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B4GALNT1 induces angiogenesis, anchorage independence growth and motility, and promotes tumorigenesis in melanoma by induction of ganglioside GM2/GD2.

B4GALNT1 通过诱导神经节苷脂GM2/gd2 诱导黑色素瘤血管生成、锚定独立性生长和运动,并促进肿瘤发生。

  • 影响因子:4.29
  • DOI:10.1038/s41598-019-57130-2
  • 作者列表:"Yoshida H","Koodie L","Jacobsen K","Hanzawa K","Miyamoto Y","Yamamoto M
  • 发表时间:2020-01-27
Abstract

:β-1,4-N-Acetyl-Galactosaminyltransferase 1 (B4GALNT1) encodes the key enzyme B4GALNT1 to generate gangliosides GM2/GD2. GM2/GD2 gangliosides are surface glycolipids mainly found on brain neurons as well as peripheral nerves and skin melanocytes and are reported to exacerbate the malignant potential of melanomas. In order to elucidate the mechanism, we performed functional analyses of B4GALNT1-overexpressing cells. We analyzed ganglioside pattern on four melanoma and two neuroblastoma cell lines by high performance liquid chromatography (HPLC). We overexpressed B4GALNT1 in GM2/GD2-negative human melanoma cell line (SH4) and confirmed production of GM2/GD2 by HPLC. They showed higher anchorage independence growth (AIG) in colony formation assay, and exhibited augmented motility. In vitro, cell proliferation was not affected by GM2/GD2 expression. In vivo, GM2/GD2-positive SH4 clones showed significantly higher tumorigenesis in NOD/Scid/IL2Rγ-null mice, and immunostaining of mouse CD31 revealed that GM2/GD2 induced remarkable angiogenesis. No differences were seen in melanoma stem cell and Epithelial-Mesenchymal Transition markers between GM2/GD2-positive and -negative SH4 cells. We therefore concluded that B4GALNT1, and consequently GM2/GD2, enhanced tumorigenesis via induction of angiogenesis, AIG, and cell motility. RNA-Seq suggested periostin as a potential key factor for angiogenesis and AIG. These findings may lead to development of novel therapy for refractory melanoma.

摘要

: Β-1,4-n-乙酰-半乳糖胺基转移酶 1 (B4GALNT1) 编码关键酶B4GALNT1,生成神经节苷脂GM2/gd2。GM2/GD2 神经节苷脂是主要存在于大脑神经元以及周围神经和皮肤黑色素细胞上的表面糖脂,据报道可加剧黑色素瘤的恶性潜能。为了阐明其作用机制,我们对B4GALNT1-overexpressing细胞进行了功能分析。我们通过高效液相色谱 (HPLC) 分析了四种黑色素瘤和两种神经母细胞瘤细胞系上的神经节苷脂模式。我们在GM2/GD2-negative人黑色素瘤细胞系 (SH4) 中过表达了B4GALNT1,并通过HPLC证实了GM2/GD2 的产生。他们在集落形成试验中表现出更高的锚定独立性生长 (AIG),并表现出增强的运动性。在体外,细胞增殖不受GM2/GD2 表达的影响。在体内,GM2/GD2-positive SH4 克隆在NOD/Scid/il2r γ 缺失小鼠中表现出显著的肿瘤发生,小鼠CD31 的免疫染色显示GM2/GD2 诱导了显著的血管生成。GM2/GD2-positive和阴性SH4 细胞的黑色素瘤干细胞和上皮间质转化标志物未见差异。因此,我们得出结论,B4GALNT1,以及GM2/GD2,通过诱导血管生成、AIG和细胞运动增强了肿瘤发生。RNA-Seq建议骨膜蛋白作为血管生成和AIG的潜在关键因子。这些发现可能导致难治性黑色素瘤新疗法的发展。

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影响因子:0.96
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皮肤肿瘤方向

皮肤肿瘤是发生在皮肤的细胞增生性疾病,是一种常见病。发生于皮内或皮下组织的新生物,种类很多,临床上分良性肿瘤和恶性肿瘤。恶性肿瘤可以不断增殖,引起转移,威胁生命,称为皮肤癌。

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