够诱导白细胞介素 6(IL-6)的上调,并增加 HCC 细胞中信号转导和转录激活因子 3(STAT3)的活性,这解释了 MMP-9 水平升高和 HCC 细胞侵袭水平升高的原因。HCC 中 Six1 的表达增加加重了癌细胞的恶性行为,我们提供了新的证据表明,巨噬细胞中的 Six1 通过上调 MMP-9 表达来刺激癌细胞的侵袭。