Chrabaszcz Karolina, Kaminska Katarzyna, Song Cai Li, Morikawa Junko, Kujdowicz Monika, Michalczyk Ewelina, Smeda Marta, Stojak Marta, Jasztal Agnieszka, Kazarian Sergei G, Malek Kamilla
Faculty of Chemistry, Jagiellonian University, Gronostajowa 2 St., 30-387 Krakow, Poland.
Jagiellonian Centre for Experimental Therapeutics, Jagiellonian University, Bobrzynskiego 14 St., 30-384 Krakow, Poland.
Cancers (Basel). 2021 Jan 6;13(2):162. doi: 10.3390/cancers13020162.
The current understanding of mechanisms underlying the formation of metastatic tumors has required multi-parametric methods. The tissue micro-environment in secondary organs is not easily evaluated due to complex interpretation with existing tools. Here, we demonstrate the detection of structural modifications in proteins using emerging Fourier Transform Infrared (FTIR) imaging combined with light polarization. We investigated lungs affected by breast cancer metastasis in the orthotopic murine model from the pre-metastatic phase, through early micro-metastasis, up to an advanced phase, in which solid tumors are developed in lung parenchyma. The two IR-light polarization techniques revealed, for the first time, the orientational ordering of proteins upon the progression of pulmonary metastasis of breast cancer. Their distribution was complemented by detailed histological examination. Polarized contrast imaging recognised tissue structures of lungs and showed deformations in protein scaffolds induced by inflammatory infiltration, fibrosis, and tumor growth. This effect was recognised by not only changes in absorbance of the spectral bands but also by the band shifts and the appearance of new signals. Therefore, we proposed this approach as a useful tool for evaluation of progressive and irreversible molecular changes that occur sequentially in the metastatic process.
目前对转移性肿瘤形成机制的理解需要多参数方法。由于现有工具的解释复杂,二级器官中的组织微环境不易评估。在这里,我们展示了使用新兴的傅里叶变换红外(FTIR)成像结合光偏振来检测蛋白质中的结构修饰。我们在原位小鼠模型中研究了受乳腺癌转移影响的肺,从转移前期、早期微转移到晚期,即肺实质中形成实体瘤的阶段。这两种红外光偏振技术首次揭示了乳腺癌肺转移进展过程中蛋白质的取向有序性。它们的分布通过详细的组织学检查得到补充。偏振对比成像识别出肺的组织结构,并显示出由炎症浸润、纤维化和肿瘤生长引起的蛋白质支架变形。这种效应不仅通过光谱带吸光度的变化来识别,还通过谱带位移和新信号的出现来识别。因此,我们提出这种方法是评估转移过程中依次发生的渐进性和不可逆分子变化的有用工具。