Mohammed Sulma I, Torres-Luquis Odalys, Zhou Weidong, Lanman Nadia Attalah, Espina Virginia, Liotta Lance
Department of Comparative Pathobiology, Purdue University, West Lafayette, IN 47907, USA.
Purdue University Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Breast Cancer (Dove Med Press). 2020 Mar 25;12:57-67. doi: 10.2147/BCTT.S236168. eCollection 2020.
During metastasis, tumor cells metastasize from primary tumors to distant organs via the circulatory and the lymphatic systems. There is a plethora of information about metastasis through the circulatory system, however not much information is available about the tumor cells dissemination through the lymphatic system or the lymphatic microenvironment that aids in this process in breast cancer metastasis.
The study designed to examine the tumor-derived secretome in lymph before reaching the draining lymph nodes.
Using a microsurgical technique, we have collected the lymph in transit from the primary tumor en route to the regional lymph node in animals with metastatic and non-metastatic mammary carcinoma and healthy controls. The lymph samples were subjected to LC-MS/MS analysis, bioinformatics, and pathway analysis.
The metastatic tumor-draining lymph before its entry into the closest regional lymph node contain 26 proteins with >175-folds in abundance compared to lymph from non-metastatic tumor-bearing animals. Among these proteins were biliverdin reductase B, heat shock protein, coagulation factor XIII, lymphocytes cytosol protein 1, and aldose reductase. These proteins were not identified in the lymph from healthy animals. Pathways analysis revealed that cadherin-mediated endocytosis, acute phase response, junction signaling, gap junction, VEGF singling, and PI3K/AKT singling pathways are overrepresented in the lymph from metastatic tumor-bearing compared to the lymph from non-metastatic tumor-bearing animals. Among the significantly up-regulated proteins in the lymph from metastatic tumor-bearing animals were proteins that identified in exosomes include heat shock protein, enolase 1 alpha, S100, and biliverdin reductase B. One of the proteins significantly down-regulated in lymph from animals with metastasis is Kininogen, a known metastasis inhibitor protein.
Proteins and exosomal proteins in lymph draining a metastatic tumor are different from those in lymph draining non-metastatic tumors, and these proteins involved in pathways that regulate tumor cells migration and invasion.
在转移过程中,肿瘤细胞通过循环系统和淋巴系统从原发性肿瘤转移至远处器官。关于通过循环系统转移的信息众多,但关于肿瘤细胞通过淋巴系统的播散或在乳腺癌转移过程中辅助此过程的淋巴微环境的信息却不多。
本研究旨在检测肿瘤引流至引流淋巴结之前的淋巴液中的肿瘤来源分泌组。
我们采用显微外科技术,收集了患有转移性和非转移性乳腺癌的动物以及健康对照动物从原发性肿瘤至区域淋巴结途中的转运淋巴液。对淋巴液样本进行液相色谱-串联质谱分析、生物信息学分析和通路分析。
与来自非转移性荷瘤动物的淋巴液相比,转移性肿瘤引流至最近区域淋巴结之前的淋巴液中含有26种丰度增加超过175倍的蛋白质。这些蛋白质包括胆红素还原酶B、热休克蛋白、凝血因子XIII、淋巴细胞胞质蛋白1和醛糖还原酶。这些蛋白质在健康动物的淋巴液中未被鉴定出。通路分析显示,与非转移性荷瘤动物的淋巴液相比,转移性荷瘤动物的淋巴液中钙黏蛋白介导的内吞作用、急性期反应、连接信号传导、缝隙连接、血管内皮生长因子信号传导和PI3K/AKT信号传导通路的富集程度更高。在转移性荷瘤动物的淋巴液中显著上调的蛋白质中,有一些在细胞外泌体中鉴定出的蛋白质,包括热休克蛋白、烯醇化酶1α、S100和胆红素还原酶B。在有转移的动物的淋巴液中显著下调的一种蛋白质是激肽原,一种已知的转移抑制蛋白。
转移性肿瘤引流淋巴液中的蛋白质和细胞外泌体蛋白质与非转移性肿瘤引流淋巴液中的不同,且这些蛋白质参与调节肿瘤细胞迁移和侵袭的通路。