The Scripps Research Institute, La Jolla, CA, USA.
The New York University School of Medicine, New York, NY, USA.
Oncogene. 2018 Apr;37(14):1815-1829. doi: 10.1038/s41388-017-0075-1. Epub 2018 Jan 19.
Latent transforming growth factor β (TGFβ)-binding proteins (LTBPs) are important for the secretion, activation, and function of mature TGFβ, especially so in cancer cell physiology. However, specific roles of the LTBPs remain understudied in the context of the primary tumor microenvironment. Herein, we investigated the role of LTBP3 in the distinct processes involved in cancer metastasis. By using three human tumor cell lines of different tissue origin (epidermoid HEp-3 and prostate PC-3 carcinomas and HT-1080 fibrosarcoma) and several metastasis models conducted in both mammalian and avian settings, we show that LTBP3 is involved in the early dissemination of primary cancer cells, namely in the intravasation step of the metastatic cascade. Knockdown of LTBP3 in all tested cell lines led to significant inhibition of tumor cell intravasation, but did not affect primary tumor growth. LTBP3 was dispensable in the late steps of carcinoma cell metastasis that follow tumor cell intravasation, including vascular arrest, extravasation, and tissue colonization. However, LTBP3 depletion diminished the angiogenesis-inducing potential of HEp-3 cells in vivo, which was restorable by exogenous delivery of LTBP3 protein. A similar compensatory approach rescued the dampened intravasation of LTBP3-deficient HEp-3 cells, suggesting that LTBP3 regulates the induction of the intravasation-supporting angiogenic vasculature within developing primary tumors. Using our recently developed microtumor model, we confirmed that LTBP3 loss resulted in the development of intratumoral vessels with an abnormal microarchitecture incompatible with efficient intravasation of HEp-3 carcinoma cells. Collectively, these findings demonstrate that LTBP3 represents a novel oncotarget that has distinctive functions in the regulation of angiogenesis-dependent tumor cell intravasation, a critical process during early cancer dissemination. Our experimental data are also consistent with the survival prognostic value of LTBP3 expression in early-stage head and neck squamous cell carcinomas, further indicating a specific role for LTBP3 in cancer progression toward metastatic disease.
潜伏转化生长因子β(TGFβ)结合蛋白(LTBPs)对于成熟 TGFβ的分泌、激活和功能至关重要,尤其是在癌细胞生理学中。然而,在原发性肿瘤微环境的背景下,LTBPs 的具体作用仍未得到充分研究。在此,我们研究了 LTBP3 在癌症转移涉及的不同过程中的作用。通过使用三种不同组织来源的人肿瘤细胞系(表皮样 HEp-3 和前列腺 PC-3 癌和 HT-1080 纤维肉瘤)和几种在哺乳动物和禽类中进行的转移模型,我们表明 LTBP3 参与了原发性癌细胞的早期扩散,即在转移级联的血管内渗步骤中。在所有测试的细胞系中敲低 LTBP3 都会导致肿瘤细胞血管内渗的显著抑制,但不会影响原发性肿瘤的生长。LTBP3 在肿瘤细胞血管内渗后肿瘤细胞转移的晚期步骤中是可有可无的,包括血管阻滞、血管外渗和组织定植。然而,LTBP3 耗竭会减少 HEp-3 细胞在体内的血管生成诱导潜力,而外源性递送 LTBP3 蛋白可以恢复这一潜力。类似的补偿方法挽救了 LTBP3 缺陷型 HEp-3 细胞的血管内渗能力下降,表明 LTBP3 调节在发育中的原发性肿瘤内诱导支持血管内渗的血管生成血管。使用我们最近开发的微肿瘤模型,我们证实 LTBP3 缺失导致肿瘤内血管的发育具有异常的微结构,与 HEp-3 癌细胞的有效血管内渗不兼容。总的来说,这些发现表明 LTBP3 是一种新的癌基因靶点,在调节依赖血管生成的肿瘤细胞血管内渗方面具有独特的功能,这是早期癌症扩散过程中的一个关键过程。我们的实验数据也与早期头颈部鳞状细胞癌中 LTBP3 表达的生存预后价值一致,进一步表明 LTBP3 在癌症向转移性疾病进展中的特定作用。