Vargas-Villarreal Javier, Cruz-Ramos Marlid, Espino-Ojeda Alba, Gutierrez-Hermosillo Hugo, Díaz De Leon-Gonzalez Enrique, Monsivais-Diaz Ofelia, Palacios-Corona Rebeca, Martinez-Armenta Carlos Alejandro, González-Salazar Francisco, Moreno-Treviño Maria Guadalupe, Guzman-De La Garza Francisco Javier
Centro de Investigación Biomedica del Noreste, Instituto Mexicano del Seguro Social, Monterrey, Nuevo Leon 64720, Mexico.
Basic Sciences Department, School of Medicine, University of Monterrey, San Pedro Garza García, Nuevo Leon 66238, Mexico.
Mol Clin Oncol. 2021 May;14(5):106. doi: 10.3892/mco.2021.2268. Epub 2021 Mar 20.
Malignant ascites (MA) and malignant pleural effusion (MPE) are frequently developed in patients with metastatic cancer; however, the biological properties of these fluids have not been clarified. The present study explored the biological role of a low molecular fraction derived from malignant effusions on the activation of peripheral blood mononuclear cells and on the proliferation of breast cancer cells and fibroblast 55x cells. A <10-kDa fraction from effusions of 41 oncological patients and 34 individuals without cancer was purified, and its potential role in inhibiting nitric oxide (NO) production on lipopolysaccharide (LPS)-stimulated peripheral blood mononuclear cells was explored, as well as its cytotoxicity on MCF-7 breast cancer cells and fibroblast 55x cells. A significant decrease in NO production was observed in the <10-kDa fraction from malignant effusions. In addition, the acellular fraction from MA decreased the viability of breast cancer cells without affecting human fibroblasts. These data support the presence of low molecular weight molecules in malignant samples with a specific role in inhibiting the defense mechanisms of peripheral blood mononuclear cells and decreasing the viability of breast cancer cells .
恶性腹水(MA)和恶性胸腔积液(MPE)在转移性癌症患者中经常出现;然而,这些液体的生物学特性尚未阐明。本研究探讨了源自恶性积液的低分子组分对人外周血单个核细胞激活以及乳腺癌细胞和成纤维细胞55x细胞增殖的生物学作用。对41例肿瘤患者和34例非癌症个体的积液中<10 kDa的组分进行了纯化,并探讨了其对脂多糖(LPS)刺激的外周血单个核细胞中一氧化氮(NO)产生的抑制作用及其对MCF-7乳腺癌细胞和成纤维细胞55x细胞的细胞毒性。在恶性积液的<10 kDa组分中观察到NO产生显著减少。此外,MA的无细胞组分降低了乳腺癌细胞的活力,而不影响人成纤维细胞。这些数据支持恶性样本中存在低分子量分子,其在抑制外周血单个核细胞的防御机制和降低乳腺癌细胞活力方面具有特定作用。